prem14a
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
SCHEDULE 14A
INFORMATION
PROXY STATEMENT PURSUANT TO SECTION 14(a) OF
THE SECURITIES EXCHANGE ACT OF 1934
Filed by the Registrant þ
Filed by a party other than the
Registrant o
Check the appropriate box:
þ Preliminary
Proxy Statement
o Confidential, for Use
of the Commission Only (as permitted by
Rule 14a-6(e)(2))
o Definitive Proxy
Statement
o Definitive Additional
Materials
o Soliciting Material
Pursuant to
§240.14a-12
LIGAND PHARMACEUTICALS INCORPORATED
(Name of Registrant as Specified In
Its Charter)
(Name of Person(s) Filing Proxy
Statement, if other than the Registrant)
Payment of Filing Fee (Check the appropriate box):
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o
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No fee required.
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þ
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Fee computed on table below per Exchange Act
Rules 14a-6(i)(1)
and 0-11.
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1)
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Title of each class of securities to which transaction applies:
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2)
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Aggregate number of securities to which transaction applies:
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3)
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Per unit price or other underlying value of transaction computed
pursuant to Exchange Act
Rule 0-11
(set forth the amount on which the filing fee is calculated and
state how it was determined):
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The purchase price payable under the asset purchase agreement
consists of an aggregate upfront cash consideration of
$265 million, assumption by King of payment obligations of
Ligand of $47.75 million (or reimbursement to Ligand at
closing of the asset sale to the extent any such amounts have
been paid) and specified existing royalty obligations to third
parties, and receipt of certain royalty payments based on
Kings annual net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017.
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Solely for purposes of calculating the amount of the filing fee,
the registrant estimates a purchase price of approximately
$480.8 million.
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4)
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Proposed maximum aggregate value of transaction:
$480.8 million
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5)
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Total fee paid: $51,445.60
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o
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Fee paid previously with preliminary materials.
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Check box if any part of the fee is offset as provided by
Exchange Act
Rule 0-11(a)(2)
and identify the filing for which the offsetting fee was paid
previously. Identify the previous filing by registration
statement number, or the Form or Schedule and the date of its
filing.
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(1)
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Amount Previously Paid: $
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(2)
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Form, Schedule or Registration Statement No.:
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PRELIMINARY COPY SUBJECT TO
COMPLETION
DATED ,
2006
Ligand Pharmaceuticals
Incorporated
10275 Science Center Drive
San Diego, California 92121
,
2006
To our stockholders:
You are cordially invited to attend a special meeting of
stockholders of Ligand Pharmaceuticals Incorporated to be held
at the La Jolla Marriott located at 4240 La Jolla
Village Drive, La Jolla, California 92037
on ,
2006 at 9:00 a.m., local time.
We have agreed to sell all of our rights in and to
AVINZA®
(morphine sulfate extended-release capsules), in the United
States, its territories and Canada to King Pharmaceuticals, Inc.
(King), and its wholly-owned subsidiary King
Pharmaceuticals Research and Development, Inc. (King
R&D), pursuant to an asset purchase agreement, dated
as of September 6, 2006. In exchange for our rights in and
to
AVINZA®,
King and King R&D have agreed to pay us $265 million in
cash, subject to specific inventory adjustments, assume a
payment obligation of Ligand of approximately $48 million
(or reimburse Ligand at closing of the asset sale to the extent
any such amounts have been paid ) and specified existing royalty
obligations to third parties, and pay Ligand certain royalty
payments based on Kings annual net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017. The full text of the asset
purchase agreement is included as Annex A to the proxy
statement that accompanies this letter.
The proposed asset sale will not become effective until such
time as we receive not less than the minimum number of votes
necessary to approve the sale of all or substantially all of our
assets, under Delaware law. We have scheduled a special meeting
of our stockholders for this vote
on ,
2006. YOUR VOTE IS VERY IMPORTANT.
After careful consideration, our board of directors has
unanimously determined that the proposed sale of assets is in
the best interest of Ligand Pharmaceuticals Incorporated and our
stockholders. THE BOARD OF DIRECTORS UNANIMOUSLY APPROVED THE
PROPOSED SALE AND THE ASSET PURCHASE AGREEMENT AND RECOMMENDS
THAT YOU VOTE FOR THE APPROVAL AND ADOPTION OF THE
PROPOSED SALE.
We are also asking for your approval of a proposal to amend
Ligands 2002 Stock Incentive Plan (the 2002
Plan) to allow equitable adjustments to be made to options
outstanding under the 2002 Plan in the event of a payment of a
special cash dividend to our stockholders.
Our board of directors has approved the amendment to the 2002
Plan. THE BOARD OF DIRECTORS RECOMMENDS THAT YOU VOTE FOR THE
APPROVAL AND ADOPTION OF THE AMENDMENTS TO OUR 2002 PLAN.
Please review in detail the attached proxy statement for a more
complete statement regarding the proposal to approve the asset
sale (proposal 1 in this proxy statement), which includes a
description of the asset purchase agreement, the background of
the decision to enter into the asset purchase agreement, and the
reasons that our board of directors has decided to recommend
that you approve the asset sale; and the amendment to the 2002
Plan (proposal 2 in this proxy statement).
Your vote is very important to us regardless of the number of
shares you own. Whether or not you are able to attend the
special meeting in person, please complete, sign and date the
enclosed proxy card and return it in the envelope provided as
soon as possible. If you hold shares of our common stock
directly in your name, you may also grant a proxy using the
Internet or by telephone by following the instructions printed
on your proxy card. Granting a
proxy by mail, telephone or the Internet will not limit your
right to vote in person if you wish to attend the special
meeting and vote in person.
On behalf of our board of directors, I thank you for your
support and urge you to vote FOR each of the
proposals described in this proxy statement.
By Order of the Board of Directors,
Henry F. Blissenbach
Chairman and Interim Chief Executive Officer
San Diego, California
,
2006
The notice and proxy statement are first being mailed to our
stockholders on or
about ,
2006.
Ligand Pharmaceuticals
Incorporated
10275 Science Center Drive
San Diego, California 92121
NOTICE OF SPECIAL MEETING OF
STOCKHOLDERS
To Be Held
On ,
2006
To our stockholders:
A special meeting of stockholders of Ligand Pharmaceuticals
Incorporated will be held at the La Jolla Marriott located
at 4240 La Jolla Village Drive, La Jolla, California
92037
on ,
2006 at 9:00 a.m., local time. At this meeting you will be
asked:
1. To consider and to vote on a proposal to approve the
sale of all or substantially all of our assets under Delaware
law through the sale of our rights in and to
AVINZA®
(morphine sulfate extended-release capsules), in the United
States, its territories and Canada, pursuant to the asset
purchase agreement attached as Annex A to this proxy
statement;
2. To consider and to vote on a proposal to amend
Ligands 2002 Stock Incentive Plan to allow equitable
adjustments to be made to options outstanding under the plan in
the event of the payment of a large non-recurring cash dividend;
3. To approve adjournment of the special meeting, if
necessary, to facilitate the approval of the preceding
proposals, including to permit the solicitation of additional
proxies if there are not sufficient votes at the time of the
special meeting to establish a quorum or to approve the
preceding proposals; and
4. To transact such other business as may properly be
brought before the special meeting or any adjournment or
postponement thereof.
After careful consideration, our board of directors has
unanimously determined that the proposed sale of assets is in
the best interest of Ligand Pharmaceuticals Incorporated and our
stockholders. THE BOARD OF DIRECTORS UNANIMOUSLY APPROVED THE
PROPOSED SALE AND THE ASSET PURCHASE AGREEMENT AND RECOMMENDS
THAT YOU VOTE FOR THE APPROVAL AND ADOPTION OF THE
PROPOSED SALE.
Our board of directors has approved the amendment to our 2002
Stock Incentive Plan. THE BOARD OF DIRECTORS RECOMMENDS THAT
YOU VOTE FOR THE APPROVAL AND ADOPTION OF THE AMENDMENT TO THE
2002 STOCK INCENTIVE PLAN.
Only holders of record of our common stock at the close of
business
on ,
2006, will be entitled to notice of and to vote at the special
meeting or any adjournment thereof. Each share of our common
stock is entitled to one vote on each matter to be voted upon at
the special meeting.
Your vote is important, regardless of the number of shares you
own. The proposed sale of
AVINZA®
will not be completed unless it is authorized by the affirmative
vote of the holders of a majority of the outstanding shares of
our common stock entitled to vote at the special meeting. Even
if you plan to attend the meeting in person, we request that you
complete, sign, date and return the enclosed proxy or grant a
proxy by the telephone or using the Internet to ensure that your
shares will be represented at the meeting if you are unable to
attend. Your prompt cooperation will be greatly appreciated.
You are urged to review carefully the information contained in
the enclosed proxy statement prior to deciding how to vote your
shares at the special meeting.
The notice and proxy statement are first being mailed to
stockholders on or
about ,
2006.
Please follow the voting instructions on the enclosed proxy card
to vote either by mail, telephone or electronically by the
Internet.
By Order of the Board of Directors,
Warner R. Broaddus
Secretary
San Diego, California
,
2006
TABLE OF
CONTENTS
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A-1
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B-1
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ii
SUMMARY
TERM SHEET
The following summary highlights selected information from this
proxy statement and may not contain all of the information that
may be important to you. Accordingly, we encourage you to read
carefully this entire proxy statement, its annexes and the
documents referred to in this proxy statement. Each item in this
summary includes a page reference directing you to a more
complete description of that item. In this proxy statement, the
terms Ligand, company, we,
our, ours, and us refer to
Ligand Pharmaceuticals Incorporated, a Delaware corporation, and
its subsidiaries.
Parties
to the Asset Sale
Ligand Pharmaceuticals Incorporated
10275 Science Center Drive
San Diego, California 92121
Telephone No.:
(858) 550-7500
Ligand discovers, develops and markets new drugs that address
critical unmet medical needs of patients in the areas of cancer,
pain, skin diseases, mens and womens hormone-related
diseases, osteoporosis, metabolic disorders, and cardiovascular
and inflammatory diseases. Ligands proprietary drug
discovery and development programs are based on its leadership
position in gene transcription technology, primarily related to
intracellular receptors.
King Pharmaceuticals, Inc.
501 Fifth Street
Bristol, Tennessee 37620
Telephone No.:
(423) 989-8000
King Pharmaceuticals, Inc., or King, is a vertically integrated
branded pharmaceutical company. King seeks to capitalize on
opportunities in the pharmaceutical industry through the
development, including through in-licensing arrangements and
acquisitions, of novel branded prescription pharmaceutical
products in attractive markets and the strategic acquisition of
branded products that can benefit from focused promotion and
marketing and product life-cycle management.
King Pharmaceuticals Research and Development, Inc.
4000 CentreGreen Way, Suite 300
Cary, North Carolina 27513
Telephone No.:
(919) 653-7099
King Pharmaceuticals Research and Development, Inc., or King
R&D, is a Delaware corporation and a wholly-owned subsidiary
of King.
The
Special Meeting
Date,
Time, Place and Purpose (Page 11)
The special meeting will be held
on ,
2006, starting at 9:00 a.m., local time, at the
La Jolla Marriott located at 4240 La Jolla Village
Drive, La Jolla, California 92037.
You will be asked to consider and vote upon approval of:
(i) the asset sale and adoption of the asset purchase
agreement; and (ii) the amendment of our 2002 Stock
Incentive Plan, referred to in this proxy statement as the 2002
Plan, to allow equitable adjustments to be made to options
subject to the 2002 Plan in the event of the payment of a
special cash dividend. In addition, you will be asked to approve
the adjournment of the special meeting, if necessary, in order
to permit the solicitation of additional proxies if there are
not sufficient votes at the time of the special meeting to
establish a quorum or to approve the forgoing proposals.
The persons named in the accompanying proxy card will also have
discretionary authority to vote upon other business, if any,
that properly comes before the special meeting and any
adjournment of the special meeting.
Record
Date, Voting and Quorum (Page 11)
You are entitled to vote at the special meeting if you owned
shares of our common stock at the close of business
on ,
2006, the record date for the special meeting. You will have one
vote for each share of our common stock that you owned on the
record date. As of the record date, there
were shares
of our common stock outstanding and entitled to be voted.
1
A quorum of the holders of the outstanding shares of our common
stock must be present for the special meeting to be held. A
quorum is present if the holders of a majority of the
outstanding shares of our common stock entitled to vote are
present at the special meeting, either in person or represented
by proxy. Abstentions and broker non-votes are counted as
present for the purpose of determining whether a quorum is
present. A broker non-vote occurs on an item when a broker is
not permitted to vote on that item without instructions from the
beneficial owner of the shares and no instructions are given.
Required
Vote (Page 12)
For the first proposal, the affirmative vote of the holders of a
majority of our common stock outstanding at the close of
business on the record date will be required for approval. A
failure to vote your shares, an abstention or a broker non-vote
will have the same effect as a vote against the asset sale.
For the second and third proposals, the affirmative vote of the
holders of a majority of our common stock represented in person
or by proxy at the special meeting and entitled to vote will be
required to approve each proposal. Abstentions and broker
non-votes will not be counted in determining the number of votes
present in person or represented by proxy, and therefore will
not have an effect on the approval of the amendment to the 2002
Plan or whether to adjourn the meeting. The approval of the
amendment to the 2002 Plan is not a condition to the approval of
the asset sale.
Security
Ownership of Certain Beneficial Owners, Directors and Management
(Page 88)
As of the record date, the directors and current executive
officers of Ligand beneficially owned in the
aggregate shares,
representing approximately % of the
shares of our common stock entitled to vote at the special
meeting.
Revocability
of Proxies (Page 12)
Any Ligand registered stockholder (meaning a stockholder that
holds stock in its own name) entitled to vote may submit a proxy
by telephone or the Internet or by returning the enclosed proxy
card by mail, or may vote in person by appearing at the special
meeting. If your shares are held in street name by
your broker, you should instruct your broker on how to vote your
shares using the instructions provided by your broker. If you do
not provide your broker with instructions, your shares will not
be voted and that will have the same effect as a vote against
the asset sale.
Any Ligand registered stockholder who executes and returns a
proxy card (or submits a proxy via telephone or the Internet)
may revoke the proxy at any time before it is voted in any one
of the following ways:
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delivering to the Secretary of Ligand a written instrument that
revokes the proxy;
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submitting another properly completed proxy with a later
date; or
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attending the special meeting and voting in person.
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Simply attending the special meeting will not constitute
revocation of a proxy. If you have instructed your broker to
vote your shares, the above-described options for revoking your
proxy do not apply and instead you must follow the directions
provided by your broker to change your instructions.
The Asset
Sale
The
Asset Sale (Page 14)
On September 6, 2006, our board of directors, at a meeting
duly called and held, approved the asset sale by and between
Ligand, King and King R&D, pursuant to an asset purchase
agreement, dated as of September 6, 2006, a copy of which
is included as Annex A to this proxy statement. Please read
it carefully. Ligand, King and King R&D may sometimes be
referred to in this proxy statement as a party, or collectively
as the parties. Pursuant to the terms of the asset purchase
agreement:
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we intend to sell all of our rights in and to
AVINZA®
(morphine sulfate extended-release capsules), in the United
States, its territories and Canada, which would constitute a
sale of all or substantially all of our assets under Delaware
law; and
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in exchange for our rights in and to
AVINZA®,
King and King R&D have agreed to pay us $265 million in
cash, subject to specific inventory adjustments, assume a
payment obligation of Ligand to Organon of approximately
$48 million (or reimburse Ligand at closing of the asset
sale to the extent any such amounts have been paid), assume the
Companys existing co-promote termination obligation to
make payments to
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Organon based on net sales of
AVINZA®,
and assume specified existing royalty obligations to other third
parties. The Company will also receive certain royalty payments
based on Kings annual net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017. At closing of the asset sale
$15 million of the cash payment will be funded into an
escrow to support any indemnification claims made by King within
the first year of closing.
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Reasons
for the Asset Sale (Page 21)
In evaluating the asset sale, our board of directors considered
the recommendations of the strategic alternatives committee, its
consultations with our management and financial and legal
advisors and various factors. For the material factors
considered by our board of directors in reaching its decision to
approve the asset sale and adopt the asset purchase agreement,
see The Asset Sale Reasons for the Asset
Sale, beginning on page 21.
Recommendation
of Our Board of Directors (Page 23)
After careful consideration, our board of directors has
unanimously:
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determined that the asset sale, the asset purchase agreement and
the transactions contemplated thereby are advisable and fair to
and in the best interests of Ligand and our stockholders;
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approved the asset sale and adopted the asset purchase
agreement; and
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recommended that Ligands stockholders vote FOR
the approval of the asset sale and adoption of the asset
purchase agreement.
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Opinion
of Our Financial Advisor (Page 23 and
Annex B)
In connection with the asset sale, Ligands board of
directors received a written opinion, dated September 6,
2006, from Ligands financial advisor, UBS Securities LLC,
or UBS, as to the fairness, from a financial point of view and
as of the date of such opinion, to Ligand of the aggregate
consideration to be received by Ligand in the asset sale. The
full text of UBS written opinion, dated September 6,
2006, is attached to this proxy statement as Annex B. We
encourage you to read this opinion carefully and in its entirety
for a description of the assumptions made, procedures followed,
matters considered and limitations on the review undertaken.
UBS opinion, which was provided to Ligands board
in connection with its evaluation of the aggregate consideration
from a financial point of view, does not address any other
aspect of the asset sale and does not constitute a
recommendation to any stockholder as to how to vote or act with
respect to the transaction.
Proceeds
from the Asset Sale (Page 27)
While we are evaluating a distribution of a substantial portion
of the net cash proceeds from the asset sale to our stockholders
in the form of a special dividend, we cannot predict the timing
or amount of such distribution, if any, to be made to our
stockholders. The amount, if any, available to our stockholders
will be determined by our board of directors, after weighing the
companys remaining liabilities and operational needs.
Effects
of the Asset Sale (Page 27)
If the asset sale is approved and the asset purchase agreement
is adopted by our stockholders and the other conditions to
closing of the asset sale are satisfied, we expect to become a
highly-specialized research and development and royalty company.
Other
Agreements and Transactions Related to the Asset Sale
(Page 29)
In addition to the asset purchase agreement, we also entered
into the following related agreements and transactions in
connection with the asset sale:
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a contract sales force agreement with King, pursuant to which
King agreed to conduct a detailing program to promote the sale
of
AVINZA®;
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a loan arrangement with King, pursuant to which King loaned to
us, $37.75 million; and
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as a condition to closing the asset sale, we are also required
to mail a notice of redemption to each of the holders of our 6%
Convertible Subordinated Notes, due 2007, which we mailed on
October 30, 2006.
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Other
Agreements and Transactions Related to our Strategic Review
Process (Page 29)
In connection with our overall strategic review process we also
entered into the following agreements:
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an asset purchase agreement with Eisai Inc. and Eisai Co., Ltd.,
pursuant to which we sold to Eisai Inc. and Eisai Co., Ltd. all
of our rights to our marketed oncology products; and
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a sale and leaseback transaction for our corporate headquarters
with Slough Estates USA Inc.
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Interests
of Ligands Directors and Executive Officers in the Asset
Sale (Page 29)
After the closing of the asset sale, King and King R&D have
agreed to indemnify and hold our executive officers and
directors harmless from any loss arising out of any breach of
representations and warranties by King, or a failure by King to
perform covenants applicable to them under the asset purchase
agreement. All of our directors and executive officers own
shares of our common stock
and/or
options to purchase shares of our common stock, and to that
extent, their interests in the asset sale are the same as that
of other holders of our common stock. See Security
Ownership of Certain Beneficial Owners, Directors and
Management, beginning on page 88.
Dissenters
Rights (Page 30)
You will not experience any change in your rights as a
stockholder as a result of the asset sale. None of Delaware law,
our certificate of incorporation or our bylaws provides for
appraisal or other similar rights for dissenting stockholders in
connection with the asset sale. Accordingly, you will have no
right to dissent and obtain payment for your shares.
Material
U.S. Federal and State Income Tax Consequences
(Page 30)
The asset sale will not result in any U.S. federal income
tax consequences to our stockholders. The transaction will be a
taxable event to Ligand for U.S. federal income tax
purposes, but Ligand anticipates that a substantial portion or
all of the taxable gain resulting from the asset sale will be
offset by net operating losses. For a complete description of
the material tax consequences of the asset sale to Ligand,
please see Material U.S. Federal and State Income Tax
Consequences, beginning on page 30.
Regulatory
Matters (Page 30)
On October 5, 2006, we were notified that we had been
granted early termination of the waiting period under the HSR
Act.
Asset
Purchase Agreement (Page 31)
No
Negotiation (Page 34)
The asset purchase agreement restricts our ability to solicit or
engage in discussions or negotiations with third parties
regarding specified transactions involving Ligand.
Notwithstanding these restrictions, under certain limited
circumstances, our board of directors may respond to an
alternative acquisition proposal, change its recommendation with
respect to the asset sale
and/or
terminate the asset purchase agreement and enter into an
alternative agreement if it constitutes a superior proposal
under the asset purchase agreement after paying the termination
fee specified in the asset purchase agreement.
Conditions
to Completion of the Asset Sale (Page 35)
Before we can complete the asset sale, a number of conditions
must be satisfied. These include, among other things:
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the absence of any governmental or court order that enjoins,
restrains, prohibits, or makes illegal the asset sale;
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the expiration or termination of the applicable waiting period
under the HSR Act, which condition was satisfied on
October 5, 2006, when we were notified that we had been
granted early termination of the waiting period under the HSR
Act;
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the receipt of our stockholder approval;
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the accuracy of the parties representations and
warranties, subject to specified materiality qualifications;
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the performance by each party of its obligations under the asset
purchase agreement in all material respects;
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the delivery of specified third-party consents;
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the execution and delivery of specified agreements; and
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the redemption or conversion of all outstanding Ligand 6%
Convertible Subordinated Notes due 2007.
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Other than the conditions pertaining to our stockholder approval
and the absence of governmental or court orders, either Ligand
on the one hand, or King on the other hand, may elect to waive
conditions to their respective performance and consummate the
asset sale.
4
Termination
(Page 36)
The asset purchase agreement may be terminated and the asset
sale may be abandoned at any time prior to consummation of the
asset sale by:
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the mutual written consent of both parties;
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either King or us, if the asset sale has not been completed by
December 31, 2006 and, in either case, the failure to
complete the asset sale by such date is not the result of the
failure of the party seeking to terminate the asset purchase
agreement of its obligations under the asset purchase agreement;
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either King or us, if our stockholders do not adopt the asset
purchase agreement at the special meeting;
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either King or us, if the other party is in material breach of
the asset purchase agreement, which breach is not cured within
10 days of the breaching party being notified of such
breach;
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us, if our board of directors has determined that an acquisition
proposal is a superior proposal;
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King, if, prior to the adoption of the asset purchase agreement
by our stockholders, our board of directors:
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fails to include in this proxy statement its recommendation of
the asset purchase agreement; or
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approves or recommends an acquisition proposal to our
stockholders or approves or recommends that our stockholders
tender their shares of common stock in any tender offer or
exchange offer that is an acquisition proposal;
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King, if it receives written notice from us that our board of
directors has determined that an acquisition proposal is a
superior proposal.
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Termination
Fee (Page 37)
We are obligated to pay King a termination fee of
$12 million if we or King terminates the asset purchase
agreement under certain circumstances.
5
QUESTIONS
AND ANSWERS ABOUT THE SPECIAL MEETING, PROPOSED ASSET SALE AND
THE PROPOSED AMENDMENT TO THE 2002 PLAN
The
Special Meeting
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Q: |
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Why am I receiving this proxy statement and proxy card? |
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You are receiving a proxy statement and proxy card because you
owned shares of our common stock as of the record date. This
proxy statement and proxy card relate to Ligands special
meeting of stockholders (and any adjournment thereof) and
describes the matters on which we would like you, as a
stockholder, to vote. |
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Where and when is the special meeting? |
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The special meeting will take place at the La Jolla
Marriott located at 4240 La Jolla Village Drive,
La Jolla, California 92037
on ,
2006 at 9:00 a.m., local time. |
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Who is soliciting my proxy? |
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Our board of directors is soliciting your proxy for use at the
special meeting. |
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What proposals will be voted on at the special meeting? |
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A: |
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You will be asked to consider and vote on the following
proposals: |
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to approve the sale of all or substantially all of our assets
under Delaware law through the sale of our rights in and to
AVINZA®
(morphine sulfate extended-release capsules), in the United
States, its territories and Canada, pursuant to the asset
purchase agreement attached as Annex A to this proxy
statement;
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to approve the amendment of our 2002 Plan, to allow equitable
adjustments to be made to options subject to the 2002 Plan in
the event of the payment of a large non-recurring cash dividend;
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to approve adjournment of the special meeting, if necessary, to
facilitate the approval of the foregoing, including to permit
the solicitation of additional proxies if there are not
sufficient votes at the time of the special meeting to establish
a quorum or to approve the foregoing; and
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to transact such other business as may properly be brought
before the special meeting or any adjournment or postponement
thereof.
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Why are we asking for a stockholder vote? |
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Delaware law requires that a Delaware corporation obtain
approval from its stockholders for the sale of all or
substantially all of its property and assets. Obtaining
stockholder approval is also a condition to closing of the asset
sale under the terms of the asset purchase agreement we
negotiated with King. In addition, Nasdaq rules require that
stockholder approval be obtained for any material amendment to
an equity compensation plan such as the 2002 Plan. |
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Who is entitled to vote? |
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Record holders of our outstanding shares of common stock as
of ,
2006 are entitled to vote. |
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How many votes do I have? |
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Each record holder of common stock is entitled to one vote per
share of common stock. |
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How many shares may vote at the special meeting? |
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As of the record date
of ,
2006, we had outstanding shares of common stock, which are all
eligible to vote at the special meeting. |
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How does our Board of Directors recommend that I vote? |
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The board of directors unanimously recommends that you vote: |
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FOR the proposal to approve the asset sale and adopt
the asset purchase agreement;
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FOR the proposal to approve the amendment to the
2002 Plan; and
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FOR the adjournment of the special meeting, if
necessary, to solicit additional proxies if there are not
sufficient votes at the time of the special meeting to establish
a quorum or to approve the asset sale.
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What vote of our stockholders is required to approve the
asset sale and adopt the asset purchase agreement? |
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For us to complete the asset sale, stockholders holding at least
a majority of the shares of our outstanding common stock at the
close of business on the record date must vote FOR
the resolution approving the asset sale and adopting the asset
purchase agreement. |
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What vote of our stockholders is required to approve the
amendment to the 2002 Plan? |
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For us to amend the 2002 Plan, stockholders holding at least a
majority of the shares of our outstanding common stock
represented in person or by proxy and entitled to vote at the
special meeting must vote FOR the proposal. |
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What vote of our stockholders is required to approve the
proposal to adjourn the special meeting, if necessary, to
solicit additional proxies? |
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The affirmative vote of a majority of the outstanding shares of
our common stock present or represented by proxy at the special
meeting and entitled to vote on the matter. |
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Q: |
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What is the share ownership of our directors and executive
officers? |
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As of the close of business on the record
date, ,
2006, our directors and executive officers collectively owned of
the outstanding shares of our common stock,
representing % of the shares
entitled to vote at the special meeting. For more information on
the share ownership of our directors and executive officers see
Security Ownership of Certain Beneficial Owners, Directors
and Management, beginning on page 87). |
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Am I entitled to appraisal or dissenters rights in
connection with the asset sale? |
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No. Holders of shares of our outstanding common stock will
not have appraisal or dissenters rights in connection with
either the asset sale or amendments to the 2002 Plan. |
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What do I need to do now? |
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After carefully reading and considering the information
contained in this proxy statement, please vote your shares by
completing, signing, dating and returning the enclosed proxy
card in the enclosed return envelope, by granting a proxy using
the telephone number printed on your proxy card; or by granting
a proxy using the Internet instructions printed on your proxy
card. You can also attend the special meeting and vote in
person. The special meeting will take place
on ,
2006. Our board of directors unanimously recommends that you
vote FOR of the asset sale and amendments to the
2002 Plan. |
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Can I change my vote after I have mailed in my signed proxy
card? |
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Yes. You can change your vote at any time before we vote your
proxy at the special meeting. You can do so in three ways.
First, you can send written notice stating that you would like
to revoke your proxy to our Secretary at the address given
below. Second, you can request a new proxy card and complete and
send it to our Secretary at the address given below. Third, you
can attend the special meeting and vote in person. You should
send any written notice or request for a new proxy card to the
attention of the Secretary, 10275 Science Center Drive,
San Diego, California 92121. |
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If my shares are held in street name by my
broker, will my broker vote my shares for me? |
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Your broker or other nominee will vote your shares only if you
provide instructions on how to vote to such broker or other
nominee. Following the directions provided by your broker or
other nominee, you should instruct your broker or other nominee
to vote your shares. Without your instructions, your shares will
not be voted, which will have the same effect as a vote against
the asset sale. |
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How will we solicit proxies? |
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A: |
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Proxies may be solicited in person, by telephone, facsimile,
mail or
e-mail by
our directors, officers and employees without additional
compensation. Brokers, nominees, fiduciaries, and other
custodians have been requested to forward soliciting material to
the beneficial owners of shares of our common stock held of
record by them, and we will reimburse such custodians for their
reasonable expenses. |
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Q: |
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Who can help answer further questions about the asset
sale? |
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A: |
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If you have more questions about the asset sale, the amendment
to the 2002 Plan, the special meeting or this proxy statement,
you should contact Ligands Secretary at 10275 Science
Center Drive, San Diego, California 92121. |
The
Asset Sale
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What is the proposed asset sale? |
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A: |
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The proposed asset sale is the sale of all of our rights in and
to
AVINZA®
(morphine sulfate extended-release capsules), in the United
States, its territories and Canada to King, and its wholly-owned
subsidiary King R&D, pursuant to an asset purchase
agreement, dated as of September 6, 2006. In exchange for
our rights, King and King R&D have agreed to pay us
$265 million in cash, subject to specific inventory
adjustments, and assume a payment obligation of Ligand to
Organon of approximately $48 million (or reimburse Ligand
at closing of the asset sale to the extent any such amounts have
been paid), assume the Companys existing co-promote
termination obligation to make payments to Organon based on net
sales of
AVINZA®
and assume specified existing royalty obligations to other third
parties. The Company will also receive certain royalty payments
based on Kings annual net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017. At closing of the asset sale
$15 million of the cash payment will be funded into an
escrow to support any indemnification claims made by King within
the first year of closing. The full text of the asset purchase
agreement is included as Annex A to this proxy statement. |
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Q: |
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Why is the Ligand board of directors recommending the
approval of the asset sale and adoption of the asset purchase
agreement? |
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A: |
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The board of directors has unanimously approved the asset sale
and adopted the purchase agreement. In evaluating the asset
sale, our board of directors considered the recommendations of
the strategic alternatives committee, its consultations with our
management and financial and legal advisors and various factors.
For the material factors considered by our board of directors in
reaching its decision to approve and adopt the asset purchase
agreement, see The Asset Sale Reasons for the
Asset Sale, beginning on page 21. |
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What do you expect to do with the proceeds from the asset
sale? |
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A: |
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While we are evaluating a distribution of a substantial portion
of the net cash proceeds from the asset sale to our stockholders
in the form of a special dividend, we cannot predict the timing
or amount of such distribution, if any, to be made to our
stockholders. The amount, if any, available to our stockholders
will be determined by our board of directors, after weighing the
companys remaining liabilities and operational needs. |
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Q: |
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When do you expect the asset sale to be completed? |
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A: |
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We are working to complete the asset sale as quickly as
practicable. If all necessary approvals have been obtained,
including stockholder and regulatory approvals, and any third
party consents, we hope to complete the asset sale shortly after
this special meeting scheduled
for ,
2006. |
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Q: |
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What will happen if the asset sale is approved? What will
happen if it is not approved? |
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A: |
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If the asset sale is approved, King and King R&D will
acquire all of our rights in and to
AVINZA®
in the United States, its territories and Canada. This will
constitute the sale of substantially all of our assets under
Delaware law. If approved, we expect to become a
highly-specialized research and development and royalty company
following the consummation of the asset sale. If the asset sale
is not approved by the holders of a majority of our outstanding
shares, then either we or King may terminate the asset purchase
agreement and our board of directors, along with management,
will reassess our options in light of our long-term strategic
goals. |
8
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Q: |
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Is the asset sale subject to conditions? |
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Yes. In addition to the approval of the asset sale and adoption
of the asset purchase agreement by our stockholders, the asset
sale is subject to satisfaction of various conditions,
including, among other things, the expiration or termination of
the applicable waiting periods under the HSR Act, and the
redemption or conversion of all outstanding Ligand 6%
Convertible Subordinated Notes due 2007. For a description of
these conditions, please see The Asset Purchase
Agreement Conditions to the Completion of the Asset
Sale, beginning on page 35. |
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Q: |
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Will the asset sale be a taxable transaction to me? |
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A: |
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The asset sale will not result in any U.S. federal income
tax consequences to our stockholders. The transaction will be a
taxable event to Ligand for U.S. federal income tax
purposes, but Ligand anticipates that a substantial portion or
all of the taxable gain resulting from the asset sale will be
offset by net operating losses. For a complete description of
the material tax consequences of the asset sale to Ligand,
please see Material U.S. Federal and State Income Tax
Consequences, beginning on page 30. |
The
2002 Plan
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Q: |
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Why is Ligand proposing to amend the 2002 Plan? |
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A: |
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Ligand is proposing the amendment to the 2002 Plan to enable it
to maintain the retention benefits derived from the outstanding
options held by our directors, officers and employees by
preserving the potential rewards of those options in the event
of a large cash dividend to our stockholders. |
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Q: |
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What will happen if the proposed amendment to the 2002 Plan
is approved? What will happen if it is not approved? |
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A: |
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If the proposed amendment is approved, Ligand will be able to
adjust the outstanding options to reflect any special cash
dividend that may be paid to our stockholders after the
consummation of the asset sale. Such adjustments may take the
form of either an adjustment to each outstanding options
strike price
and/or the
number of shares granted under such option in order to equitably
reflect the amount of cash distributed to our stockholders as a
cash dividend. As a result of the plan modification, any such
adjustments to the terms of outstanding options would be
considered a modification for accounting purposes and result in
the recognition of compensation expense in the Companys
consolidated statement of operations under the requirements of
Statement of Financial Accounting Standard No 123(R)
Share-Based Payment. Any such expense could be material.
If the proposed amendment to the 2002 Plan is not approved by
the holders of a majority of our outstanding shares present at
the meeting and we make a large cash dividend to our
stockholders, a large percentage of the outstanding options may
lose much, if not all, of their value and will no longer help us
retain the talent we believe we need to operate the company on
an ongoing basis. The amendments to the stock option plan have
been approved by our board of directors. |
9
CAUTIONARY
STATEMENT CONCERNING
FORWARD-LOOKING INFORMATION
This proxy statement, and the documents to which we refer you in
this proxy statement, contain forward-looking statements about
our plans, objectives, expectations and intentions.
Forward-looking statements include information concerning
possible or assumed future results of operations of Ligand, the
expected completion and timing of the asset sale and other
information relating to the asset sale. There are
forward-looking statements throughout this proxy statement,
including, among others, under the headings Summary,
Effects of the Asset Sale, and in statements
containing the words believes, expects,
estimates, forecasts, seeks,
may, will, and continues or
other similar words or expressions. You should read statements
that contain these words carefully. They discuss our future
expectations or state other forward-looking information, and may
involve known and unknown risks over which we have no control,
including, without limitation:
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the inability to complete the asset sale due to the failure to
satisfy the conditions to consummation of the asset sale,
including the failure to obtain stockholder approval;
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the occurrence of any event, change or other circumstances that
could give rise to the termination of the asset purchase
agreement;
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the failure of the asset sale to close for any other reason;
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the ability to recognize the benefits of the asset sale;
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the outcome of legal proceedings that may be instituted against
us and others in connection with the asset purchase agreement;
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the amount of the costs, fees, expenses and charges related to
the asset sale;
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the effect of the announcement of the asset sale on our client
relationships, operating results and business generally,
including the ability to retain key employees; and
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risks, uncertainties and factors set forth in our reports and
documents filed with the Securities and Exchange Commission, or
the SEC (which reports and documents should be read in
conjunction with this proxy statement).
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See Where You Can Find Additional Information on
page 92. You should not place undue reliance on
forward-looking statements. We cannot guarantee any future
results, levels of activity, performance or achievements. All
forward-looking statements contained or incorporated by
reference in the proxy statement speak only as of the date of
this proxy statement or as of such earlier date that those
statements were made and are based on current expectations or
expectations as of such earlier date and involve a number of
assumptions, risks and uncertainties that could cause the actual
result to differ materially from such forward-looking
statements. Except as required by law, we undertake no
obligation to update or publicly release any revisions to these
forward-looking statements or reflect events or circumstances
after the date of this proxy statement.
10
THE
SPECIAL MEETING
We are furnishing this proxy statement to you, as a stockholder
of Ligand, as part of the solicitation of proxies by our board
of directors for use at the special meeting of stockholders. In
this proxy statement, the terms Ligand,
company, we, our,
ours, and us refer to Ligand
Pharmaceuticals Incorporated, a Delaware corporation, and its
subsidiaries. The term asset purchase agreement
refers to the Purchase Agreement, dated as of September 6,
2006, by and between Ligand Pharmaceuticals Incorporated, King
Pharmaceuticals, Inc., and King Pharmaceuticals Research and
Development, Inc. The term asset sale refers to the
proposed sale of all of our rights in and to
AVINZA®
to King and King R&D pursuant to the asset purchase
agreement. The term King refers to King
Pharmaceuticals, Inc., and the term King R&D
refers to King Pharmaceuticals Research and Development, Inc.
Date,
Time, Place and Purpose of the Special Meeting
This proxy statement is being furnished to our stockholders in
connection with the solicitation of proxies by our board of
directors for use at that special meeting to be held at the
La Jolla Marriott located at 4240 La Jolla Village
Drive, La Jolla, California 92037
on ,
2006 at 9:00 a.m., local time. The purpose of the special
meeting is:
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to consider and to vote on a proposal to approve the asset sale,
which will constitute the sale of substantially all of the
assets of Ligand to King and King R&D and approve the asset
purchase agreement;
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to consider and to vote on a proposal to amend Ligands
2002 Stock Incentive Plan, referred to herein as the 2002 Plan,
to allow equitable adjustments to be made to options outstanding
under the 2002 Plan in the event of the payment of a large
non-recurring cash dividend;
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to approve adjournment of the special meeting, if necessary, to
permit the solicitation of additional proxies if there are not
sufficient votes at the time of the special meeting to establish
a quorum or to approve the asset sale and adopt the asset
purchase agreement; and
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to transact such other business as may properly be brought
before the special meeting or any adjournment or postponement
thereof.
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Our board of directors has unanimously determined that the
approval of the asset sale is advisable and that the asset sale
is fair and in the best interest of our stockholders.
Accordingly, our board of directors unanimously recommends that
our stockholders vote FOR the approval of the
asset sale.
In addition, our board of directors has approved the amendment
of the amendment of the 2002 Plan that would allow equitable
adjustments to be made to options outstanding under the 2002
Plan in the event a special cash dividend is paid to our
stockholders. Accordingly, our board of directors recommends
that our stockholders vote FOR the approval
of the amendment of the 2002 Plan.
Record
Date, Voting and Quorum
Our board of directors fixed the close of business
on ,
2006, as the record date for the determination of holders of our
outstanding shares entitled to notice of and to vote on all
matters presented at the special meeting. Such stockholders will
be entitled to one vote for each share held on each matter
submitted to a vote at the special meeting. As of the record
date, there
were shares
of our common stock, $0.001 par value per share, issued and
outstanding, each of which is entitled to one vote on each
matter to be voted upon. You may vote in person or by proxy.
The required quorum for the transaction of business at the
special meeting is a majority of the votes eligible to be cast
by holders of shares of our common stock issued and outstanding
on the record date. Shares that are voted FOR, or
AGAINST a proposal or marked ABSTAIN are
treated as being present at the special meeting for purposes of
establishing a quorum and are also treated as shares entitled to
vote at the special meeting with respect to such proposal.
Broker non-votes and the shares of common stock as
to which a stockholder abstains are included for purposes of
determining whether a quorum of shares of common stock is
present at a meeting. A broker non-vote occurs when
a nominee holding shares of common stock for the beneficial
owner does not vote on a
11
particular proposal because the nominee does not have
discretionary voting power with respect to that item and has not
received instructions from the beneficial owner.
Required
Vote
Approval of the asset sale requires the affirmative vote of the
holders of a majority of the outstanding shares of our common
stock entitled to vote at the special meeting. The proposals to
amend the 2002 Plan and to adjourn the meeting, if necessary, to
solicit additional proxies, each require the affirmative vote of
the holders of a majority of the outstanding shares of our
common stock present or represented by proxy at the special
meeting and entitled to vote on the matter.
Each holder of a share of our common stock is entitled to one
vote per share. Failure to vote by proxy (by returning a
properly executed proxy card or by following the instructions
printed on the proxy card for telephone and Internet voting) or
to vote in person will not count as votes cast or shares voting
on the proposals. Since the first proposal requires the approval
of the holders of a majority of our shares outstanding, both
broker non-votes and abstentions would have the same
effect as votes against such proposal. With respect to the
second, third and fourth proposals, to approve the adjournment
of the special meeting, if necessary, neither broker
non-votes nor abstentions are included in the
tabulation of the voting results and, therefore, they do not
have the effect of votes against such proposals.
Voting
Stockholders may vote their shares:
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by attending the special meeting and voting their shares of our
common stock in person;
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by completing the enclosed proxy card, signing and dating it and
mailing it in the enclosed post-prepaid envelope;
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by using the telephone number printed on your proxy card; or
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by using the Internet by going to
http://www.proxyvoting.com/lgnd and following the instructions
printed on your proxy card.
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Our board of directors is asking for your proxy. Giving the
board of directors your proxy means you authorize it to vote
your shares at the special meeting in the manner you direct. You
may vote for or against the proposals or abstain from voting.
All valid proxies received prior to the special meeting will be
voted. All shares represented by a proxy will be voted, and
where a stockholder specifies by means of the proxy a choice
with respect to any matter to be acted upon, the shares will be
voted in accordance with the specification so made. If no choice
is indicated on the proxy, the shares will be voted
FOR the approval of the asset sale and adoption of
the asset purchase agreement, the amendment to the 2002 Plan and
as the proxy holders may determine in their discretion with
respect to any other matters that properly come before the
special meeting.
Stockholders who have questions or requests for assistance in
completing or submitting proxy cards should contact us at
1-800-356-2017.
Stockholders who have their shares in street name,
meaning the name of a broker or other nominee who is the record
holder, must either direct the record holder of their shares to
vote their shares or obtain a proxy from the record holder to
vote their shares at the special meeting.
Revocability
of Proxies
A stockholder giving a proxy has the power to revoke his or her
proxy, at any time prior to the time it is voted, by:
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delivering to the Secretary of Ligand a written instrument that
revokes the proxy;
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submitting another properly completed proxy with a later
date; or
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attending the special meeting and voting in person.
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Simply attending the special meeting will not constitute
revocation of your proxy. If your shares are held in the name of
a broker or other nominee who is the record holder, you must
follow the instruction of your broker or other nominee to revoke
a previously given proxy.
The form of proxy accompanying this proxy statement confers
discretionary authority upon the named proxyholders with respect
to amendments or variations to the matters identified in the
accompanying Notice of Special Meeting and with respect to any
other matters which may properly come before the special
meeting. As of the date of this proxy statement, management
knows of no such amendment or variation or of any matters
expected to come before the special meeting which are not
referred to in the accompanying Notice of Special Meeting.
Attendance
at the Special Meeting
Only holders of common stock, their proxy holders and guests we
may invite may attend the special meeting. If you wish to attend
the special meeting in person but you hold your shares through
someone else, such as a stockbroker, you must bring proof of
your ownership and identification with a photo at the special
meeting. For example, you could bring an account statement
showing that you beneficially owned shares of common stock of
Ligand as of the record date as acceptable proof of ownership.
Solicitation
of Proxies
In addition to solicitation by mail, our directors, officers and
employees may solicit proxies by telephone, other electronic
means or in person. These people will not receive compensation
for their services, but we will reimburse them for their
out-of-pocket
expenses. We will bear the cost of printing and mailing proxy
materials, including the reasonable expenses of brokerage firms
and others for forwarding the proxy materials to beneficial
owners of common stock.
Other
Business
We are not currently aware of any business to be acted upon at
the special meeting other than the matters discussed in this
proxy statement. Under our bylaws, business transacted at the
special meeting is limited to the purposes stated in the notice
of special meeting, which is provided at the beginning of this
proxy statement. If other matters do properly come before the
special meeting, or at any adjournment or postponement of the
special meeting, we intend that shares of our common stock
represented by properly submitted proxies will be voted in
accordance with the recommendations of our board of directors.
13
PROPOSAL ONE:
THE ASSET SALE
The following is a description of the material aspects of the
asset sale, including background information relating to the
proposed terms of the asset purchase agreement. While we believe
that the following description covers the material terms of the
asset sale, the asset purchase agreement and other arrangements
between King and King R&D and us, the description may not
contain all of the information that is important to you. In
particular, the following summary of the asset purchase
agreement is not complete and is qualified in its entirety by
reference to the copy of the asset purchase agreement attached
to this proxy statement as Annex A and incorporated by
reference herein. You should carefully read this proxy statement
and the other documents to which we refer, including the asset
purchase agreement, for a complete understanding of the terms of
the asset sale.
Background
of the Asset Sale
Ligands board of directors and management have from time
to time evaluated and considered a variety of strategic
alternatives as part of our long-term strategy to maximize
stockholder value.
In September 2005, as we neared the end of our financial
restatement process (in 2005 we restated our consolidated
financial statements for the years 2002 and 2003, the quarters
of 2003, and the first three quarters of 2004, to correct errors
related to revenue recognition and other matters), we considered
retaining an investment banker to help us in evaluating
strategic alternatives, including the sale of the company as a
whole. UBS Securities LLC, or UBS, was subsequently engaged as
our financial advisor to assist us in our review of near-term
and long-term business and financial objectives and financial
and strategic alternatives. In addition, in late September 2005,
one of our largest shareholders began urging our board of
directors and management to take a number of actions, including
the evaluation of strategic options.
On October 31, 2005, our board of directors held a special
meeting, at which management presented to and discussed with our
board of directors, its proposed business plan and various
business and strategic alternatives. Our board of directors also
met with our financial advisor to discuss possible business and
strategic alternatives as part of our effort to maximize
stockholder value.
On November 18, 2005, we announced that we would be
exploring strategic alternatives to enhance shareholder value
and that we had engaged UBS as our financial advisor to assist
our board of directors and management in this process.
At regularly scheduled meetings held on
December 8th and
9th of
2005, our board of directors met and discussed Ligands
strategic review process with management and our financial and
legal advisors. Management presented to and discussed with our
board of directors its current strategic plan, including
financial projections and product trends, and other strategic
alternatives. Our board of directors also discussed with our
financial advisor the process proposed for evaluating possible
strategic alternatives, including the sale of the entire
company, the sale or divesture of our separate assets, including
our rights in
AVINZA®,
which we refer to herein as the
AVINZA®
assets, the establishment of a royalty trust, and a combination
of a sale of the company as a whole or selected commercial
assets with the establishment of a royalty trust. In addition, a
representative of our outside legal advisor, Latham &
Watkins LLP, discussed with our board of directors its fiduciary
duties under Delaware law in connection with this process. After
extended discussion, our board of directors directed management
and our financial advisor to conduct further work to evaluate
the strategic alternatives that had been discussed at the
meeting and to contact third parties regarding their interest in
pursuing a possible transaction with us.
Between December 2005 and February 2006, in accordance with our
board of directors directives, our financial advisor
contacted 78 interested parties, including 64 strategic parties
and 14 financial parties, regarding their interest in pursuing a
possible transaction with us. Confidentiality agreements were
executed with 38 interested parties, 24 other strategic parties
and 13 financial parties, each of which were provided with a
confidential information memorandum regarding Ligand. During
this period an electronic and a physical data room were
assembled that contained, among other things, financial, legal
and operational due diligence materials related to Ligand and
the
AVINZA®
assets.
14
On December 28, 2005, we executed a confidentiality
agreement with King and a copy of the confidential information
memorandum regarding Ligand was provided.
On January 17, 2006, we entered into a termination and
return of rights agreement with Organon USA, Inc., or Organon,
that terminated the
AVINZA®
co-promotion agreement between Ligand and Organon. Pursuant to
the termination and return of rights agreement Organon agreed to
continue to
promote AVINZA®
through September 30, 2006. The termination and return of
rights agreement also obligates Ligand to pay Organon an
approximately $48 million termination payment, with
approximately $38 million due on or before October 15,
2006, and an additional $10 million due on or before
January 15, 2007. Under certain circumstances, including
the sale of the
AVINZA®
assets, these cash payments will accelerate.
On or about January 19, 2006, at our board of
directors direction, our financial advisor contacted
representatives of King and the other interested parties to
inform them that Ligand had established February 10, 2006,
as the deadline for submission by interested parties of
preliminary, non-binding indications of interest with respect to
an acquisition of Ligand as a whole or the acquisition of one or
more of our assets, including the
AVINZA®
assets.
On or about February 10, 2006, we received preliminary,
non-binding indications of interest from King, and two other
strategic parties referred to herein as Company A and Company B,
for an acquisition of either the company as a whole or an
acquisition of the
AVINZA®
assets.
On February 16, 2006, our board of directors held a special
meeting, together with management and our financial and legal
advisors, to review and discuss the indications of interest
received to date. At the meeting, our financial advisor updated
our board of directors regarding the overall strategic review
process and reviewed with our board of directors the terms of
the indications of interest that had been received and certain
publicly available information relating to each of the companies
that had submitted bids. Following a discussion of the bids
received, our board of directors authorized management and our
financial advisor to continue discussions with the parties that
had submitted indications of interest, including inviting these
companies to conduct comprehensive due diligence and participate
in management presentations. Our board of directors also
instructed management and our financial advisor to continue to
evaluate our transaction options, including those discussed at
the board meetings held on December 8th and
9th of 2005, and invite other companies into the process.
From February 16 to mid-April 2006, our management made
presentations to three interested parties, including King on
March 6, 2006. The management presentations included a
general overview of our business, including the
AVINZA®
assets and our historical and projected financial performance.
In addition, during this time, our representatives conducted due
diligence calls with representatives of interested parties and
responded to requests for additional due diligence materials.
During the week of February 20, 2006, Company A and Company
B indicated that they would not be submitting a second round of
non-binding indications of interest.
During the week of March 6, 2006, in accordance with our
board of directors directives, our financial advisor
contacted an additional financial party, referred to herein as
Company C. On March 16, 2006, we executed a confidentiality
agreement with Company C, which submitted a preliminary
non-binding indication of interest on April 7, 2006.
On or about April 6, 2006, at our board of directors
direction, our financial advisor informed the interested parties
that Ligand had established April 24, 2006 as the deadline
for submission by interested parties of a second round of
non-binding indications of interest with respect to an
acquisition of the
AVINZA®
assets.
On April 11, 2006, King and Company C were provided a draft
asset purchase agreement for their review and comment.
On April 24, 2006, we received a second round non-binding
indication of interest from King for an acquisition of the
AVINZA®
assets, along with a
mark-up of
the draft asset purchase agreement previously provided by
Ligand. Company C declined to submit a second indication of
interest, citing issues with its financing.
On April 28, 2006, our board of directors held a special
meeting, together with management and our financial and legal
advisors, to review and discuss the strategic review process,
including Kings indication of interest. At the
15
meeting, our financial advisor updated our board of directors
regarding the overall strategic review process and reviewed with
our board the financial terms of Kings indication of
interest, which reflected a significant decrease in the purchase
price from the price reflected in Kings initial indication
of interest. Our board was informed by our financial advisor
that King had indicated that this reduction in Kings
proposed purchase price was a result of the due diligence King
had conducted to date. In addition, our legal advisors reviewed
with our board of directors the principal legal matters
reflected in the
mark-up of
the draft asset purchase agreement submitted by King. Management
provided our board of directors with an update on general
business matters, including our preliminary financial results
for the first quarter of 2006, and discussed with the board
financial reporting requirements for 2006. After extended
discussion, our board of directors directed management and our
financial advisor to continue to evaluate Ligands
strategic alternatives, including pursuing a potential
transaction with King.
During May 2006, representatives of King conducted additional
due diligence.
On May 25, 2006, our board of directors held a regular
meeting, together with management and our financial advisor, at
which our financial advisor updated our board with respect to
the strategic review process, including efforts to provide King
with the additional due diligence materials. Also at the
meeting, management and our financial advisor discussed with our
board of directors the other strategic alternatives, initially
discussed at the board meetings held on
December 8th and
9th of
2005.
On June 6, 2006, King submitted a revised indication of
interest which contained a proposed purchase price for the
acquisition of the
AVINZA®
assets significantly lower than the purchase price set forth in
its April 24, 2006 indication of interest.
On June 8, 2006, our board of directors held a special
meeting, together with management and our financial and legal
advisors, at which management and our financial advisor reviewed
with our board of directors Kings June 6, 2006
indication of interest. After extended conversation, our board
of directors decided to suspend negotiations with King at that
time. Following this determination, management led a discussion
of the status of the strategic review process in general and its
proposed business plan.
During June 2006, at our board of directors direction, our
financial advisor contacted parties which previously had
expressed an interest in the
AVINZA®
assets but had declined to submit either a preliminary or second
round indication of interest, including Company A and Company B,
and an additional four potential parties which had not been
contacted previously.
On June 13, 2006, our board of directors held a special
meeting at which the board of directors and management discussed
the formation of a strategic alternatives committee of our board
of directors to oversee the strategic review process. A
representative of our outside legal advisor, Latham &
Watkins LLP, also discussed with our board of directors its
fiduciary duties under Delaware law with respect to the
formation of a strategic alternatives committee to oversee the
strategic review process. Following a discussion of these
matters and the responsibilities to be delegated to the
strategic alternatives committee, our board of directors
established the strategic alternatives committee, comprised of
independent directors of our board of directors John Groom and
Michael A. Rocca and board member Brigette Roberts, to assist
our board of directors and management with its review and
supervision of the strategic review process and any resulting
transactions.
On June 15, 2006, the strategic alternatives committee held
a regular meeting, together with management and our financial
advisor, to review and discuss the strategic review process. At
the meeting, our financial advisor updated the committee
regarding the overall strategic review process, including
efforts to divest the
AVINZA®
assets. In addition, management presented and discussed with the
committee several contingency options should Ligand be unable to
divest the
AVINZA®
assets prior to the Organon termination date. These topics were
also discussed on June 21, 2006, our board of directors
held a regular meeting also attended by management and our
financial advisor.
Between early and mid-July 2006, our management made
presentations similar to those previously provided to the other
interested parties to each of Company A and Company B. During
this time, our representatives also conducted diligence calls
with representatives of each of Company A and Company B and
responded to requests for additional due diligence materials. In
addition, on July 13, 2006 Company A and Company B were
provided with a draft asset purchase agreement for their review
and comment.
16
On or about July 13, 2006, at the strategic alternative
committees direction, our financial advisor informed
Company A and Company B that Ligand had established
July 31, 2006 as the deadline for submission by interested
parties of a second round of non-binding indications of interest
with respect to an acquisition of the
AVINZA®
assets.
On or about July 25, 2006, Jason Aryeh, the general partner
of JALAA Equities, LP, one of our stockholders, had a telephonic
conversation with Adriann W. Sax, Executive Vice President,
Business Development and Strategic Planning of King, during
which Ms. Sax indicated that King was still interested in a
possible transaction with Ligand for the
AVINZA®
assets. Dating back to early 2005, Mr. Aryeh had been
independently contacting potential purchasers of Ligand to gauge
their interest in purchasing either Ligand as a whole or its
individual assets. It was in this context that Mr. Aryeh
began to develop a relationship with representatives of King,
including Ms. Sax and Neil Morton, Associate Director of
Business Development and Strategic Planning of King. From their
first telephone conversation on November 18, 2005,
Mr. Aryeh, Ms. Sax and Mr. Morton spoke on a
regular basis regarding a possible transaction with Ligand for
the
AVINZA®
assets. In addition, Mr. Aryeh provided King with diligence
materials that he had independently developed to aid King in its
due diligence process.
On July 26, 2006, our board of directors held a special
meeting at which management updated our board of directors
regarding the overall strategic review process and presented and
discussed with our board of directors managements current
operational initiatives to support Ligands ongoing
business. Following managements presentation, the
non-management members of the board of directors discussed the
strategic review process in an executive session.
On July 27, 2006, our board of directors reconvened at a
regular meeting, together with management and our financial
advisor. Following a discussion with management and our
financial advisor regarding the strategic review process, the
non-management members of our board of directors met in
executive session. Following this executive session David E.
Robinson, a director and our President, Chief Executive Officer
and Chairman of the Board, offered his resignation from his
positions as director, President, Chief Executive Officer, and
Chairman of the Board, to be effective as of July 31, 2006.
On July 28, 2006, Mr. Aryeh contacted Dr. Roberts
and Jeffrey R. Perry, one of our directors, regarding his
conversations with King and relayed Ms. Saxs
statement that King remained interested in a possible
transaction with Ligand for the
AVINZA®
assets.
On or about July 29, 2006, Dr. Roberts had
conversations with her fellow strategic alternative committee
members, Messrs. Groom and Rocca, regarding
Mr. Aryehs discussion with Ms. Sax.
On July 31, 2006, our board of directors held a special
meeting at which Henry F. Blissenbach, one of our directors, was
appointed as Chairman of the Board and Interim Chief Executive
Officer. Mr. Groom updated the board of directors regarding
the overall strategic review process and summarized for the
board Kings expression of interest in reengaging in the
process. In addition, our board of directors discussed the
possibility of utilizing Mr. Aryeh to help facilitate a
possible transaction with King regarding the sale of the
AVINZA®
assets. Following an extended discussion, our board of directors
authorized the strategic alternatives committee to ask
Mr. Aryeh to help facilitate a possible transaction with
King regarding the sale of the
AVINZA®
assets. On August 1, 2006, Mr. Aryeh entered into a
confidentiality agreement with Ligand.
On July 31 and August 1, 2006, we received a second
round non-binding indication of interest from Company A and
Company B, respectively. In addition, Company A provided Ligand
and our outside counsel with a
mark-up of
the draft asset purchase agreement. Pursuant to its written
proposal, Company A proposed to purchase the
AVINZA®
assets for a purchase price of $325 million in cash, but
did not offer to assume Ligands payment obligations under
the Organon termination and return of rights agreement. Pursuant
to its written proposal, Company B proposed to purchase the
AVINZA®
assets for a purchase price of $300 million in cash and
assume Ligands payment obligations of approximately
$48 million under the Organon termination and return of
rights agreement.
On August 1, 2006, Dr. Roberts and Mr. Aryeh met
with Brian A. Markison, President and Chief Executive Officer of
King, Ms. Sax, Steve Andrzejewski, Chief Commercial Officer
of King, and Mr. Morton at Kings offices in
Bridgewater, New Jersey, to discuss a possible transaction with
Ligand regarding the
AVINZA®
assets. At this
17
meeting the parties discussed financial terms of Kings bid
for the
AVINZA®
assets and process matters such as the status of Kings due
diligence.
On August 2, 2006, the strategic alternatives committee
held a meeting, together with management and our financial and
legal advisors, to review and discuss Company As and
Company Bs respective indications of interest. At the
meeting, our financial advisor updated the committee regarding
the overall strategic review process and reviewed with the
committee the terms of Company As and Company Bs
indications of interest, respectively, and certain publicly
available information relating to each of the companies. The
committee was informed by our financial advisor that each of
Company A and Company B had indicated that its proposed
acquisition was not fully funded, but that it was either working
with a current financing source or its existing equity sponsors
to develop a fully financed bid. Following an extensive
discussion of the bids received, the committee authorized
management and our financial advisor to continue discussions
with Company A and Company B, including inviting these companies
to conduct comprehensive due diligence and participate in
management presentations.
On August 4, 2006, the strategic alternatives committee
held a meeting with management and our financial and legal
advisors, to review and discuss the strategic review process. At
the meeting the committee was updated regarding the status of
discussions with Company A and Company B. The committee was also
updated with respect to the status of discussions with King,
including Kings request for an onsite due diligence visit
and concerns raised by King regarding Ligands current
inventory levels. After a discussion, the committee directed
management and Messrs. Perry and Aryeh to arrange a due
diligence visit at Ligands offices in San Diego,
California for August 7 through August 9, 2006.
From August 7 through August 9, 2006, representatives of
King, including Ms. Sax, Mr. Morton and
representatives of Kings financial advisor, Citigroup
Global Markets Inc., met with representatives of Ligand,
including Dr. Roberts, Mr. Aryeh, Andres
Negro-Vilar, M.D., Ph.D., Executive Vice President,
Research and Development, and Chief Scientific Officer of
Ligand, James LItalien, Ph.D., Senior Vice President,
Regulatory Affairs and Compliance of Ligand, and Tod G. Mertes,
CPA, Vice President, Controller and Treasurer of Ligand, at
Ligands offices in San Diego, California to discuss
Kings open diligence issues.
On August 10, 2006, the strategic alternatives committee
held a meeting, together with management and our financial and
legal advisors, to receive an update on the status of
discussions with Company A, Company B and King. The committee
was updated regarding the discussions with Company A and Company
B, and with respect to the status of discussions with King,
including Kings recent diligence visit to Ligands
offices and ongoing concerns raised by King regarding
Ligands current inventory levels. Mr. Aryeh discussed
with the committee several potential solutions to resolve these
concerns as well as fill the promotion gap to be vacated by
Organon beginning on October 1, 2006. After a discussion,
the committee authorized management and Mr. Aryeh to
continue discussions with King and to propose the potential
solutions discussed with the committee, including a possible
contract sales agreement with King, pursuant to which
Kings sales force would promote the
AVINZA®
product between October 1, 2006 and the closing of the
proposed sale of the
AVINZA®
assets.
On August 14, 2006, representatives of Ligand and Company A
telephonically discussed Company As
mark-up of
the draft asset purchase agreement. At the culmination of the
telephonic discussion, and at the strategic alternative
committees direction, Company A was informed that Ligand
had established August 24, 2006 as the deadline for
submission by interested parties of a final best offer and asked
that Company A submit a revised
mark-up of
the asset purchase agreement with its bid. Following these
discussions and in accordance with the strategic alternative
committees directives, our financial advisor also informed
Company B that Ligand had established August 24, 2006 as
the deadline for submission by interested parties of a final
best offer and asked that Company B submit a
mark-up of
the draft asset purchase agreement with its bid.
On August 15, 2006, we received a written indication of
interest from King pursuant to which King proposed to purchase
the
AVINZA®
assets for a purchase price of $250 million in cash, assume
Ligands payment obligations of approximately
$48 million under the Organon termination and return of
rights agreement, and pay a royalty based on Kings annual
net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017.
On August 15, 2006, the strategic alternatives committee
held a meeting with management and our financial and legal
advisors, to receive an update on the discussions with the
interested parties.
18
On August 15, 2006, King provided Ligand and our legal
advisor with a draft non-binding term sheet for an asset
purchase agreement to be entered into in connection with the
sale of the
AVINZA®
assets and a draft non-binding term sheet for a contract sales
force agreement. During the period from August 15, 2006
through August 22, 2006, representatives of Ligand and King
negotiated the terms of the two term sheets during several
telephonic meetings. In connection with these negotiations, on
August 18, 2006, Mr. Aryeh, Mr. Perry and a
representative of our outside legal counsel had a telephonic
meeting with Joseph Squicciarino, Chief Financial Officer of
King, Ms. Sax, James W. Elrod, General Counsel of King to
negotiate the terms of non-binding term sheets for the asset
purchase agreement and the contract sales force agreement. On
August 22, 2006, Dr. Blissenbach, Mr. Perry,
Mr. Aryeh and a representative of our outside legal counsel
met with Mr. Markison, Mr. Squicciarino, Ms. Sax,
Mr. Andrzejewski and Mr. Elrod, at Ligands
offices in San Diego, California, to finalize the terms of
the non-binding term sheets, including the structure of the
royalty payment. Pursuant to the non-binding term sheet, King
agreed to pay Ligand a 15% royalty during the first
20 months after the closing of the asset sale on its net
sales of the
AVINZA®
product. With respect to subsequent royalty payments King agreed
to pay Ligand a 5% royalty if its net sales were less than
$200 million, and if Kings calendar year net sales
were greater than $200 million, then the royalty payment
would be 10% of all of Kings net sales less than
$250 million, plus 15% of all of Kings net sales
greater than $250 million.
On August 21, 2006, our board of directors held a special
meeting at which management updated our board of directors
regarding the status of discussions with the three remaining
interested parties.
On August 23, 2006, King provided Ligand and our legal
advisors a draft contract sales force agreement.
On August 24, 2006, Company A submitted a final best offer
pursuant to which Company A increased its offer price from
$325 million to $350 million in cash and added 1%
royalty on Company As net sales for a period of five
years. Company B informed our financial advisor that it would
not be submitting a final best offer at that time, although it
remained interested in a possible transaction with Ligand.
On August 25, 2006, the strategic alternatives committee
held a special meeting with management and our financial and
legal advisors, to review and discuss Kings and Company
As respective bids. Our financial advisor reviewed with
the committee the terms of Company As bid and informed the
committee that Company B had indicated that it would not be
submitting a final best offer at that time, although it remained
interested in a possible transaction with Ligand. Our legal
advisor reviewed the principal legal aspects of Company As
mark-up of
the draft asset purchase agreement. The committee was also
updated with respect to the status of discussions with King and
discussed with Messrs. Perry and Aryeh the financial terms
of the non-binding term sheets for an asset purchase agreement
to be entered into in connection with the sale of the
AVINZA®
assets and the contract sales force agreement. Our legal advisor
reviewed the principal legal aspects of the terms sheets agreed
upon with King. After an extended discussion, the committee
directed management and our financial and legal advisors to
continue discussions with both King and Company A with respect
to a possible sale of the
AVINZA®
assets.
On August 25, 2006, King provided Ligand and our legal
advisors with a
mark-up of
the draft asset purchase agreement. Thereafter, management,
Mr. Aryeh and our outside legal advisor negotiated the
terms of the asset purchase agreement and contract sales force
agreement with Kings representatives.
On August 30, 2006 and August 31, 2006,
representatives of Company A discussed with our financial
advisor the value of Company As bid and pending due
diligence requirements, which Company A estimated would require
approximately two weeks to complete. Company A was informed that
a two week due diligence period could place Company A at a
substantial timing disadvantage. As a result of these
discussions, Company A increased the cash component of its offer
price from $350 million to $385 million and
restructured its proposed royalty payment to provide for a 1%
royalty for sales up to $100 million, which would increase
incrementally for each additional $100 million in sales up
to $500 million at which point the royalty would remain at
11%, as well as its duration.
On August 31, 2006, the strategic alternatives committee
held a meeting, together with management and our financial and
legal advisors, to review and discuss the status of negotiations
with King and Company A. At the meeting, our financial advisor
discussed with the committee financial aspects of Kings
and Company As proposals to purchase the
AVINZA®
assets. Our legal advisors also summarized and discussed with
the committee the material terms of the proposed asset purchase
agreements. After an extended discussion, the committee directed
19
management and our financial and legal advisors to continue
discussions with both King and Company A with respect to a
possible sale of the
AVINZA®
assets and inform them that Ligand had established
September 5, 2006 as the deadline for submission of final
best offers coupled with a fully negotiated asset purchase
agreement.
Following the strategic alternatives committee meeting, our
financial advisor informed Company A, in accordance with the
committees directives, of the September 5, 2006
deadline for submission of final best offers and discussed with
Company A its remaining diligence requirements. Company A
expressed an interest in completing its remaining due diligence
on an accelerated basis and negotiating the asset purchase
agreement. Over the next several days, management and our
advisors worked with Company A and its advisors to address its
due diligence requests and negotiate the asset purchase
agreement. Following the strategic alternatives committee
meeting, Mr. Aryeh informed King, in accordance with the
committees directives, of the deadline for submission of a
final best offer and a fully negotiated asset purchase
agreement. Over the next several days, Messrs. Perry and
Aryeh and our legal advisor worked with King to negotiate and
finalize the asset purchase agreement and contract sales force
agreement.
On September 4, 2006, Mr. Aryeh and Kings
financial advisor had a telephonic conversation to discuss
possible changes to Kings proposal. During this
discussion, Mr. Aryeh suggested that King offer to loan
Ligand, at Ligands option, an amount equal to the initial
termination payment Ligand will be required to make under the
termination and return of rights agreement with Organon, at a
favorable interest to Ligand, but which would be forgiven at
closing of the proposed asset sale, if the parties closed the
transaction prior to January 1, 2007. Later that day,
Mr. Perry had a telephonic conversation with Kings
financial advisor during which he urged King to raise the cash
component of its bid.
On September 5, 2006, Dr. Blissenbach and
Mr. Markison had a telephonic discussion to clarify
Kings proposal. As a result of these discussions, King
increased the cash component of its offer price from
$250 million to $265 million and offered to loan
Ligand, at Ligands option, up to $37.75 million at an
interest rate of 9.50%, which accrued interest amounts, if any,
would be forgiven at closing of the proposed asset sale, if the
parties closed the transaction prior to January 1, 2007.
Mr. Markison stated that this was Kings best and
final offer.
On September 5, 2006, the strategic alternatives committee
held a meeting, together with management and our financial and
legal advisors to review and discuss Kings and Company
As final best offers and asset purchase agreements,
respectively. Mr. Aryeh reviewed and discussed with the
committee the financial terms of Kings final best offer,
including the increase of upfront cash and the no-interest loan.
Our legal advisors reviewed and discussed with the committee its
fiduciary obligations under Delaware law in connection with the
proposed asset sale. Our legal advisors also summarized and
discussed with the committee the material terms of the asset
purchase agreements, including provisions permitting the board
of directors to change its recommendation to stockholders or
terminate the asset purchase agreement to accept a superior
proposal, subject to payment of a termination fee equal to
approximately 2.5% of the aggregate purchase price plus
reimbursement of Kings
out-of-pocket
expenses. Our financial advisor then reviewed with the committee
the events leading up to the asset sale. The committee, with the
assistance of management and our financial advisor, compared
financial terms of Kings and Company As final best
offers, including the different royalty payment structures,
managements view of the respective abilities of each
bidder to market
AVINZA®
going forward, the impact such abilities could have on the
relative attractiveness of the offers and the implications of
our existing net operating losses on the potential after-tax
value to be received by Ligand in the proposed transactions.
After an extended discussion regarding Kings proposal
relative to Company As, the committee concluded to
recommend that our board of directors approve the asset purchase
agreement to be entered into with King and recommend that our
stockholders approve the sale of the
AVINZA®
assets to King, based on the expected relative values of the
offers, the implications of our existing net operating losses on
the potential after-tax value to be received by Ligand in the
proposed transactions and the increased assurance of closing a
transaction with King.
On September 6, 2006, our board of directors held a special
meeting with management and our financial and legal advisors to
review and discuss Kings and Company As final best
offers and asset purchase agreements, respectively, and consider
the recommendation of the strategic alternatives committee to
approve the sale of the
AVINZA®
assets to King. Dr. Blissenbach reviewed and discussed with
the board the financial terms of the asset purchase agreement
with King and the events leading up to the asset sale. The board
discussed, with the assistance
20
of management and our financial advisor, financial terms of
Kings and Company As final best offers, including
the different royalty payment structures, managements view
of the respective abilities of each bidder to market
AVINZA®
going forward, the impact such abilities could have on the
relative attractiveness of the offers and the implications of
our existing net operating losses on the potential after-tax
value to be received by Ligand in the proposed transactions.
Mr. Groom discussed with our board of directors the
strategic alternatives committees process and relayed the
committees recommendation that the board of directors
approve the asset purchase agreement to be entered into with
King and recommend that our stockholders approve the sale of the
AVINZA®
assets to King. UBS then reviewed with our board of directors
its financial analysis of the aggregate consideration to be paid
by King for the
AVINZA®
assets, and delivered to our board of directors an oral opinion,
which opinion was confirmed by delivery of a written opinion
dated September 6, 2006, to the effect that, as of that
date and based on and subject to various assumptions, matters
considered and limitations described in its opinion, the
aggregate consideration to be received by Ligand in the
transaction was fair, from a financial point of view, to Ligand.
Our legal advisors reviewed and discussed with our board of
directors its fiduciary obligations under Delaware law in
connection with the asset sale. Our legal advisors also
summarized and discussed with our board the material terms of
the asset purchase agreement with King, including provisions
permitting the board of directors to change its recommendation
to stockholders or terminate the asset purchase agreement to
accept a superior proposal, subject to payment of a termination
fee equal to approximately 2.5% of the aggregate purchase price
plus reimbursement of Kings
out-of-pocket
expenses. After an extended discussion regarding the financial
and legal advantages of Kings proposal relative to Company
As proposal, our board unanimously approved the sale of
the
AVINZA®
assets to King and resolved to recommend that our stockholders
approve the sale of the
AVINZA®
assets to King.
The parties executed the asset purchase agreement and contract
sales agreement on September 6, 2006. On September 7,
2006, Ligand and King issued a press release announcing the
transaction.
Reasons
for the Asset Sale
In evaluating the asset sale, the board of directors considered
the recommendations of the strategic alternatives committee,
consulted with our management and financial and legal advisors,
reviewed a significant amount of information and considered a
number of factors. The material factors considered by the board
of directors were:
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the value and the consideration to be received by the company
pursuant to the asset purchase agreement, including the fact
that the company would receive an up-front cash payment, and
King would agree to assume certain payment obligations of
Ligand, plus Ligand would receive a certain royalty payment
based on Kings annual net sales of
AVINZA®
through
AVINZA®s
patent expiration in November 2017, which will, among other
things, provide funds to operate the company following the
completion of the asset sale;
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the implications of our existing net operating losses on the
potential after-tax value of the consideration to be received by
Ligand in the asset sale;
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the solicitation and bid process undertaken on behalf of the
company which resulted in Kings offer to acquire the
AVINZA®
assets;
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the recommendation of the strategic alternatives committee (a
committee formed to consider strategic alternatives available to
the company and make recommendations to the board of directors
regarding the companys strategic alternatives) to approve
the asset purchase agreement and recommend that our stockholders
vote for the approval of the asset sale and adoption
of the asset purchase agreement;
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historical, current and projected information concerning the
AVINZA®
business, financial performance and condition, operations,
technology, management and competitive position, and current
industry, economic and market conditions, including the
possibility that we continue to operate the
AVINZA®
business, shut down certain operations or sell other business
assets;
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the financial presentation of our financial advisor, UBS,
including its opinion (the full text of which is attached as
Annex B to this proxy statement), dated September 6,
2006, to the board of directors as to the fairness, from a
financial point of view and as of the date of the opinion, to
Ligand of the aggregate consideration to be received by Ligand
in the asset sale, as more fully described below under the
caption THE ASSET SALE Opinion of Our
Financial Advisor beginning on page 23;
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21
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the potential impact of the asset sale on our reputation,
customers, strategic partners and employees;
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Kings agreement to hire our sales representatives whose
primary responsibility is the promotion of
AVINZA®;
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Kings premier sales force and its ability to
promote AVINZA®,
and the impact of such promotion will have on the royalty
payments we will be entitled to under the asset purchase
agreement;
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the Contract Sales Force Agreement, referred to herein as the
contract sales agreement, with King, pursuant to
which King agreed to conduct a detailing program to promote the
sale of
AVINZA®
for an agreed upon fee, subject to the terms and conditions of
the contract sales agreement, which commenced on October 1,
2006 and is scheduled to continue for a period of six months or
until the closing of the asset sale or earlier termination of
the asset purchase agreement. Previously, Organon
Pharmaceuticals USA, Inc., conducted a detailing program to
promote the sale of
AVINZA®,
however, Organons ceased on September 30, 2006,
pursuant to and in accordance with the terms of Termination and
Return of Rights Agreement, dated as of January 1, 2006, by
and between Ligand and Organon Pharmaceuticals USA, Inc., which
would have resulted in the under promotion of
AVINZA®
if not for the contract sales agreement;
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the fact that the asset purchase agreement affords our board of
directors flexibility to consider, evaluate and accept superior
proposals in the period after signing and prior to the
consummation of the asset purchase agreement as follows:
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º
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subject to compliance with the asset purchase agreement, we can
participate in any discussions or negotiations with, and provide
any non-public information (other than any confidential
information of King or any non-public financial or other
material terms of the asset purchase agreement) to, any person
in response to an acquisition proposal by any such person, if
our board of directors determines that there is a reasonable
likelihood that such acquisition proposal could lead to a
superior proposal, as defined in the asset purchase agreement;
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º
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subject to compliance with the asset purchase agreement, our
board of directors is permitted to change its recommendation to
stockholders with respect to or enter into an alternative
transaction that is a superior proposal, conditioned upon the
payment to King of a $12 million termination fee;
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º
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subject to compliance with the asset purchase agreement, our
board of directors is permitted to change its recommendation to
stockholders, if it determines that doing so is consistent with
its fiduciary duties to our stockholders under applicable
law; and
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º
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subject to compliance with the asset purchase agreement, our
board of directors is permitted to take and disclose to our
stockholders a position with respect to any tender offer or
exchange offer by a third party or amend or withdraw such a
position in accordance with applicable law;
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our efforts, with the assistance of our advisors, to negotiate
and execute an asset purchase agreement favorable to us.
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In the course of its deliberations, the board of directors also
considered a variety of risks and other countervailing factors
concerning the asset purchase agreement and asset sale. The
material factors considered by the board of directors were:
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the risk that the asset sale might not be completed in a timely
manner or at all;
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the fact that our participation in any future earnings or growth
of
AVINZA®
will be limited to royalty payments;
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the restrictions on the conduct of our business prior to
completion of the asset sale, requiring us to conduct our
business only in the ordinary course, subject to specific
limitations or Kings consent, which may delay or prevent
us from undertaking business opportunities that may arise
pending completion of the asset sale;
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the restrictions on our board of directors ability to
solicit or engage in discussions or negotiations with a third
party regarding alternative transactions involving
AVINZA®
or Ligand as a whole, and the requirement
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22
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that we pay King a $12 million termination fee in certain
cases in the event of a termination of the asset purchase
agreement;
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the risk that the inventory adjustments required under the King
proposal could be substantial, thus reducing the up-front cash
consideration;
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the fact that we selected the King proposal over an alternative
proposal which offered consideration consisting of a larger
up-front cash payment coupled with a smaller royalty payment;
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the risk of diverting management focus and resources from other
strategic opportunities and from operational matters while
working to implement the asset sale; and
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the possibility of management and employee disruption associated
with the asset sale.
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The foregoing discussion of the material information and factors
considered by our board of directors. The board of directors
collectively reached a unanimous conclusion to recommend the
approval of the asset sale and adoption of the asset purchase
agreement in light of the various factors and other factors that
each member of the board of directors believed were appropriate.
In of the variety of factors considered by the board of
directors in connection with its evaluation of the asset sale
and the complexity of these matters, the board of directors did
not consider it practicable, and did not attempt, to quantify,
rank or otherwise assign relative or specific weight or values
to any of these factors. Rather, the board of directors made its
recommendation based on the totality of information presented to
it and the investigation conducted by it. In considering the
factors discussed above, individual directors may have given
different weight to different factors.
Recommendation
of Our Board of Directors
After careful consideration, our board of directors unanimously
determined that the asset sale is fair to, and in the best
interests of, the company and our stockholders and that the
asset purchase agreement and the asset sale are advisable.
Accordingly, our board of directors approved the asset purchase
agreement and recommended that our stockholders approve the
asset sale.
THE BOARD OF DIRECTORS UNANIMOUSLY RECOMMENDS THAT YOU VOTE
FOR THE APPROVAL OF THE ASSET SALE.
Opinion
of Our Financial Advisor
On September 6, 2006, at a meeting of our board of
directors held to evaluate the asset sale, UBS delivered to our
board of directors an oral opinion, confirmed by delivery of a
written opinion dated September 6, 2006, to the effect
that, as of that date and based on and subject to various
assumptions, matters considered and limitations described in its
opinion, the aggregate consideration to be received by Ligand in
the transaction was fair, from a financial point of view, to
Ligand.
The full text of UBS opinion describes the assumptions
made, procedures followed, matters considered and limitations on
the review undertaken by UBS. This opinion is attached as
Annex B and is incorporated into this proxy statement by
reference. UBS opinion is directed only to the
fairness, from a financial point of view, of the aggregate
consideration to be received by Ligand in the transaction and
does not address any other aspect of the transaction. The
opinion does not address the relative merits of the transaction
as compared to other business strategies or transactions that
might be available with respect to Ligands rights in
AVINZA®
and assets to be sold in the asset sale, collectively referred
to in this section as the
AVINZA®
assets, or Ligands underlying business decision to effect
the transaction. The opinion does not constitute a
recommendation to any stockholder as to how such stockholder
should vote or act with respect to the transaction. Holders of
our common stock are encouraged to read this opinion carefully
in its entirety. The summary of UBS opinion described
below is qualified in its entirety by reference to the full text
of its opinion.
In arriving at its opinion, UBS:
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reviewed publicly available business and financial information
relating to the
AVINZA®
assets and King;
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23
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reviewed internal financial information and other data relating
to the
AVINZA®
assets that were provided to UBS by Ligands management and
not publicly available, including financial forecasts and
estimates (including forecasts and estimates as to net sales
anticipated by Ligands management to be achieved by King)
prepared by Ligands management;
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conducted discussions with members of Ligands senior
management concerning the
AVINZA®
assets;
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reviewed publicly available financial and stock market data with
respect to companies UBS believed to be generally relevant;
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compared the financial terms of the transaction with the
publicly available financial terms of other transactions which
UBS believed to be generally relevant;
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reviewed the purchase agreement and certain related
documents; and
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conducted other financial studies, analyses and investigations,
and considered other information, as UBS deemed necessary or
appropriate.
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In connection with its review, with Ligands consent, UBS
did not assume any responsibility for independent verification
of any of the information provided to or reviewed by UBS for the
purpose of its opinion and, with Ligands consent, UBS
relied on that information being complete and accurate in all
material respects. In addition, with Ligands consent, UBS
did not make any independent evaluation or appraisal of any
assets, including the
AVINZA®
assets, or liabilities, contingent or otherwise, of Ligand, and
UBS was not furnished with any evaluation or appraisal. With
respect to the financial forecasts and estimates (including
forecasts and estimates as to net sales) prepared by
Ligands management, UBS assumed, at Ligands
direction, that they were reasonably prepared on a basis
reflecting the best currently available estimates and judgments
of Ligands management as to the future performance of the
AVINZA®
assets and as to net sales. In addition, UBS assumed, with your
approval, that the forecasts and estimates as to net sales
anticipated by Ligands management to be achieved by King
will be achieved at the times and in the amounts projected. UBS
also relied, at Ligands direction, without independent
verification or investigation, upon the assessments of
Ligands management as to the
AVINZA®
assets and the risks associated with the
AVINZA®
assets (including the potential impact of drug competition).
UBS opinion was necessarily based on economic, monetary,
market and other conditions as in effect on, and the information
available to UBS as of, the date of its opinion.
At Ligands direction, UBS contacted third parties to
solicit indications of interest in a possible transaction with
Ligand and held discussions with certain of these parties prior
to the date of UBS opinion. At Ligands direction,
UBS was not asked to, and it did not, offer any opinion as to
the terms of the transaction agreement or any related documents,
other than the aggregate consideration to be received by Ligand
in the transaction to the extent expressly specified in the
opinion, or the form of the transaction. In rendering its
opinion, UBS assumed, with Ligands consent, that Ligand,
King and King R&D would comply with all material terms of
the purchase agreement and related documents and that the
transaction would be consummated in accordance with the terms of
the purchase agreement and related documents without any adverse
waiver or amendment of any material term or condition of the
purchase agreement or related documents. UBS also assumed that
all governmental, regulatory or other consents and approvals
necessary for the consummation of the transaction would be
obtained without any material adverse effect on the
AVINZA®
assets, Ligand, King or the transaction. Except as described
above, Ligand imposed no other instructions or limitations on
UBS with respect to the investigations made or the procedures
followed by UBS in rendering its opinion.
In connection with rendering its opinion to our board of
directors, UBS performed a variety of financial and comparative
analyses which are summarized below. The following summary is
not a complete description of all analyses performed and factors
considered by UBS in connection with its opinion. The
preparation of a financial opinion is a complex process
involving subjective judgments and is not necessarily
susceptible to partial analysis or summary description. With
respect to the selected companies analysis and the selected
transactions analysis summarized below, no company or
transaction used as a comparison is identical or directly
comparable to the
AVINZA®
assets or the transaction. These analyses necessarily involve
complex considerations and judgments concerning financial and
operating characteristics and other factors that could affect
the public trading or acquisition values of the companies or
businesses concerned.
24
UBS believes that its analyses and the summary below must be
considered as a whole and that selecting portions of its
analyses and factors or focusing on information presented in
tabular format, without considering all analyses and factors or
the narrative description of the analyses, could create a
misleading or incomplete view of the processes underlying
UBS analyses and opinion. None of the analyses performed
by UBS was assigned greater significance or reliance by UBS than
any other. UBS arrived at its ultimate opinion based on the
results of all analyses undertaken by it and assessed as a
whole. UBS did not draw, in isolation, conclusions from or with
regard to any one factor or method of analysis for purposes of
its opinion.
The estimates of the future performance of the
AVINZA®
assets and estimates of net sales provided by Ligands
management in or underlying UBS analyses are not
necessarily indicative of future results or values, which may be
significantly more or less favorable than those estimates. In
performing its analyses, UBS considered industry performance,
general business and economic conditions and other matters, many
of which are beyond the control of Ligand. Estimates of the
financial value of companies, businesses or product lines do not
necessarily purport to be appraisals or reflect the prices at
which such companies, businesses or product lines actually may
be sold.
The aggregate consideration was determined through negotiation
between Ligand and King and the decision to enter into the
transaction was solely that of Ligands board of directors.
UBS opinion and financial analyses were only one of many
factors considered by Ligands board in its evaluation of
the transaction and should not be viewed as determinative of the
views of Ligands board of directors or management with
respect to the transaction or the aggregate consideration.
The following is a brief summary of the material financial
analyses performed by UBS and reviewed with Ligands board
of directors in connection with its opinion relating to the
asset sale. The financial analyses summarized below include
information presented in tabular format. In order to fully
understand UBS financial analyses, the tables must be read
together with the text of each summary. The tables alone do not
constitute a complete description of the financial analyses.
Considering the data below without considering the full
narrative description of the financial analyses, including the
methodologies and assumptions underlying the analyses, could
create a misleading or incomplete view of UBS financial
analyses. For purposes of the analyses described below, the
term implied value of the aggregate consideration
refers to the implied value of the aggregate consideration to be
received by Ligand in the transaction based on the initial
consideration of $312.75 million, consisting of
$265.0 million in cash and the assumption of Ligands
payment obligation of $47.75 million to Organon
Pharmaceuticals USA Inc. (or reimbursement to Ligand of such
amount to the extent paid by Ligand prior to the closing of the
asset sale) plus the estimated net present value of future
royalty payments payable to Ligand derived utilizing internal
estimates of Ligands management as to net sales of
AVINZA®
that will be achieved by King and a discount rate of 13.5%.
Selected
Companies Analysis
UBS compared selected standalone financial data for the
AVINZA®
assets with corresponding data for the following six publicly
traded specialty pharmaceuticals companies:
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Axcan Pharma Inc.
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Bradley Pharmaceuticals, Inc.
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Connetics Corporation
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Pharmion Corporation
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Salix Pharmaceuticals, Ltd.
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Sciele Pharma, Inc.
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UBS reviewed, among other things, enterprise values of the
selected companies, calculated as equity market value based on
closing stock prices on September 1, 2006, plus book value
of debt and minority interests, plus preferred stock, less cash,
as a multiple of latest 12 months revenue and calendar years
2006 and 2007 estimated revenue. UBS then compared the latest
12 months revenue and calendar years 2006 and 2007
estimated revenue
25
multiples derived from the selected companies with corresponding
multiples implied for the
AVINZA®
assets based on the implied value of the aggregate
consideration. Financial data of the selected companies were
based on publicly available research analysts estimates,
public filings and other publicly available information.
Financial data relating to the
AVINZA®
assets were based on public filings and internal estimates of
Ligands management. This analysis indicated the following
implied high, mean, median and low multiples for the selected
companies, as compared to corresponding multiples implied for
the
AVINZA®
assets based on the implied value of the aggregate consideration:
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Implied Multiples for
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Implied Multiples
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AVINZA®
Assets Based on
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for Selected Companies
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Implied Value of Aggregate
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Enterprise Value as Multiple of:
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High
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Mean
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Median
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Low
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Consideration
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Revenue
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Latest 12 Months
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3.1
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x
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2.3
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x
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2.2
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x
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1.8
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x
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3.7x
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Calendar year 2006
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2.8
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x
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2.3
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x
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2.2
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x
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1.9
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x
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3.3x
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Calendar year 2007
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2.3
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x
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2.1
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x
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2.0
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x
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1.9
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x
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3.2x
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Selected
Transactions Analysis
UBS reviewed transaction values in the following 10 selected
transactions in the pharmaceuticals industry announced since
August 2000 involving the sale of one or more products:
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Acquiror
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Seller (Product)
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Valeant
Pharmaceuticals International
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InterMune, Inc.
(Infergen)
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Pfizer Inc.
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Sanofi-Synthelabo
(Campto)
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Connetics Corporation
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Hoffmann-La Roche
Inc. (Soriatane)
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Galen Holdings PLC
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Eli Lilly and Company
(Sarafem)
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Enzon, Inc.
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Elan Corporation, plc
(Abelcet)
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Schering AG
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Immunex Corporation
(Leukine)
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King
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Johnson &
Johnson (Ortho-Prefest)
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King
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Bristol-Myers Squibb
Company (Corgard, Corzide, Delestrogen and Florinef)
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Biovail Corporation
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Aventis
Pharmaceuticals Inc. (Cardizem)
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Hoffman-La Roche
Inc.
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SmithKline Beecham plc
(Kytril)
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UBS reviewed transaction values in the selected transactions as
a multiple of latest 12 months revenue. UBS then compared
the latest 12 months revenue multiples derived from the
selected transactions with the corresponding multiple implied
for the
AVINZA®
assets based on the implied value of the aggregate
consideration. Multiples for the selected transactions were
based on publicly available information at the time of
announcement of the relevant transaction. Financial data
relating to the
AVINZA®
assets were based on public filings. This analysis indicated the
following implied high, mean, median and low multiples for the
selected transactions, as compared to the corresponding multiple
implied for the
AVINZA®
assets based on the implied value of the aggregate consideration:
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Implied Multiple for
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Implied Multiples
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AVINZA®
Assets Based on
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for Selected Companies
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Implied Value of Aggregate
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Transaction Value as Multiple of:
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High
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Mean
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Median
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Low
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Consideration
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Latest 12 Months Revenue
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4.3
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x
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3.2
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x
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3.4
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x
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1.7
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x
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3.7x
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Discounted
Cash Flow Analysis
UBS performed a discounted cash flow analysis to calculate the
estimated present value of the standalone unlevered, after-tax
free cash flows that could be generated from the
AVINZA®
assets over the period beginning September 6, 2006 through
fiscal year 2020 based on internal estimates of Ligands
management. The cash flows were then discounted to present value
using discount rates ranging from 11.5% to 15.5%. This analysis
indicated the
26
following implied reference range for the
AVINZA®
assets, as compared to the implied value of the aggregate
consideration:
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Implied Reference Range for
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Implied Value of Aggregate
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AVINZA®
Assets
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Consideration
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$307.6 million -
$357.4 million
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$
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480.8 million
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Miscellaneous
Under the terms of UBS engagement, Ligand has agreed to
pay UBS for its financial advisory services in connection with
the transaction an aggregate fee of approximately
$4.5 million, a portion of which was payable in connection
with UBS opinion and a significant portion of which is
contingent upon completion of the transaction. In addition,
Ligand has agreed to reimburse UBS for its reasonable expenses,
including fees, disbursements and other charges of legal
counsel, and to indemnify UBS and related parties against
liabilities, including liabilities under federal securities
laws, relating to, or arising out of, its engagement. UBS in the
past has provided, and currently is providing, investment
banking services to Ligand unrelated to the asset sale,
including acting as financial advisor to Ligand in connection
with Ligands sale of its oncology product lines to Eisai
Co., Ltd., for which UBS received an aggregate fee of
approximately $2.1 million. In the past, UBS has provided
investment banking services to King unrelated to the asset sale,
for which UBS received compensation. In the ordinary course of
business, UBS, its successors and affiliates may hold or trade,
for their own accounts and the accounts of their customers,
securities of Ligand and King and, accordingly, may at any time
hold a long or short position in such securities.
Ligand selected UBS as its financial advisor in connection with
the transaction because UBS is an internationally recognized
investment banking firm with substantial experience in similar
transactions and is familiar with Ligand and its business. UBS
is continually engaged in the valuation of businesses and their
securities in connection with mergers and acquisitions,
leveraged buyouts, negotiated underwritings, competitive bids,
secondary distributions of listed and unlisted securities and
private placements.
Required
Vote
Approval of the asset sale requires the affirmative vote of the
holders of a majority of the outstanding shares of our common
stock entitled to vote at the special meeting. Each holder of a
share of our common stock is entitled to one vote per share.
Failure to vote by proxy (by returning a properly executed proxy
card or by following the instructions printed on the proxy card
for telephone and Internet voting) or to vote in person will not
count as votes cast or shares voting on the proposals.
Abstentions, however, will count for the purpose of determining
whether a quorum is present. Since the approval of the asset
sale requires the approval of the holders of a majority of our
shares outstanding, abstentions will have the same effect as
votes against the proposal. Broker non-votes and the
shares of common stock as to which a stockholder abstains are
included for purposes of determining whether a quorum of shares
of common stock is present at a meeting. A broker
non-vote occurs when a nominee holding shares of
common stock for the beneficial owner does not vote on a
particular proposal because the nominee does not have
discretionary voting power with respect to that item and has not
received instructions from the beneficial owner. Since the
approval of the asset sale requires the approval of the holders
of a majority of our shares outstanding, broker
non-votes will have the same effect as votes against
such proposal.
Proceeds
from the Asset Sale
While we are evaluating a distribution of a substantial portion
of the net cash proceeds from the asset sale to our stockholders
in the form of a special dividend, we cannot predict the timing
or amount of such distribution, if any, to be made to our
stockholders. The amount, if any, available to our stockholders
will be determined by our board of directors, after weighing the
companys remaining liabilities and operational needs.
Effects
of the Asset Sale
If the asset sale is approved and the purchase agreement is
adopted by our stockholders and the other conditions to closing
are satisfied, we expect to become a research and development
focused company with no
27
marketed products and we will consider all available
alternatives. Such alternatives may include, without limitation,
the acquisition of a new business or alternatively, the sale of
the company, the sale of additional assets, restructuring, the
distribution of assets to our stockholders or the possible
dissolution of us and liquidation of our assets, the discharge
of any remaining liabilities, and the eventual distribution of
the remaining assets to our stockholders in the event we are
liquidated. Furthermore, although we are evaluating a
distribution of a substantial portion of the net cash proceeds
from the asset sale to our stockholders in the form of a special
dividend, we have not determined the timing or amount of
distribution, if any, to be made to our stockholders. The
amount, if any, available to our stockholders will be determined
by our board of directors, after weighing the companys
remaining liabilities and operational needs.
Most of our products in development will also require extensive
additional development, including preclinical testing and human
studies, as well as regulatory approvals, before we can market
them. We cannot predict if or when any of the products we are
developing or those being developed with our partners will be
approved for marketing. Any product development failures for
these or other reasons, whether with our products or our
partners products, may reduce our expected revenues,
profits, and stock price.
The
AVINZA®
assets constitute approximately 67% of our revenues and 81% of
our operating loss in the first two quarters of fiscal 2006.
Following the asset sale, our immediate ability to produce
revenues and income will therefore be substantially reduced. As
such, the proceeds from the asset sale, along with other capital
that we have access to, may not be adequate to bring our
developing product lines to market, nor can we be certain that
our future products, even if brought to market, will be
sufficiently profitable to justify the sale of
AVINZA®.
In addition, under the asset purchase agreement, we have agreed
to indemnify King for a period of 16 months after the
closing for a number of specified matters including the breach
of our representations, warranties and covenants contained in
the asset purchase agreement, and in some cases for a period of
30 months following the closing of the asset sale. That
indemnification obligation could cause us to be liable to King
under certain circumstances, which would decrease the remaining
cash available for eventual distribution to stockholders or for
our use in connection with any future corporate purposes.
Additionally, the asset purchase agreement requires that King
assume specified liabilities related to the
AVINZA®
drug product. If King fails to perform and discharge the assumed
liabilities specified in the asset purchase agreement, then we
may be liable for the assumed liabilities which would also
decrease the remaining cash available for eventual distribution
to stockholders or for our use in connection with any future
corporate purposes.
Finally, we will continue to have an obligation to comply with
the applicable reporting requirements of the Securities Exchange
Act of 1934, as amended, even though compliance with such
reporting requirements is economically burdensome.
Purpose
of the Asset Sale
The purpose of the asset sale for Ligand is to enable it to
immediately realize the value of its remaining business. In this
respect, the board of directors believes that the asset sale is
more favorable to Ligands stockholders than any other
alternative reasonably available because of the uncertain
returns to such stockholders in light of Ligands business,
operations, financial condition, strategy and prospects, as well
as the risks involved in achieving those prospects, and general
industry, economic and market conditions, both on a historical
and on a prospective basis.
In particular, the board of directors believes that we face
several challenges in our efforts to increase stockholder value,
including competition from companies with substantially greater
scale. For these reasons, and the other reasons discussed under
The Asset Sale Reasons for the Asset
Sale beginning on page 21, the board of directors has
determined that the asset purchase agreement, the asset sale and
related transactions are advisable and are fair to and in the
best interests of Ligand and its stockholders.
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Other
Agreements and Transactions Related to the Asset Sale
Contract
Sales Force Agreement
On September 6, 2006, we entered into a Contract Sales
Force Agreement, referred to herein as the contract sales
agreement, with King, pursuant to which King agreed to
conduct a detailing program to promote the sale of
AVINZA®
for an agreed upon fee, subject to the terms and conditions of
the contract sales agreement. Pursuant to the contract sales
agreement, King has agreed to perform certain minimum monthly
product details, which commenced on October 1, 2006 and
continue for a period of six months or until the closing of the
asset sale or earlier termination is scheduled to the asset
purchase agreement. We estimate that, assuming the closing of
the asset sale were to occur at the end of December 2006, the
amount due to King under the contract sales agreement would be
approximately $4 million.
Loan Arrangement
In connection with the asset sale, King agreed to loan to us, at
our option, up to $37.75 million. On October 13, 2006
we entered into a loan agreement with King pursuant to which
King loaned to us $37.75 million at a 9.50% interest rate.
Pursuant to the loan agreement King took a security interest in
the
AVINZA®
assets as well as cash proceeds from the sale of our oncology
products equal to the loan amount. Upon closing of the asset
sale, accrued interest, if any, on the amount loaned by King to
us will be forgiven and the amount of the closing payment King
owes us under the asset purchase agreement will be increased by
the amount of the loan, including interest thereon, if any, and
an equal amount will be credited against that payment for
repayment of the loan. If the closing of the asset sale does not
occur, then the principal of the loan plus accrued interest will
become due on January 1, 2007.
Redemption
of 6% Notes
As a condition to the consummation of the asset purchase
agreement we are required, and on October 30, 2006, mailed
a notice of redemption to each of the holders of our
6% Convertible Subordinated Notes, due 2007, referred to
herein as the 6% Notes, the outstanding aggregate principal
amount of which, as of October 31, 2006, was approximately
$128 million. Pursuant to the notice of redemption each
outstanding 6% Note will be redeemed or converted on or
prior to November 29, 2006. For those notes that are not
converted into shares prior to the redemption date, we will pay
the holders of those notes a redemption price equal to 101.2% of
the outstanding principal amount plus accrued and unpaid
interest.
Other
Agreements and Transactions Related to our Strategic Review
Process
Sale
of Oncology Product Line to Eisai Inc. and Eisai Co.,
Ltd.
On September 7, 2006, we entered into an asset purchase
agreement with Eisai Inc. and Eisai Co., Ltd., pursuant to which
we agreed to sell to Eisai Inc. and Eisai Co., Ltd. all of our
rights to our four marketed oncology products:
ONTAK®,
Targretin®
capsules,
Targretin®
gel and
Panretin®
gel. In exchange for our interests in and to the oncology
products, Eisai Inc. and Eisai Co., Ltd. agreed to pay us an
aggregate up-front cash payment of $205 million,
$20 million of which will be funded into an escrow account
to support any indemnification claims made by Eisai following
the Closing, and Eisai will assume certain liabilities. On
October 25, 2006, we consummated the transactions described
above.
Sale
and Leaseback Transaction
On October 25, 2006, we entered into an asset purchase
agreement with Slough Estates USA Inc., for the sale of our
corporate headquarters building, the land it is on and two
adjacent undeveloped parcels for an aggregate consideration of
$47.6 million. Under the terms of the asset purchase
agreement, we will receive an up-front cash payment, net of
fees, expenses and payment of existing indebtedness of
approximately $35 million. In addition, we agreed to lease
back the building for a period of fifteen years, at a rate of
approximately $3 million per year, subject to a fixed
annual percentage increase as stated in the asset purchase
agreement. In addition, Ligand will have the right to extend the
term of the lease for two five year periods under the same terms
and conditions as the initial term. We currently expect these
transactions to close in November of 2006.
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Interests
of Our Directors and Executive Officers in the Asset
Sale
After the closing of the asset sale, King and King R&D have
agreed to indemnify and hold our executive officers and
directors from any loss arising out of any breach of
representations and warranties by King or King R&D, or a
failure by King or King R&D to perform covenants applicable
to them under the asset purchase agreement. All of our directors
and executive officers own shares of our common stock
and/or
options to purchase shares of our common stock, and to that
extent, their interests in the asset sale is the same as that of
other holders of our common stock. See Security Ownership
of Certain Beneficial Owners, Directors and Management
beginning on page 87.
Dissenters
Rights
Holders of our common stock will not have appraisal or
dissenters rights in connection with the asset sale.
Neither the Delaware General Corporation Law nor our certificate
of incorporation provides our stockholders with appraisal or
dissenters rights in connection with the asset sale. Our
shares of common stock will remain publicly traded on the Nasdaq
Global Market following the consummation of the asset sale.
Accounting
Treatment of the Asset Sale
Under accounting principles generally accepted in the United
States of America, upon stockholder approval of the asset
purchase agreement, we expect to reflect the results of
operations of the
AVINZA®
assets sold as discontinued operations, including the related
gain on the sale, net of any applicable taxes commencing with
the quarter during which the asset sale is probable of occurring
and is approved by the shareholders. For further information,
see the unaudited pro forma condensed financial information
included in this proxy statement.
Financing;
Source and Amount of Funds
The asset sale is not conditioned upon King obtaining financing.
The total amount of funds necessary to pay the initial asset
sale consideration will be approximately $312.75 million.
King expects to fund the transaction from its working capital.
MATERIAL
U.S. FEDERAL AND STATE INCOME TAX CONSEQUENCES
The asset sale will not result in any U.S. federal income
tax consequences to our stockholders. The transaction will be a
taxable event to Ligand for U.S. federal income tax
purposes, but Ligand anticipates that a substantial portion or
all of the taxable gain resulting from the asset sale will be
offset by net operating losses. However, the asset sale is
expected to result in some federal alternative minimum tax being
imposed on Ligand in the year of the sale and may, depending
upon several factors, result in the imposition of federal income
taxes in subsequent years that may or may not be offset by
available tax credits. In addition, assuming net operating
losses are used to offset gain recognized on Ligands other
asset dispositions, Ligand expects that all or substantially all
of the taxable gain resulting from the asset sale will be
subject to state income tax, which may be substantially reduced
if Ligand is able to substantiate and claim certain tax credits.
The asset sale also may result in Ligand being subject to state
or local sales, use or other taxes in jurisdictions in which
Ligand files tax returns or has assets.
REGULATORY
MATTERS
The asset sale is subject to the HSR Act, which provides that
certain acquisition transactions may not be consummated unless
certain acquisition transactions may not be consummated unless
certain information has been furnished to the Antitrust Division
of the Department of Justice, which we refer to as the DOJ, and
the Federal Trade Commission, which we refer to as the FTC, and
certain waiting period requirements have been satisfied.
Pursuant to the HSR Act, on September 13, 2006, each of
Ligand and King filed a Notification and Report Form for Certain
Mergers and Acquisitions in connection with the asset sale with
the DOJ and FTC. On October 5, 2006, we were notified that
we had been granted early termination of the waiting period
under the HSR Act.
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ASSET
PURCHASE AGREEMENT
The following is a summary of the material terms of the asset
purchase agreement. This summary does not purport to describe
all the terms of the asset purchase agreement and is qualified
by reference to the complete asset purchase agreement, which is
attached as Annex A to this proxy statement. We urge you to
read the asset purchase agreement carefully and in its entirety
because it, and not this proxy statement, is the legal document
that governs the asset sale.
The text of the asset purchase agreement has been included to
provide you with information regarding its terms. The terms of
the asset purchase agreement (such as the representations and
warranties) are intended to govern the contractual rights and
relationships, and allocate risks, between the parties in
relation to the asset sale. The asset purchase agreement
contains representations and warranties that Ligand, on the one
hand, and King and King R&D on the other hand, made to each
other as of specific dates. The representations and warranties
were negotiated between the parties with the principal purpose
of setting forth their respective rights with respect to their
obligations to consummate the asset sale and may be subject to
important limitations and qualifications as set forth therein,
including a contractual standard of materiality different from
that generally applicable under federal securities laws.
In addition, such representations and warranties are qualified
by information in confidential disclosure schedules that Ligand
and King have exchanged in connection with signing the asset
purchase agreement. While Ligand does not believe that the
disclosure schedules contain information that the securities
laws require to be publicly disclosed, the disclosure schedules
do contain information that modifies, qualifies and creates
exceptions to the representations and warranties set forth in
the attached asset purchase agreement. Accordingly, you should
not rely on the representations and warranties as
characterizations of the actual state of facts, since they are
modified by the underlying disclosure schedules. These
disclosure schedules contain information that has been included
in our prior public disclosures, as well as potential additional
non-public information. Moreover, information concerning the
subject matter of the representations and warranties may have
changed since the date of the asset purchase agreement, which
subsequent information may or may not be fully reflected in our
public disclosures.
General
Under the terms of the asset purchase agreement, King and King
R&D have agreed to purchase all of our United States, and
its territories and Canadian rights in and to
AVINZA®,
including, among other things, all
AVINZA®
inventory, equipment, records and related intellectual property.
Pursuant to the terms of the asset purchase agreement, King and
King R&D will make a $265 million cash payment to
Ligand, $15 million of which will be funded into an escrow
account to support any indemnifications claims made by King, to
acquire our rights in and to
AVINZA®.
In addition, King will assume a product-related liability
totaling approximately $48 million and future royalty
payments owed to Organon Pharmaceuticals USA Inc. and all other
existing product royalty obligations. In addition to existing
royalty obligations assumed by King, King will pay Ligand a 15%
royalty during the first 20 months after the closing of the
asset sale. Subsequent royalty payments will be based upon
calendar year net sales. If Kings calendar year net sales
are less than $200 million, the royalty payment will be 5%
of all of Kings net sales for that year. If Kings
calendar year net sales are greater than $200 million, then
the royalty payment will be 10% of all of Kings net sales
less than $250 million, plus 15% of all of Kings net
sales greater than $250 million.
Additionally, the $265 million cash payment from King and
King R&D may be offset by an inventory value adjustment. On
the closing date of the asset sale, we will provide King and
King R&D with a report based on our inventory data, which
will set forth (i) certain inventory calculations,
(ii) whether we have met certain specified reduction of
levels of inventory held by retailers and wholesalers, and
(iii) our
out-of-pocket
costs paid with respect to certain of our contracts related to
AVINZA®.
If, as of the closing of the asset sale, we have not reduced the
amount of inventory held by wholesalers and retailers, to the
agreed upon levels, King will have the right to the distribution
of such amounts from a special inventory escrow amount which
shall be funded at closing from the $265 million cash
proceeds.
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Closing
Closing of the asset sale under the asset purchase agreement
will occur on a date following the satisfaction or waiver of all
conditions to the obligations of the parties to consummate the
transactions contemplated thereby, including the approval of the
asset sale and adoption of the asset purchase agreement by the
holders of a majority of our common stock outstanding on the
record date.
Representations
and Warranties
The asset purchase agreement contains a number of customary
representations and warranties applicable to Ligand, subject in
some cases to customary qualifications, relating to, among other
things, the following:
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due organization, valid existence and good standing, and other
corporate matters of Ligand;
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authorization, execution, delivery and enforceability of the
asset purchase agreement;
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conflicts or violations under charter documents, contracts and
instruments or law;
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title to, or interest in, encumbrances upon and the sufficiency
of the properties and assets that are used to conduct our
AVINZA®
business;
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intellectual property matters;
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pending or threatened material litigation;
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required consents and approvals;
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taxes;
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matters related to employee benefits applicable to us;
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governmental registrations;
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material compliance with all applicable laws;
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regulatory matters;
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government contracts
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financial statements;
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matters related to product recalls, product returns, product
warranties and product liabilities;
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brokerage or finders fees, and other fees with respect to
the asset sale;
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inventory and equipment;
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contracts;
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product liability
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exporting and manufacturing;
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customers, suppliers and third-party service providers; and
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adverse event reports.
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The asset purchase agreement also contains a number of customary
representations and warranties applicable to King and King
R&D, subject in some cases to customary qualifications,
relating to, among other things, the following:
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due organization, valid existence and good standing, and other
corporate matters of King and King R&D;
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authorization, execution, delivery and enforceability of the
asset purchase agreement;
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conflicts or violations under charter documents, contracts and
instruments or law;
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pending or threatened material litigation;
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required consents and approvals;
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financing; and
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brokerage or finders fees, and other fees with respect to
the asset sale.
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The representations and warranties of each of the parties to the
asset purchase agreement will expire upon completion of the
asset sale.
Indemnification;
Survival of Indemnification Obligations
After closing of the asset sale, we have agreed to indemnify and
hold King and its affiliates and their respective officers,
directors, employees, stockholders, agents, and representatives
harmless from any loss arising out of (i) any breach of
representations and warranties by us, (ii) our activities
before closing of the asset sale, (iii) a failure by us to
perform covenants applicable to us under the asset purchase
agreement, (iv) any liability not undertaken by King and
King R&D pursuant to the asset purchase agreement, or
(v) fees owed by us to any broker, financial advisor, or
others retained by us in connection with the asset sale. In
general, we may be required to indemnify King and King R&D
for any indemnifiable losses incurred by them in connection with
the asset sale for a period of 16 months following the
closing date of the asset sale, except that King may bring a
claim relating to a breach of representations and warranties
relating to the authorization, execution and delivery of the
asset purchase agreement, title to and sufficiency of assets,
and employee benefits for a period of 30 months following
the closing date of the asset sale. In general, we are not
obligated to make King whole for any losses until King suffers
losses in excess of $1.5 million and then only to the
extent such losses exceed $1.5 million. In addition, our
liability for any claim for indemnification brought by King or
King R&D is limited to $40 million. Pursuant to the
asset purchase agreement, $15 million of the cash payment
to be made by King to us at the closing of the asset sale will
be funded into an escrow account to support any indemnification
claims made by King. If no claims are made by King as of the one
year anniversary of the closing of the asset sale, the escrow
amount will be released to Ligand.
After closing of the asset sale, King and King R&D have
agreed to indemnify and hold us and our affiliates, and our
respective officers, directors, employees, stockholders, agents,
and representatives harmless from any loss arising out of
(i) any breach of representations and warranties by King or
King R&D, (ii) or a failure by King or King R&D to
perform covenants applicable to them under the asset purchase
agreement, (iii) any liability assumed by King and King
R&D under the asset purchase agreement, or (iv) fees
owed by King or King R&D to any broker, financial advisor,
or others retained by them in connection with the asset sale.
Covenants
and Agreements
Under the asset purchase agreement, we have agreed to abide by
certain customary covenants prior to the closing of the asset
sale. Among others, these covenants include the following:
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permitting representatives of King to have reasonable access to
all premises, personnel, personnel records, other records and
contracts of Ligand with respect to
AVINZA®;
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providing certain reports to King regarding inventory;
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operating the
AVINZA®
business in the ordinary course, preserving the
AVINZA®
business substantially intact, and preserving the goodwill of
those third parties having business relationships with us;
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using our best efforts to reduce inventory to achieve specified
levels in the wholesale and retail channels;
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paying all taxes and payables;
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making all filings required to consummate the asset sale;
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preparing and filing this proxy statement, soliciting proxies
from our stockholders in favor of the approval of the asset sale
and adoption of the asset purchase agreement, and holding the
special meeting to which this proxy statement relates;
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mailing to each of the holders of our convertible notes a notice
of redemption;
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using commercially reasonable efforts to facilitate an efficient
transfer of
AVINZA®
to Buyer.
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We have agreed to promptly notify King following any material
developments or changes with respect to
AVINZA®
or upon becoming aware of any event arising after the date of
the asset purchase agreement that would result in any material
breach of our representations, warranties or covenants or that
would have the effect of making any representation or warranty
untrue or incorrect in any material respect so as to cause the
failure of any closing conditions. In addition, we have also
agreed that until the consummation of the asset sale, subject to
certain exceptions for actions taken in the ordinary course of
business or actions contemplated by the asset purchase
agreement, consistent with past practice, we will comply with
specific restrictions relating to, among others:
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taking any willful action likely to result in any material
representation or warranty becoming untrue;
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creating any encumbrance on our properties;
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entering into any contracts relating primarily or exclusively to
AVINZA®;
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terminating any of the contracts to e assigned to King pursuant
to the asset purchase agreement;
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transferring or granting any rights related to
AVINZA®,
including any intellectual property rights;
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failing to renew specified contracts;
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initiating any litigation or arbitration actions, or make any
claims or demands for breach with respect to specified contracts;
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entering into or modifying employment agreements with certain
employees, or modifying the job descriptions of such
employees; or
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agreeing to take any of the actions specified in the previous
bullet points.
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Regulatory
Matters
The asset purchase agreement provides that we and King will file
as soon as practicable after the date of the asset purchase
agreement any required filings and applications with
governmental authorities in connection with the asset sale,
including filings under the HSR Act.
No
Negotiation
The asset purchase agreement provides that Ligand shall not, nor
shall it cause any of its affiliates or representatives to,
directly or indirectly, take any action to:
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solicit, initiate or facilitate any acquisition proposal (as
described below);
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participate in any discussions or negotiations with, or furnish
any non-public information to, any third party that has made an
acquisition proposal; or
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enter into any agreement with respect to any acquisition
proposal.
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So long as we provide notice to King, at any time prior to the
closing of the asset sale, we are permitted to:
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participate in any discussions or negotiations with, and with
certain exceptions, provide any non-public information to, any
third party in response to an acquisition proposal by such third
party, if our board of directors determines that there is a
reasonable likelihood that such acquisition proposal could lead
to a superior proposal (as described below);
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enter into an agreement with respect to an acquisition proposal
if our board of directors determines that such acquisition
proposal constitutes a superior proposal; and
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effect a change in the recommendation of our board of directors
regarding the asset purchase agreement and asset sale, if our
board of directors determines that (i) such acquisition
proposal constitutes a superior
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proposal or (ii) failure to take such action would be
inconsistent with the boards fiduciary duties under
Delaware law; and
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The prohibition on solicitation does not prevent Ligand or our
board of directors from complying with SEC rules with regard to
an acquisition proposal by means of a tender offer or
recommending or exploring an acquisition proposal if the board
determines in good faith that an unsolicited acquisition
proposal is reasonably likely to lead to a superior proposal and
that, after consultation with its legal advisor, failure to take
such action would be inconsistent with its fiduciary duties
under Delaware law.
As described in this proxy statement, the term acquisition
proposal means an unsolicited proposal from a third party
relating to any transaction involving, in whole or in part,
directly or directly,
AVINZA®,
including an acquisition of more than 25% of our common stock.
The term superior proposal means an acquisition
proposal which (a) as determined in good faith by our board
of directors (after consultation with Ligands financial
advisor and outside legal counsel) would, if consummated,
(i) result in a transaction more favorable to us than the
asset sale, if such transaction is for the acquisition of
AVINZA®,
or (ii) result in a transaction more favorable to our
stockholders than the asset sale if such transaction is for the
acquisition of equity interests in Ligand or substantially all
of our assets, or (b) does not require the termination of
the asset purchase agreement as a condition to the consummation
of such acquisition proposal. If we enter into an agreement with
any third party with respect to a superior proposal, we will be
required to pay the termination fee of $12 million. See
The Asset Purchase Agreement Termination
Fee beginning on page.
Conditions
to Completion of the Asset Sale
The obligations of Ligand and King and King R&D to complete
the asset sale are subject to the satisfaction or waiver of the
following conditions:
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|
no preliminary or permanent injunction or other order has been
issued by any court or by any government authority enjoining,
restraining, prohibiting or making illegal the asset sale;
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|
any waiting period (and any extension) under the HSR Act has
expired or been terminated; and
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|
the Ligand stockholders have adopted resolutions approving the
asset sale and adopting the asset purchase agreement.
|
In addition, the obligations of King and King R&D to
complete the asset sale are subject to the satisfaction by
Ligand or waiver by King or King R&D of conditions,
including the following:
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Ligands representations and warranties shall be true and
correct in all material respects as of the date of the asset
purchase agreement and the date of the closing of the asset
sale, except those representations and warranties which address
matters only as of a particular date need only be true and
correct as of such date;
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Ligand shall have performed and complied in all material
respects with each of the covenants, agreements and obligations
Ligand is required to perform under the asset purchase agreement;
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all specified consents shall have been duly executed and
delivered to King or King R&D;
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King or King R&D shall have received a certificate from us
certifying the accuracy of our representations and warranties
and performance of our obligations as of the date of the asset
purchase agreement and the closing date of the asset sale;
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Ligand shall have executed and delivered to King or King R&D
each of the following agreements: the Assignment of Product
Intellectual Property, the Bill of Sale and Assignment and
Assumption Agreement, the Product License and Supply Agreement
Assignment, the Second Source Supply Agreement Assignment, the
Termination and Return of Rights Agreement Assignment, the
Technical Agreement
AVINZA®
Assignment, the Quality Agreement for
AVINZA®
Assignment, the Transition Services Agreement and the Escrow
Agreement; and
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Ligand shall have redeemed or converted all outstanding 6%
Convertible Subordinated Notes due 2007.
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35
In addition, the obligations of Ligand to complete the asset
sale are subject to the satisfaction by King and King R&D or
waiver by Ligand of conditions, including the following:
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Kings and King R&Ds representations and
warranties shall be true and correct in all material respects as
of the date of the asset purchase agreement and the date of the
closing of the asset sale, except those representations and
warranties which address matters only as of a particular date
need only be true and correct as of such date;
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King and King R&D shall have performed and complied in all
material respects with each of the covenants, agreements and
obligations King and King R&D are required to perform under
the asset purchase agreement;
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Ligand shall have received a certificate from King and King
R&D certifying the accuracy of their representations and
warranties and performance of their obligations as of the date
of the asset purchase agreement and the closing date of the
asset sale; and
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King and King R&D shall have executed and delivered to
Ligand each of the following agreements: the Assignment of
Product Intellectual Property, the Bill of Sale and Assignment
and Assumption Agreement, the Product License and Supply
Agreement Assignment, the Second Source Supply Agreement
Assignment, the Termination and Return of Rights Agreement
Assignment, the Technical Agreement
AVINZA®
Assignment, the Quality Agreement for
AVINZA®
Assignment, the Transition Services Agreement and the Escrow
Agreement.
|
Termination
We and King may by mutual written consent terminate the asset
purchase agreement at any time prior to the completion of the
asset sale.
In addition, either we or King may, in writing, terminate the
asset purchase agreement at any time prior to the effective time
of the asset sale:
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if the asset sale has not been consummated on or before
December 31, 2006 so long as the failure to complete the
asset sale by such date is not the result of the failure of the
party seeking to terminate to comply with the terms of the asset
purchase agreement;
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if the adoption of the asset purchase agreement by our
stockholders has not been obtained at the special meeting or any
adjournment thereof by reason of the failure to obtain the
required vote; or
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if a material breach of any provision of the asset purchase
agreement has been committed by the other party, and such breach
has not been waived or cured within 60 days after written
notice.
|
We may terminate, in writing, the asset purchase agreement at
any time prior to the completion of the asset sale:
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if any representation or warranty of King shall have become
untrue in any material respect or King has materially breached
any covenant under the asset purchase agreement, and such breach
or misrepresentation is not capable of being cured prior to
December 31, 2006;
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if a material breach of any provision of the asset purchase
agreement has been committed by King, and such breach is not
cured by King within 10 days after receipt of written
notice, or in the reasonable determination of Ligand, is
incapable of being cured by King; or
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if our board of directors has determined that an acquisition
proposal is a superior proposal provided that we give King
written notice within two days of such determination and pay to
King the termination fee of $12 million.
|
36
King may terminate, in writing, the asset purchase agreement at
any time prior to the completion of the asset sale:
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|
|
if any representation or warranty of ours shall have become
untrue in any material respect or we have materially breached
any covenant under the asset purchase agreement, and such breach
or misrepresentation is not capable of being cured prior to
December 31, 2006;
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if a material breach of any provision of the asset purchase
agreement has been committed by us, and such breach is not cured
by us within 10 days after receipt of written notice, or in
the reasonable determination of King, is incapable of being
cured by us;
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if, prior to the adoption of the asset purchase agreement by our
stockholders, our board of directors (i) fails to include
in this proxy statement its recommendation of the asset purchase
agreement or (ii) approves or recommends an acquisition
proposal to our stockholders or approves or recommends that our
stockholders tender their shares of our common stock in any
tender offer or exchange offer that is an acquisition
proposal; or
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|
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|
if King has received written notice from us that our board of
directors has determined that an acquisition proposal is a
superior proposal.
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Termination
Fee
We will be obligated to pay King a fee of $12 million in
connection with the termination of the asset purchase agreement
in the event that:
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if, prior to the receipt of requisite stockholder approval, King
terminates the asset purchase agreement as a result of our board
of directors:
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approving or recommending an acquisition proposal to Ligand
stockholders or approving or recommending that Ligand
stockholders tender their shares of common stock in any tender
offer or exchange offer that is an acquisition proposal; or
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|
|
|
failing to include in this proxy statement its recommendation
that our stockholders should approve the asset sale;
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|
|
|
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if King terminates the asset purchase agreement after receiving
written notice from us that our board of directors has
determined that an alternative acquisition proposal is a
superior proposal; or
|
|
|
|
if we terminate the asset purchase agreement as a result of our
board of directors determining that an alternative acquisition
proposal is a superior proposal.
|
Expenses
The asset purchase agreement provides that other than any
antitrust filing fees, which shall be shared equally by Ligand
and King, all costs and expenses incurred in connection with the
asset purchase agreement and the transactions contemplated by
the asset purchase agreement will be paid by the party incurring
the expenses.
Amendment
The asset purchase agreement may be amended, supplemented, or
otherwise modified by the parties in writing at any time before
or after any approval of the asset purchase agreement by the
Ligand stockholders, but after the stockholder approval, no
amendment may be made for which the law requires stockholder
approval without such stockholder approval.
37
UNAUDITED
PRO FORMA CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
As described further in this Proxy Statement, on
September 6, 2006, the Company, King Pharmaceuticals, Inc.,
a Tennessee corporation, and King Pharmaceuticals Research and
Development, Inc., a Delaware corporation and wholly-owned
subsidiary of King Pharmaceuticals (together with King
Pharmaceuticals, King) entered into a purchase
agreement (the AVINZA Purchase Agreement), pursuant
to which King agreed to acquire all of the Companys rights
in and to
AVINZA®
(morphine sulfate extended-release capsules) in the United
States, its territories and Canada, including, among other
things, all
Avinza®
inventory, equipment, records and related intellectual property,
and assume certain liabilities (together, AVINZA or
the AVINZA Product Line) as set forth in the AVINZA
Purchase Agreement. Additionally, a condition of the AVINZA
Purchase Agreement requires that the Company redeem, prior to
the close of the sale of AVINZA to King, the outstanding
6% convertible subordinated notes, previously issued by the
Company (the Debt Redemption). Also, King will
assume certain liabilities, including certain product-related
liabilities owed by the Company to Organon Pharmaceuticals USA
Inc. Pursuant to the AVINZA Purchase Agreement, at closing, the
Company will be paid a $265.0 million cash payment,
$15.0 million of which will be funded into an escrow
account to support any indemnification claims. The Company
expects to account for the disposition of the AVINZA Product
Line as a discontinued operation in its consolidated financial
statements.
On September 7, 2006, the Company, Eisai Inc., a Delaware
corporation and Eisai Co., Ltd., a Japanese company (together
with Eisai Inc., Eisai), entered into a purchase
agreement (the Oncology Purchase Agreement) pursuant
to which Eisai has agreed to acquire all of the Companys
worldwide rights in and to the Companys oncology product
line, including, among other things, all related inventory,
equipment, records and intellectual property, and assume certain
liabilities (together Oncology or the Oncology
Product Line) as set forth in the Oncology Purchase
Agreement. The Oncology Product Line includes the Companys
four marketed oncology drugs: ONTAK, Targretin capsules,
Targretin gel and Panretin gel. Pursuant to the Oncology
Purchase Agreement, at closing, the Company will be paid a
$205.0 million cash payment, $20.0 million of which
will be funded into an escrow account to support any
indemnification claims. On October 25, 2006, the Company
consummated the sale of Oncology. The Company expects to account
for the disposition of the Oncology Product Line as a
discontinued operation in its consolidated financial statements.
On October 25, 2006, the Company entered into an agreement
with Slough Estates USA, Inc. (the Buyer) to sell
the real properties at its corporate headquarters located in
San Diego, California (the Sale Leaseback) .
Under the terms of the agreement, the Buyer has agreed to
purchase all real properties (land, building and improvements)
known as 10275 Science Center Drive, 10265 Science Center Drive
and 10285 Science Center Drive in San Diego, California for
a purchase price of approximately $47.6 million. In
addition, the Company is leasing back the building at 10275
Science Center Drive from the Buyer as its corporate
headquarters office, with a lease term of fifteen years through
2021. Under the terms of the lease, the Company will pay a basic
annual rent, which is subject to an annual fixed percentage
increase, and management fees, property taxes and other
necessary expenses associated with the lease. As a condition of
the sale, the Company will pay off its outstanding mortgage for
the property. The transaction is expected to close on or before
November 27, 2006.
The following unaudited pro forma condensed consolidated
financial statements illustrate the effects of the
Companys proposed sale of AVINZA and consummated sale of
Oncology, the Debt Redemption, which is a requirement of the
proposed sale of AVINZA, and the Sale Leaseback (together, the
Transactions), The Transactions have not yet been
fully reflected in the Companys historical financial
statements.
The unaudited pro forma condensed consolidated balance sheet as
of June 30, 2006 gives effect to the Transactions as if
they occurred as of that date. The unaudited pro forma condensed
consolidated statements of operations give effect to the Sale
Leaseback as if it occurred on January 1, 2005 and give
effect to the sales of AVINZA and Oncology as if they occurred
on January 1, 2003, as they are expected to be reported as
discontinued operations in the Companys consolidated
financial statements. The Sale Leaseback has not been reflected
in the unaudited pro forma condensed consolidated statements of
operations for the years ended December 31, 2004 and 2003,
as it will not be reported as a discontinued operation in the
Companys consolidated financial statements. The unaudited
pro forma condensed consolidated financial statements have been
derived from, and should be read in conjunction with the
Companys historical consolidated financial statements,
including the notes thereto, in the
38
Companys Annual Report filed on
Form 10-K
for the year ended December 31, 2005 and Quarterly Report
filed on
Form 10-Q
for the quarter ended June 30, 2006. The unaudited pro
forma condensed consolidated financial statements are not
necessarily indicative of the financial position or results of
operations that would have been achieved had the Transactions
described above occurred on the dates indicated or that may be
expected to occur in the future as a result of such transactions.
The unaudited pro forma condensed consolidated balance sheet
reflects significant assets and liabilities associated with the
AVINZA and Oncology product lines that will remain for a period
of time with the Company subsequent to the proposed
dispositions. Accordingly, the unaudited pro forma condensed
consolidated balance sheet may not reflect the ongoing financial
position of the Company. The unaudited pro forma condensed
consolidated statements of operations exclude revenues and
expenses directly attributable to AVINZA and Oncology, the Debt
Redemption and the Sale Leaseback. As such, the unaudited pro
forma condensed consolidated statements of operations do not
reflect a reduction of general corporate allocations or other
non-direct costs which may be expected to occur as a result of
the Transactions.
The board of directors of the Company is evaluating the
distribution of a substantial portion of the net cash proceeds
from the asset sales to the Companys shareholders in the
form of a special dividend following the consummation of the
Transactions. Additionally, the Company is seeking shareholder
approval to modify its 2002 Stock Incentive Plan (the 2002
Plan) to allow equitable adjustments to be made to options
outstanding under the 2002 Plan in the event of a special cash
dividend. Assuming our stockholders approve the amendment to the
2002 Plan, any such adjustments to outstanding options would be
considered a modification and result in the recognition of
compensation expense in the Companys consolidated
statement of operations under the requirements of Statement of
Financial Accounting Standard No 123(R) Share-Based
Payment (SFAS 123(R)). Any such expense
could be material. The accompanying unaudited pro forma
condensed consolidated financial statements do not reflect
adjustments related to the potential special cash dividend or
modifications to the terms of outstanding stock options that may
occur in connection with such a dividend.
39
LIGAND
PHARMACEUTICALS INCORPORATED
Unaudited
Pro Forma Condensed Consolidated Balance Sheet
As
of June 30, 2006
(In thousands, except share data)
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|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pro Forma
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
After
|
|
|
|
|
|
Sale
|
|
|
|
|
|
|
As
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Leaseback
|
|
|
Pro Forma
|
|
|
|
Reported
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
as Adjusted
|
|
|
ASSETS
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Current assets:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents
|
|
$
|
41,615
|
|
|
$
|
54,926C
|
|
|
$
|
96,541
|
|
|
$
|
182,268C
|
|
|
$
|
47,642
|
)J
|
|
$
|
313,663
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(719
|
)J
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(11,669
|
)J
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(400
|
)J
|
|
|
|
|
Short-term investments
|
|
|
19,168
|
|
|
|
|
|
|
|
19,168
|
|
|
|
|
|
|
|
|
|
|
|
19,168
|
|
Accounts receivable, net
|
|
|
18,667
|
|
|
|
|
|
|
|
18,667
|
|
|
|
|
|
|
|
|
|
|
|
18,667
|
|
Current portion of inventories, net
|
|
|
8,467
|
|
|
|
(2,922
|
)A
|
|
|
5,545
|
|
|
|
(5,545
|
)B
|
|
|
|
|
|
|
|
|
Other current assets
|
|
|
25,986
|
|
|
|
(8,464
|
)D
|
|
|
17,522
|
|
|
|
(1,620
|
)D
|
|
|
|
|
|
|
15,902
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total current assets
|
|
|
113,903
|
|
|
|
43,540
|
|
|
|
157,443
|
|
|
|
175,103
|
|
|
|
34,854
|
|
|
|
367,400
|
|
Restricted investments
|
|
|
1,826
|
|
|
|
|
|
|
|
1,826
|
|
|
|
|
|
|
|
|
|
|
|
1,826
|
|
Long-term portion of inventories,
net
|
|
|
5,211
|
|
|
|
|
|
|
|
5,211
|
|
|
|
(5,211
|
)B
|
|
|
|
|
|
|
|
|
Property and equipment, net
|
|
|
21,561
|
|
|
|
(707
|
)A
|
|
|
20,854
|
|
|
|
(12
|
)B
|
|
|
(14,666
|
)J
|
|
|
6,176
|
|
Acquired technology, product rights
and royalty buy-down, net
|
|
|
139,766
|
|
|
|
(86,897
|
)A
|
|
|
52,869
|
|
|
|
(52,869
|
)B
|
|
|
|
|
|
|
|
|
Other assets
|
|
|
3,665
|
|
|
|
(1,358
|
)E
|
|
|
2,307
|
|
|
|
(2,176
|
)B
|
|
|
|
|
|
|
131
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total Assets
|
|
$
|
285,932
|
|
|
$
|
(45,422
|
)
|
|
$
|
240,510
|
|
|
$
|
114,835
|
|
|
$
|
20,188
|
|
|
$
|
375,533
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND
STOCKHOLDERS EQUITY (DEFICIT)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Current liabilities:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Accounts payable
|
|
$
|
19,460
|
|
|
$
|
|
|
|
$
|
19,460
|
|
|
$
|
|
|
|
$
|
|
|
|
$
|
19,460
|
|
Accrued liabilities
|
|
|
58,302
|
|
|
|
9,315
|
F
|
|
|
117,108
|
|
|
|
3,526
|
F
|
|
|
|
|
|
|
153,206
|
|
|
|
|
|
|
|
|
34,603
|
G
|
|
|
|
|
|
|
21,194
|
G
|
|
|
1,964
|
J
|
|
|
|
|
|
|
|
|
|
|
|
(961
|
)C
|
|
|
|
|
|
|
|
|
|
|
2,309
|
K
|
|
|
|
|
|
|
|
|
|
|
|
15,849
|
K
|
|
|
|
|
|
|
7,105
|
K
|
|
|
|
|
|
|
|
|
Current portion of deferred revenue
|
|
|
143,102
|
|
|
|
(107,537
|
)D
|
|
|
35,565
|
|
|
|
(35,565
|
)D
|
|
|
|
|
|
|
|
|
Current portion of co-promote
termination liability
|
|
|
45,046
|
|
|
|
(45,046
|
)A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Current portion of equipment
financing obligations
|
|
|
2,146
|
|
|
|
(251
|
)H
|
|
|
1,895
|
|
|
|
(8
|
)H
|
|
|
|
|
|
|
1,887
|
|
Current portion of long-term debt
|
|
|
356
|
|
|
|
|
|
|
|
356
|
|
|
|
|
|
|
|
(356
|
)J
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total current liabilities
|
|
|
268,412
|
|
|
|
(94,028
|
)
|
|
|
174,384
|
|
|
|
(3,748
|
)
|
|
|
3,917
|
|
|
|
174,553
|
|
Long-term debt
|
|
|
139,463
|
|
|
|
(128,150
|
)I
|
|
|
11,313
|
|
|
|
|
|
|
|
(11,313
|
)J
|
|
|
|
|
Long-term portion of co-promote
termination liability
|
|
|
94,261
|
|
|
|
(94,261
|
)A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Long-term portion of equipment
financing obligations
|
|
|
2,851
|
|
|
|
(251
|
)H
|
|
|
2,600
|
|
|
|
(14
|
)H
|
|
|
|
|
|
|
2,586
|
|
Long-term portion of deferred
revenue
|
|
|
4,100
|
|
|
|
|
|
|
|
4,100
|
|
|
|
(1,553
|
)D
|
|
|
|
|
|
|
2,547
|
|
Other long-term liabilities
|
|
|
3,002
|
|
|
|
|
|
|
|
3,002
|
|
|
|
(584
|
)B
|
|
|
27,498
|
J
|
|
|
29,916
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total liabilities
|
|
|
512,089
|
|
|
|
(316,690
|
)
|
|
|
195,399
|
|
|
|
(5,899
|
)
|
|
|
20,102
|
|
|
|
209,602
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Commitments and contingencies
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock subject to conditional
redemption; 997,568 shares issued and outstanding at
June 30, 2006
|
|
|
12,345
|
|
|
|
|
|
|
|
12,345
|
|
|
|
|
|
|
|
|
|
|
|
12,345
|
|
Stockholders equity (deficit):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Common stock, $0.001 par
value; 200,000,000 shares authorized;
77,730,044 shares issued at June 30, 2006
|
|
|
78
|
|
|
|
|
|
|
|
78
|
|
|
|
|
|
|
|
|
|
|
|
78
|
|
Additional paid-in capital
|
|
|
751,547
|
|
|
|
|
|
|
|
751,547
|
|
|
|
|
|
|
|
|
|
|
|
751,547
|
|
Accumulated other comprehensive
income
|
|
|
30
|
|
|
|
|
|
|
|
30
|
|
|
|
|
|
|
|
|
|
|
|
30
|
|
Accumulated deficit
|
|
|
(989,246
|
)
|
|
|
271,268
|
L
|
|
|
(717,978
|
)
|
|
|
120,734
|
L
|
|
|
86
|
L
|
|
|
(597,158
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(237,591
|
)
|
|
|
271,268
|
|
|
|
33,677
|
|
|
|
120,734
|
|
|
|
86
|
|
|
|
154,497
|
|
Treasury stock at cost,
73,842 shares
|
|
|
(911
|
)
|
|
|
|
|
|
|
(911
|
)
|
|
|
|
|
|
|
|
|
|
|
(911
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total stockholders equity
(deficit)
|
|
|
(238,502
|
)
|
|
|
271,268
|
|
|
|
32,766
|
|
|
|
120,734
|
|
|
|
86
|
|
|
|
153,586
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
285,932
|
|
|
$
|
(45,422
|
)
|
|
$
|
240,510
|
|
|
$
|
114,835
|
|
|
$
|
20,188
|
|
|
$
|
375,533
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
See accompanying notes to the Unaudited Pro Forma Condensed
Consolidated Financial Statements.
40
LIGAND
PHARMACEUTICALS INCORPORATED
Unaudited
Pro Forma Condensed Consolidated Statement of Operations
For
the Six Months Ended June 30, 2006
(In thousands except share data)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pro Forma
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
After
|
|
|
|
|
|
|
|
|
|
|
|
|
As
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Other
|
|
|
Pro Forma
|
|
|
|
Reported
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
as Adjusted
|
|
|
Revenues:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product sales
|
|
$
|
95,311
|
|
|
$
|
(66,146
|
)M
|
|
$
|
29,165
|
|
|
$
|
(29,165
|
)N
|
|
$
|
|
|
|
$
|
|
|
Collaborative research and
development and other revenues
|
|
|
4,092
|
|
|
|
|
|
|
|
4,092
|
|
|
|
(113
|
)N
|
|
|
|
|
|
|
3,979
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
|
99,403
|
|
|
|
(66,146
|
)
|
|
|
33,257
|
|
|
|
(29,278
|
)
|
|
|
|
|
|
|
3,979
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating costs and expenses:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of products sold
|
|
|
20,006
|
|
|
|
(10,968
|
)M
|
|
|
9,038
|
|
|
|
(9,038
|
)N
|
|
|
|
|
|
|
|
|
Research and development
|
|
|
26,113
|
|
|
|
(40
|
)M
|
|
|
26,073
|
|
|
|
(7,568
|
)N
|
|
|
(323
|
)P
|
|
|
19,652
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1,470
|
Q
|
|
|
|
|
Selling, general and administrative
|
|
|
46,988
|
|
|
|
(20,148
|
)M
|
|
|
26,840
|
|
|
|
(8,966
|
)N
|
|
|
(149
|
)P
|
|
|
18,327
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
602
|
Q
|
|
|
|
|
Accretion of deferred gain on sale
leaseback
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(982
|
)R
|
|
|
(982
|
)
|
Co-promotion
|
|
|
21,880
|
|
|
|
(21,880
|
)M
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Co-promote termination charges
|
|
|
132,507
|
|
|
|
(132,507
|
)M
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating costs and expenses
|
|
|
247,494
|
|
|
|
(185,543
|
)
|
|
|
61,951
|
|
|
|
(25,572
|
)
|
|
|
618
|
|
|
|
36,997
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations
|
|
|
(148,091
|
)
|
|
|
119,397
|
|
|
|
(28,694
|
)
|
|
|
(3,706
|
)
|
|
|
(618
|
)
|
|
|
(33,018
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income (expense):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income
|
|
|
1,160
|
|
|
|
|
|
|
|
1,160
|
|
|
|
|
|
|
|
|
|
|
|
1,160
|
|
Interest expense
|
|
|
(12,223
|
)
|
|
|
7,113
|
M
|
|
|
(616
|
)
|
|
|
50
|
N
|
|
|
425
|
P
|
|
|
(141
|
)
|
|
|
|
|
|
|
|
4,494
|
O
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other, net
|
|
|
1,002
|
|
|
|
|
|
|
|
1,002
|
|
|
|
|
|
|
|
|
|
|
|
1,002
|
|
Total other income (expense), net
|
|
|
(10,061
|
)
|
|
|
11,607
|
|
|
|
1,546
|
|
|
|
50
|
|
|
|
425
|
|
|
|
2,021
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss before income taxes
|
|
|
(158,152
|
)
|
|
|
131,004
|
|
|
|
(27,148
|
)
|
|
|
(3,656
|
)
|
|
|
(193
|
)
|
|
|
(30,997
|
)
|
Income tax expense
|
|
|
(35
|
)
|
|
|
|
|
|
|
(35
|
)
|
|
|
35
|
N
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1,464
|
N
|
|
|
(1,464
|
)N
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss
|
|
$
|
(158,187
|
)
|
|
$
|
131,004
|
|
|
$
|
(27,183
|
)
|
|
$
|
(2,157
|
)
|
|
$
|
(1,657
|
)
|
|
$
|
(30,997
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted per share amounts:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss
|
|
$
|
(2.03
|
)
|
|
|
|
|
|
$
|
(0.35
|
)
|
|
|
|
|
|
|
|
|
|
$
|
(0.40
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common
shares
|
|
|
78,021,236
|
|
|
|
|
|
|
|
78,021,236
|
|
|
|
|
|
|
|
|
|
|
|
78,021,236
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
See accompanying notes to the Unaudited Pro Forma Condensed
Consolidated Financial Statements.
41
LIGAND
PHARMACEUTICALS INCORPORATED
Unaudited
Pro Forma Condensed Consolidated Statement of Operations
For
the Year Ended December 31, 2005
(In thousands except share data)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pro Forma
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other
|
|
|
After
|
|
|
|
|
|
|
|
|
|
|
|
|
As
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Other
|
|
|
Pro Forma
|
|
|
|
Reported
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
as Adjusted
|
|
|
Revenues:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product sales
|
|
$
|
166,081
|
|
|
$
|
(112,793
|
)M
|
|
$
|
|
|
|
$
|
53,288
|
|
|
$
|
(53,288
|
)N
|
|
$
|
|
|
|
$
|
|
|
Collaborative research and
development and other revenues
|
|
|
10,527
|
|
|
|
|
|
|
|
|
|
|
|
10,527
|
|
|
|
(310
|
)N
|
|
|
|
|
|
|
10,217
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
|
176,608
|
|
|
|
(112,793
|
)
|
|
|
|
|
|
|
63,815
|
|
|
|
(53,598
|
)
|
|
|
|
|
|
|
10,217
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating costs and expenses:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of products sold
|
|
|
39,847
|
|
|
|
(23,090
|
)M
|
|
|
|
|
|
|
16,757
|
|
|
|
(16,757
|
)N
|
|
|
|
|
|
|
|
|
Research and development
|
|
|
56,075
|
|
|
|
(2,386
|
)M
|
|
|
|
|
|
|
53,689
|
|
|
|
(22,979
|
)N
|
|
|
(675
|
)P
|
|
|
33,130
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
3,095
|
Q
|
|
|
|
|
Selling, general and administrative
|
|
|
74,656
|
|
|
|
(33,034
|
)M
|
|
|
|
|
|
|
41,622
|
|
|
|
(18,488
|
)N
|
|
|
(261
|
)P
|
|
|
23,925
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1,052
|
Q
|
|
|
|
|
Accretion of deferred gain on sale
leaseback
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1,964
|
)R
|
|
|
(1,964
|
)
|
Co-promotion
|
|
|
32,501
|
|
|
|
(32,501
|
)M
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating costs and expenses
|
|
|
203,079
|
|
|
|
(91,011
|
)
|
|
|
|
|
|
|
112,068
|
|
|
|
(58,224
|
)
|
|
|
1,247
|
|
|
|
55,091
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations
|
|
|
(26,471
|
)
|
|
|
(21,782
|
)
|
|
|
|
|
|
|
(48,253
|
)
|
|
|
4,626
|
|
|
|
(1,247
|
)
|
|
|
(44,874
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income (expense):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income
|
|
|
1,890
|
|
|
|
|
|
|
|
|
|
|
|
1,890
|
|
|
|
|
|
|
|
|
|
|
|
1,890
|
|
Interest expense
|
|
|
(12,458
|
)
|
|
|
551
|
M
|
|
|
|
|
|
|
(1,550
|
)
|
|
|
244
|
N
|
|
|
871
|
P
|
|
|
(435
|
)
|
|
|
|
|
|
|
|
10,357
|
O
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other, net
|
|
|
699
|
|
|
|
|
|
|
|
|
|
|
|
699
|
|
|
|
|
|
|
|
|
|
|
|
699
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total other income (expense), net
|
|
|
(9,869
|
)
|
|
|
10,908
|
|
|
|
|
|
|
|
1,039
|
|
|
|
244
|
|
|
|
871
|
|
|
|
2,154
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss before income taxes
|
|
|
(36,340
|
)
|
|
|
(10,874
|
)
|
|
|
|
|
|
|
(47,214
|
)
|
|
|
4,870
|
|
|
|
(376
|
)
|
|
|
(42,720
|
)
|
Income tax expense
|
|
|
(59
|
)
|
|
|
4,354
|
|
|
|
(4,354
|
)M
|
|
|
(59
|
)
|
|
|
59
|
N
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss
|
|
$
|
(36,399
|
)
|
|
$
|
(6,520
|
)
|
|
$
|
(4,354
|
)
|
|
$
|
(47,273
|
)
|
|
$
|
4,929
|
|
|
$
|
(376
|
)
|
|
$
|
(42,720
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted per share amounts:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss
|
|
$
|
(0.49
|
)
|
|
|
|
|
|
|
|
|
|
$
|
(0.64
|
)
|
|
|
|
|
|
|
|
|
|
$
|
(0.58
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common
shares
|
|
|
74,019,501
|
|
|
|
|
|
|
|
|
|
|
|
74,019,501
|
|
|
|
|
|
|
|
|
|
|
|
74,019,501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
See accompanying notes to the Unaudited Pro Forma Condensed
Consolidated Financial Statements.
42
LIGAND
PHARMACEUTICALS INCORPORATED
Unaudited
Pro Forma Condensed Consolidated Statement of Operations
For
the Year Ended December 31, 2004
(In thousands except share data)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pro Forma
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
After
|
|
|
|
|
|
|
|
|
|
As
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Pro Forma
|
|
|
|
Reported
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
as Adjusted
|
|
|
Revenues:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product sales
|
|
$
|
120,335
|
|
|
$
|
(69,470
|
)M
|
|
$
|
50,865
|
|
|
$
|
(50,865
|
)N
|
|
$
|
|
|
Sale of royalty rights, net
|
|
|
31,342
|
|
|
|
|
|
|
|
31,342
|
|
|
|
|
|
|
|
31,342
|
|
Collaborative research and
development and other revenues
|
|
|
11,835
|
|
|
|
|
|
|
|
11,835
|
|
|
|
(535
|
)N
|
|
|
11,300
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
|
163,512
|
|
|
|
(69,470
|
)
|
|
|
94,042
|
|
|
|
(51,400
|
)
|
|
|
42,642
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating costs and expenses:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of products sold
|
|
|
39,804
|
|
|
|
(18,264
|
)M
|
|
|
21,540
|
|
|
|
(21,540
|
)N
|
|
|
|
|
Research and development
|
|
|
65,204
|
|
|
|
(1,978
|
)M
|
|
|
63,226
|
|
|
|
(32,484
|
)N
|
|
|
30,742
|
|
Selling, general and administrative
|
|
|
65,798
|
|
|
|
(33,851
|
)M
|
|
|
31,947
|
|
|
|
(19,367
|
)N
|
|
|
12,580
|
|
Co-promotion
|
|
|
30,077
|
|
|
|
(30,077
|
)M
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating costs and expenses
|
|
|
200,883
|
|
|
|
(84,170
|
)
|
|
|
116,713
|
|
|
|
(73,391
|
)
|
|
|
43,322
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations
|
|
|
(37,371
|
)
|
|
|
14,700
|
|
|
|
(22,671
|
)
|
|
|
21,991
|
|
|
|
(680
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income (expense):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income
|
|
|
1,096
|
|
|
|
|
|
|
|
1,096
|
|
|
|
|
|
|
|
1,096
|
|
Interest expense
|
|
|
(12,338
|
)
|
|
|
459
|
M
|
|
|
(1,590
|
)
|
|
|
332
|
N
|
|
|
(1,258
|
)
|
|
|
|
|
|
|
|
10,289
|
O
|
|
|
|
|
|
|
|
|
|
|
|
|
Other, net
|
|
|
3,705
|
|
|
|
|
|
|
|
3,705
|
|
|
|
|
|
|
|
3,705
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total other income (expense), net
|
|
|
(7,537
|
)
|
|
|
10,748
|
|
|
|
3,211
|
|
|
|
332
|
|
|
|
3,543
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Income (loss) before income taxes
|
|
|
(44,908
|
)
|
|
|
25,448
|
|
|
|
(19,460
|
)
|
|
|
22,323
|
N
|
|
|
2,863
|
|
Income tax expense
|
|
|
(233
|
)
|
|
|
|
|
|
|
(233
|
)
|
|
|
54
|
N
|
|
|
(179
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net Income (loss)
|
|
$
|
(45,141
|
)
|
|
$
|
25,448
|
|
|
$
|
(19,693
|
)
|
|
$
|
22,377
|
|
|
$
|
2,684
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic per share amounts:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income (loss)
|
|
$
|
(0.61
|
)
|
|
|
|
|
|
$
|
(0.27
|
)
|
|
|
|
|
|
$
|
0.04
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Diluted per share amounts:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income (loss)
|
|
$
|
(0.61
|
)
|
|
|
|
|
|
$
|
(0.27
|
)
|
|
|
|
|
|
$
|
0.04
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common
shares used in basic calculation
|
|
|
73,692,987
|
|
|
|
|
|
|
|
73,692,987
|
|
|
|
|
|
|
|
73,692,987
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common
shares used in diluted calculation
|
|
|
73,692,987
|
|
|
|
|
|
|
|
73,692,987
|
|
|
|
|
|
|
|
75,253,038
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
See accompanying notes to the Unaudited Pro Forma Condensed
Consolidated Financial Statements.
43
LIGAND
PHARMACEUTICALS INCORPORATED
Unaudited Pro Forma
Condensed Consolidated Statement of Operations
For the Year Ended December 31, 2003
(In
thousands, except share data)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pro Forma
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
After
|
|
|
|
|
|
|
|
|
|
As
|
|
|
AVINZA
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Pro Forma
|
|
|
|
Reported
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
Adjustments
|
|
|
as Adjusted
|
|
|
Revenues:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product sales
|
|
$
|
55,324
|
|
|
$
|
(16,482
|
)M
|
|
$
|
38,842
|
|
|
$
|
(38,842
|
)N
|
|
$
|
|
|
Sale of royalty rights, net
|
|
|
11,786
|
|
|
|
|
|
|
|
11,786
|
|
|
|
|
|
|
|
11,786
|
|
Collaborative research and
development and other revenues
|
|
|
14,008
|
|
|
|
|
|
|
|
14,008
|
|
|
|
(310
|
)N
|
|
|
13,698
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total revenues
|
|
|
81,118
|
|
|
|
(16,482
|
)
|
|
|
64,636
|
|
|
|
(39,152
|
)
|
|
|
25,484
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating costs and expenses:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of products sold
|
|
|
26,557
|
|
|
|
(12,383
|
)M
|
|
|
14,174
|
|
|
|
(14,174
|
)N
|
|
|
|
|
Research and development
|
|
|
66,678
|
|
|
|
(1,347
|
)M
|
|
|
65,331
|
|
|
|
(37,029
|
)N
|
|
|
28,302
|
|
Selling, general and administrative
|
|
|
52,540
|
|
|
|
(22,717
|
)M
|
|
|
29,823
|
|
|
|
(17,764
|
)N
|
|
|
12,059
|
|
Co-promotion
|
|
|
9,360
|
|
|
|
(9,360
|
)M
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating costs and expenses
|
|
|
155,135
|
|
|
|
(45,807
|
)
|
|
|
109,328
|
|
|
|
(68,967
|
)
|
|
|
40,361
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations
|
|
|
(74,017
|
)
|
|
|
29,325
|
|
|
|
(44,692
|
)
|
|
|
29,815
|
|
|
|
(14,877
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other income (expense):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income
|
|
|
783
|
|
|
|
|
|
|
|
783
|
|
|
|
|
|
|
|
783
|
|
Interest expense
|
|
|
(11,142
|
)
|
|
|
358
|
M
|
|
|
(559
|
)
|
|
|
121
|
N
|
|
|
(438
|
)
|
|
|
|
|
|
|
|
10,225
|
O
|
|
|
|
|
|
|
|
|
|
|
|
|
Other, net
|
|
|
(10,034
|
)
|
|
|
|
|
|
|
(10,034
|
)
|
|
|
|
|
|
|
(10,034
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total other income (expense), net
|
|
|
(20,393
|
)
|
|
|
10,583
|
|
|
|
(9,810
|
)
|
|
|
121
|
|
|
|
(9,689
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss before income taxes and
cumulative effect of a change in accounting principle
|
|
|
(94,410
|
)
|
|
|
39,908
|
|
|
|
(54,502
|
)
|
|
|
29,936
|
|
|
|
(24,566
|
)
|
Income tax expense
|
|
|
(56
|
)
|
|
|
|
|
|
|
(56
|
)
|
|
|
56
|
N
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from continuing operations
|
|
$
|
(94,466
|
)
|
|
$
|
39,908
|
|
|
$
|
(54,558
|
)
|
|
$
|
29,992
|
|
|
$
|
(24,566
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted per share
amounts:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss from continuing operations
|
|
$
|
(1.34
|
)
|
|
|
|
|
|
$
|
(0.77
|
)
|
|
|
|
|
|
$
|
(0.35
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted average number of common
shares
|
|
|
70,685,234
|
|
|
|
|
|
|
|
70,685,234
|
|
|
|
|
|
|
|
70,685,234
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
See accompanying notes to the Unaudited Pro Forma Condensed
Consolidated Financial Statements.
44
Basis
of Pro Forma Presentation
On September 6, 2006, the Company, King Pharmaceuticals,
Inc., a Tennessee corporation, and King Pharmaceuticals Research
and Development, Inc., a Delaware corporation and wholly-owned
subsidiary of King Pharmaceuticals (together with King
Pharmaceuticals, King) entered into a purchase
agreement (the AVINZA Purchase Agreement), pursuant
to which King agreed to acquire all of the Companys rights
in and to
AVINZA®
(morphine sulfate extended-release capsules) in the United
States, its territories and Canada, including, among other
things, all
Avinza®
inventory, equipment, records and related intellectual property,
and assume certain liabilities (together, AVINZA or
the AVINZA Product Line) as set forth in the AVINZA
Purchase Agreement. Additionally, a condition of the AVINZA
Purchase Agreement requires that the Company redeem, prior to
the close of the sale of AVINZA to King, the outstanding
6% convertible subordinated notes, previously issued by the
Company (the Debt Redemption). Also, King will
assume certain liabilities, including certain product-related
liabilities owed by the Company to Organon Pharmaceuticals USA
Inc. Pursuant to the AVINZA Purchase Agreement, at closing, the
Company will be paid a $265.0 million cash payment,
$15.0 million of which will be funded into an escrow
account to support any indemnification claims. The Company
expects to account for the disposition of the AVINZA Product
Line as a discontinued operation in its consolidated financial
statements.
Also on September 7, 2006, the Company, Eisai Inc., a
Delaware corporation and Eisai Co., Ltd., a Japanese company
(together with Eisai Inc., Eisai), entered into a
purchase agreement (the Oncology Purchase Agreement)
pursuant to which Eisai has agreed to acquire all of the
Companys worldwide rights in and to the Companys
oncology product line, including, among other things, all
related inventory, equipment, records and intellectual property,
and assume certain liabilities (together Oncology or
the Oncology Product Line) as set forth in the
Oncology Purchase Agreement. The Oncology Product Line includes
the Companys four marketed oncology drugs: ONTAK,
Targretin capsules, Targretin gel and Panretin gel. Pursuant to
the Oncology Purchase Agreement, at closing, the Company will be
paid a $205.0 million cash payment, $20.0 million of
which will be funded into an escrow account to support any
indemnification claims. The Company expects to account for the
disposition of the Oncology Product Line as a discontinued
operation in its consolidated financial statements.
On October 25, 2006, the Company entered into an agreement
with Slough Estates USA, Inc. (the Buyer) to sell
the real properties at its corporate headquarters located in
San Diego, California (the Sale Leaseback).
Under the terms of the agreement, Slough Estates USA, Inc. has
agreed to purchase all real properties (land, building and
improvements) known as 10275 Science Center Drive, 10265 Science
Center Drive and 10285 Science Center Drive in San Diego,
California for a purchase price of approximately
$47.6 million. In addition, the Company is leasing back the
building at10275 Science Center Drive from the Buyer as its
corporate headquarters office, with a lease term of fifteen
years through 2021. Under the terms of the lease, the Company
will pay a basic annual rent of approximately $3.0 million,
which is subject to an annual fixed percentage increase, and
management fees, property taxes and other necessary expenses
associated with the lease. Concurrent with the sale, the Company
will pay off its outstanding mortgage for the property. The
transaction is expected to close on or before November 27,
2006.
Together, the sale of AVINZA, the sale of Oncology, the Debt
Redemption and the Sale Leaseback are referred to as the
Transactions. The unaudited pro forma condensed
consolidated balance sheet as of June 30, 2006 gives effect
to the Transactions as if they occurred as of that date. The
unaudited pro forma condensed consolidated statements of
operations give effect to the Sale Leaseback as if it occurred
on January 1, 2005 and give effect to the sales of AVINZA
and Oncology as if they occurred on January 1, 2003, as
they are expected to be reported as discontinued operations in
the Companys consolidated financial statements. The Sale
Leaseback has not been reflected in the unaudited pro forma
condensed consolidated statements of operations for the years
ended December 31, 2004 and 2003, as it is not expected to
be reported as a discontinued operation in the Companys
consolidated financial statements. The unaudited pro forma
condensed consolidated financial statements have been derived
from, and should be read, in conjunction with the historical
consolidated financial statements, including the notes thereto,
in the Companys Annual Report filed on
Form 10-K
for the year ended December 31, 2005 and the Companys
Quarterly Report filed on
Form 10-Q
for the quarter ended June 30, 2006. The unaudited pro
forma condensed consolidated financial statements are not
necessarily indicative of the financial position or results of
operations of the Company that would have been achieved had the
Transactions described above occurred on the dates indicated or
that may be expected to occur as a result of such Transactions.
45
The unaudited pro forma condensed consolidated balance sheet
reflects significant assets and liabilities associated with the
AVINZA and Oncology Product Lines that will remain for a period
of time with the Company subsequent to the proposed
dispositions. Accordingly, the unaudited pro forma condensed
consolidated balance sheet may not reflect the ongoing financial
position of the Company. The unaudited pro forma condensed
consolidated statements of operations exclude revenues and
expenses directly attributable to AVINZA and Oncology, the Debt
Redemption and the Sale Leaseback. As such, the unaudited pro
forma condensed consolidated statements of operations do not
reflect a reduction of general corporate allocations or other
non-direct costs which may be expected to occur as a result of
the Transactions.
The Board of Directors of the Company is evaluating the
distribution of a substantial portion of the net cash proceeds
from the asset sales to the Companys shareholders in the
form of a special dividend following the consummation of the
Transactions. Additionally, the Company is seeking shareholder
approval to modify its 2002 Stock Incentive Plan (the 2002
Plan) to allow equitable adjustments to be made to options
outstanding under the 2002 Plan in the event of a special cash
dividend. Assuming shareholder approval of the change to the
2002 Plan, any such adjustments to outstanding options would be
considered a modification and result in the recognition of
compensation expense in the Companys consolidated
statement of operations under the requirements of Statement of
Financial Accounting Standard No 123(R) Share-Based
Payment (SFAS 123(R)). Any such expense
could be material. The accompanying unaudited pro forma
condensed consolidated financial statements do not reflect
adjustments related to the potential special cash dividend or
modifications to the terms of outstanding stock options that may
occur in connection with such a dividend.
Notes
to Unaudited Pro Forma Condensed Consolidated Financial
Statements
|
|
A. |
Reflects the adjustments to the Companys historical
consolidated balance sheet for the specific assets and
liabilities to be transferred to King under the AVINZA Purchase
Agreement.
|
|
|
B. |
Reflects the adjustments to the Companys historical
consolidated balance sheet for the specific assets and
liabilities to be transferred to Eisai under the Oncology
Purchase Agreement.
|
|
|
C. |
Reflects the adjustments to cash and cash equivalents related to
the sales of the AVINZA and Oncology product lines and the Debt
Redemption as follows:
|
The amounts in thousands:
|
|
|
|
|
|
|
|
|
|
|
AVINZA
|
|
|
Oncology
|
|
|
Cash consideration
|
|
$
|
265,000
|
|
|
$
|
205,000
|
|
Additional consideration to settle
product-line liabilities
|
|
|
10,000
|
|
|
|
|
|
Less: Cash held in escrow
|
|
|
(15,000
|
)
|
|
|
(20,000
|
)
|
Inventory value contingency
|
|
|
(65,341
|
)
|
|
|
|
|
Estimated transaction costs
|
|
|
(7,044
|
)
|
|
|
(2,710
|
)
|
Repayment of equipment financing
obligations for equipment transferred to King and Eisai
|
|
|
(502
|
)
|
|
|
(22
|
)
|
Redemption of 6% convertible
subordinated notes, including a contractual redemption premium
of $3,076
|
|
|
(131,226
|
)
|
|
|
|
|
Payment of accrued interest on
6% convertible subordinated notes
|
|
|
(961
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
54,926
|
|
|
$
|
182,268
|
|
|
|
|
|
|
|
|
|
|
As part of the Companys co-promotion termination agreement
with Organon, the Company agreed to pay Organon
$10.0 million in January 2007. In accordance with the
AVINZA Purchase Agreement, King is expected to reimburse Ligand
for this obligation. The AVINZA and Oncology Purchase Agreements
require a total of $35.0 million be held in escrow pending
the resolution of certain contingencies. Such amounts have been
excluded from the net sales consideration in the table above. If
these contingencies are resolved in favor of Ligand and
additional consideration is distributable, the additional
consideration received will serve to increase the Companys
gain on the disposal of the AVINZA and Oncology product lines.
46
Additionally, under the AVINZA Purchase Agreement, cash
consideration may be affected by an inventory value contingency
for product held in the distribution channel. Under this
arrangement, if the AVINZA inventory at closing is above an
agreed-upon level, the AVINZA purchase price will be adjusted
down. For purposes of the unaudited pro forma condensed
consolidated financial statements, the Company estimated the
potential reduction in cash consideration related to the
inventory value contingency based on inventory levels as of
June 30, 2006, and excluded such amounts from the net sales
consideration to be received. In the event that the inventory
value contingency resolves in an amount different than the
adjustment assumed in the unaudited pro forma condensed
consolidated financial statements, the purchase price will be
adjusted accordingly. Although the Company expects that the
adjustment may be significantly lower than that assumed in the
accompanying unaudited pro forma condensed consolidated balance
sheet due to lower current inventory levels, there can be no
assurance that the lower inventory levels will be sustained.
As of the closing date of the Oncology transaction, the Company
is required to transfer manufactured product inventory to Eisai
of at least $9.8 million (the Required Closing Date
Inventory Value). To the extent the actual inventory value
is less than the Required Closing Date Inventory Value, the
Oncology Purchase Agreement provides for a corresponding
decrease to the purchase price. As of June 30, 2006,
Oncology inventory exceeded $9.8 million. Furthermore, the
Company believes that Oncology inventory exceeded
$9.8 million on October 25, 2006, the date the sale of
Oncology was consummated. Accordingly, no such adjustment has
been reflected in the accompanying unaudited pro forma condensed
consolidated balance sheet. However, there can be no assurance
that the actual inventory value as of the Oncology closing date
did exceed the Required Closing Date Inventory, until final
approval from Eisai is obtained.
|
|
D. |
Reflects the removal of deferred revenue, deferred cost of
products sold and deferred royalty cost related to AVINZA and
Oncology due to the Transactions.
|
The Company accounts for domestic product shipments made to
wholesalers for AVINZA and Oncology under the sell-through
revenue recognition method. For these product sales, the Company
records deferred revenue and classifies inventory held by the
wholesaler as deferred cost of products sold within other
current assets. The Company recognizes revenue when such
inventory is sold through to the wholesalers customers
(Oncology) or when a prescription is filled (AVINZA).
Consequently, royalty cost associated with these product sales
is also deferred until the product revenue is recognized. Upon
closing of the AVINZA and Oncology transactions, the deferred
revenue, deferred cost of products sold, and the deferred
royalty cost associated with these product sales will be removed
from Ligands balance sheet and recognized as part of the
gain on the disposals of AVINZA and Oncology.
|
|
E. |
Reflects the write-off of debt issuance costs associated with
the redemption of the 6% convertible subordinated notes
(see Note I below).
|
|
|
F. |
Reflects adjustments to accrued liabilities related to the
Transactions for royalty payments, rebates and chargebacks.
|
The Company records accruals for royalty payments, rebates and
chargebacks when product sales are recognized as revenue under
the sell-through method. In connection with eliminating the
deferred revenue balances associated with AVINZA and Oncology
upon disposition (see note D above), the Company will
accrue for royalty payments, rebates and chargebacks, related to
product in the distribution channel which has not sold-through
and for which the Company will retain the liability subsequent
to the disposal of AVINZA and Oncology.
|
|
G. |
Reflects adjustments to record an estimate of product in the
wholesale and retail distribution channels that could be
returned based on estimated channel inventories as of
June 30, 2006. Based on the terms of the AVINZA and
Oncology transactions, the Company is required to retain the
obligation for returns for product shipped to wholesalers prior
to the closing of the transactions. As further discussed under
Note C, the Company expects product inventories in the
distribution channels at the time of close of each transaction
to be significantly lower than the levels estimated as of
June 30, 2006.
|
However, there can be no assurance that any such decrease in
inventories will be achieved or result in a lower estimate of
product returns.
47
|
|
H. |
Reflects the repayment of equipment financing obligations
related to equipment to be transferred to King and Eisai as a
result of the Transactions.
|
|
|
I. |
Reflects the redemption of the 6% convertible subordinated
notes as required by the AVINZA Purchase Agreement.
|
Though the AVINZA Purchase Agreement requires redemption of the
6% subordinated notes, note holders have the option to convert
the notes to Ligand common stock prior to redemption at a rate
of 161.9905 shares of common stock per $1,000 principal
amount of securities (effective conversion price of
approximately $6.17 per share of common stock). If a
portion or all of the notes are converted to equity instruments
rather than redeemed, the pro forma cash balances would increase
by an amount up to $132.2 million, reflecting the principal
amount of the notes, accrued interest and the redemption
premium. However, there can be no assurance that any or all of
the note holders will convert prior to redemption or the amount
by which cash balances may be adjusted.
|
|
J. |
Reflects the sale and subsequent leaseback of the Companys
corporate office building and land in San Diego, California
(the Sale Leaseback).
|
On October 25, 2006, the Company entered into a purchase
agreement with Slough Estates USA Inc. (the Buyer)
to sell the facilities encompassing the Companys corporate
headquarters and two land parcels. The total purchase price for
the facilities and land was approximately $47.6 million. As
a term of the purchase agreement, the Company will pay off the
outstanding bank loan on the building, the balance of which
approximated $11.7 million as of June 30, 2006. A
prepayment penalty approximating $0.4 million is expected
to be incurred (see Note L). Concurrently, the Company
entered into a lease agreement (the Lease) with the
Buyer dated October 25, 2006 to leaseback the office
building housing the Companys corporate headquarters. The
lease has a term of 15 years with a basic annual rent,
subject to an annual fixed percentage increase. The Sale
Leaseback transaction will be recorded per Statement of
Financial Accounting Standard No. 13 Accounting for
Leases. The Company expects to record an immediate gain on
the sale totalling approximately $2.8 million and defer a
gain of approximately $29.5 million on the sale of the
corporate headquarters, which will be recognized on a
straight-line basis over the
15-year life
of the lease at a rate of approximately $2.0 million per
year.
|
|
K. |
Reflects current tax liabilities for federal Alternative Minimum
Tax (AMT) and certain state taxes associated with
the sales of AVINZA and Oncology and the Sale Leaseback, based
on the expected proceeds to be received in the current period.
Future royalties to be received from King on sales of AVINZA and
the release of escrow amounts for both the AVINZA and Oncology
sales transactions are expected to be taxable in the year
received by the Company. There can be no assurance of the extent
to which net operating loss carryforwards (NOLs) or
tax credits will be available to offset or otherwise minimize
any such taxable gains.
|
The estimated taxable gains on the dispositions of AVINZA and
Oncology and the Sale Leaseback have been reduced, fully for
federal purposes and partially for state purposes, by the
estimated utilization of NOLs, which the Company has estimated
to be available. However, the Company has not completed its
analysis of the tax implications of the Transactions.
Accordingly, the Companys ability to utilize its NOLs and
research and development credit carryforwards (R&D
Credits) for State of California purposes may materially
differ from the amounts assumed to be used in the unaudited pro
forma condensed consolidated financial statements. In particular:
|
|
|
|
|
The Companys expectation of federal tax to the extent of
AMT is predicated upon the full value of the NOLs being
available, which in turn is predicated on certain assumptions
regarding the valuation of the Companys intellectual
property on the date of the Transactions and the dates of prior
ownership changes and certain tax elections and options which
may be available to the Company. Changes to the valuations of
intellectual property could result in material limitations on
the Companys ability to fully utilize such NOLs.
|
|
|
|
The Company has not completed its study of the availability of
R&D Credits in the State of California. While the Company
believes it has sufficient R&D credits to offset some or all
of the taxable gains from the Transactions, it has assumed no
R&D Credit utilization in the unaudited pro forma condensed
consolidated
|
48
|
|
|
|
|
financial statements, as it can not yet determine a reasonable
estimate of the R&D Credits which ultimately may be
available.
|
Furthermore, the tax implications of the Transactions could be
affected by the ultimate decisions by the holders of the
6% subordinated notes to accept redemption of their notes
or to convert their notes to shares in the Companys stock.
For example, a conversion of notes could result in a change in
ownership which could in turn result in limitations on the
utilization of NOLs generated since the Company last determined
an ownership change in 2005. As described in Note I above,
the unaudited pro forma condensed consolidated financial
statements assume that the 6% subordinated notes will be fully
redeemed.
|
|
L. |
Reflects an estimated net gain, net of tax, on the sales of
AVINZA and Oncology, the Sale Leaseback, an estimated loss on
redemption of the 6% subordinated notes, and extinguishment of
the mortgage debt.
|
The amounts in thousands
Gain
on AVINZA Transaction
|
|
|
|
|
|
|
AVINZA
|
|
|
Adjusted cash consideration
|
|
$
|
187,615
|
|
Total assets transferred
|
|
|
(90,526
|
)
|
Total liabilities assumed
|
|
|
139,307
|
|
Other assets and liabilities
removed and created upon disposal
|
|
|
55,155
|
|
Debt
Redemption
|
|
|
|
|
Cash paid to redeem
6% subordinated notes
|
|
|
(132,187
|
)
|
Debt issuance cost write-off
|
|
|
(1,358
|
)
|
Carrying value of
6% subordinated notes
|
|
|
128,150
|
|
Accrued interest
|
|
|
961
|
|
|
|
|
|
|
Estimated gain on disposal of
AVINZA
|
|
|
287,117
|
|
Estimated tax on gain
|
|
|
(15,849
|
)
|
|
|
|
|
|
Estimated net gain from AVINZA
transaction
|
|
$
|
271,268
|
|
|
|
|
|
|
Gain
on Oncology Transaction
|
|
|
|
|
|
|
Oncology
|
|
|
Adjusted cash consideration
|
|
$
|
182,290
|
|
Total assets transferred
|
|
|
(65,813
|
)
|
Total liabilities assumed
|
|
|
584
|
|
Other assets and liabilities
removed and created upon disposal
|
|
|
10,778
|
|
Estimated tax on gain
|
|
|
(7,105
|
)
|
|
|
|
|
|
Estimated net gain from
Oncology transaction
|
|
$
|
120,734
|
|
|
|
|
|
|
49
Gain
on Sale Leaseback Transaction
|
|
|
|
|
Cash proceeds from Sale Leaseback,
net of transaction costs of $719
|
|
$
|
46,923
|
|
Carrying value of land sold
|
|
|
(5,176
|
)
|
Carrying value of building sold
|
|
|
(5,778
|
)
|
Carrying value of leasehold
improvements sold
|
|
|
(3,712
|
)
|
|
|
|
|
|
Total pre-tax gain on Sale
Leaseback
|
|
|
32,257
|
|
Less: current portion of pre-tax
deferred gain
|
|
|
1,964
|
|
Less: non-current portion of
pre-tax deferred gain
|
|
|
27,498
|
|
|
|
|
|
|
Pre-tax gain immediately
recognized on sale
|
|
|
2,795
|
|
Pre-tax loss on early
extinguishment of debt
|
|
|
(400
|
)
|
Estimated tax on gain
|
|
|
(2,309
|
)
|
|
|
|
|
|
Estimated net current gain from
Sale Leaseback Transaction
|
|
$
|
86
|
|
|
|
|
|
|
|
|
M. |
Reflects adjustments to remove the results of operations
directly attributable to the AVINZA Product Line. Income tax
expense has been computed using statutory rates on the pro forma
adjustments to the extent of Product Line income. However, since
the Company retains a full valuation allowance with respect to
its net deferred tax assets, an offsetting adjustment has been
reflected through other AVINZA adjustments. A non recurring net
gain on sale has been excluded from the unaudited pro forma
condensed consolidated statements of operations, but will be
included in the Companys consolidated statement of
operations when the sale of AVINZA is concluded.
|
|
|
N.
|
Reflects adjustments to remove the results of operations
directly attributable to the Oncology Product Line. Income tax
expense has been computed using statutory rates on the pro forma
adjustments to the extent of Product Line income. However, since
the Company retains a full valuation allowance with respect to
its net deferred tax assets, an offsetting adjustment has been
reflected through other adjustments. A non-recurring net gain on
sale has been excluded from the unaudited pro forma condensed
consolidated statements of operations, but will be included in
the Companys consolidated statement of operations when the
sale of Oncology is concluded.
|
|
O.
|
Reflects adjustments to remove interest expense and related
amortization of deferred debt costs attributable to the
6% convertible subordinated notes. A non-recurring loss of
$4.4 million associated with the Debt Redemption has been
excluded from the unaudited pro forma condensed consolidated
statements of operations, but will be included in the
Companys consolidated statement of operations if the debt
is fully redeemed rather than being converted to shares of the
Companys common stock at the time of such redemption.
|
|
|
P. |
Reflects adjustments to reverse historical expenses for
depreciation, mortgage interest and other operating expenses
recorded in the Companys historical consolidated financial
statements for the Companys corporate headquarters, which
was sold in the Sale Leaseback.
|
|
|
Q.
|
Reflects adjustments to record annual base rent expense of
$3.7 million and annual executory costs of
$0.4 million for the lease of the Companys corporate
headquarters entered into in connection with the Sale Leaseback.
These expenses have been allocated to research and development
expenses and selling, general, and administrative expenses in
the unaudited pro forma condensed consolidated statements of
operations using the Companys historical allocation
percentages.
|
|
R.
|
Reflects the accretion of the deferred gain resulting from the
Sale Leaseback over the 15- year term of the related lease.
|
50
UNAUDITED
FINANCIAL STATEMENTS OF AVINZA PRODUCT LINE OF LIGAND
PHARMACEUTICALS INCORPORATED
The following are unaudited financial statements of the AVINZA
product line of Ligand Pharmaceuticals Incorporated (the
Company or Ligand). These unaudited
financial statements have been derived from historical financial
data of Ligand Pharmaceuticals Incorporated and include
unaudited balance sheets of the AVINZA product line as of
June 30, 2006 and December 31, 2005 and 2004, and the
related unaudited statements of operations and cash flows for
the six months ended June 30, 2006 and 2005, and for each
of the years in the three year period ended December 31,
2005. These unaudited financial statements reflect the assets
and liabilities, operations and cash flows of the AVINZA product
line and include allocations for expenses incurred by Ligand on
behalf of the AVINZA product line. The unaudited financial
statements are not necessarily indicative of the financial
position, results of operations or cash flows that would have
occurred had the AVINZA product line been a stand-alone entity
during the periods presented, nor is it indicative of future
results of the AVINZA product line.
The unaudited financial statements of the AVINZA product line
are qualified in their entireties by, and should be read in
conjunction with, the audited historical consolidated financial
statements of Ligand Pharmaceuticals Incorporated including the
notes thereto, in the Companys Annual Report on
Form 10-K
for the year ended December 31, 2005, and the
Companys Quarterly Report on
Form 10-Q
for the quarter ended June 30, 2006, which are incorporated
by reference herein.
51
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
BALANCE SHEETS
(Unaudited)
(In thousands)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
ASSETS
|
|
|
|
|
|
|
|
|
|
|
|
|
Current assets
|
|
|
|
|
|
|
|
|
|
|
|
|
Accounts receivable, net
|
|
$
|
12,073
|
|
|
$
|
14,842
|
|
|
$
|
22,508
|
|
Inventories, net
|
|
|
2,922
|
|
|
|
2,870
|
|
|
|
3,742
|
|
Other current assets
|
|
|
9,175
|
|
|
|
10,017
|
|
|
|
8,786
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total current assets
|
|
|
24,170
|
|
|
|
27,729
|
|
|
|
35,036
|
|
Restricted investments
|
|
|
309
|
|
|
|
317
|
|
|
|
188
|
|
Equipment, net
|
|
|
765
|
|
|
|
849
|
|
|
|
937
|
|
Acquired technology and product
rights, net
|
|
|
86,897
|
|
|
|
90,712
|
|
|
|
98,341
|
|
Other assets
|
|
|
44
|
|
|
|
56
|
|
|
|
86
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total assets
|
|
$
|
112,185
|
|
|
$
|
119,663
|
|
|
$
|
134,588
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND NET PRODUCT
LINE DEFICIT
|
|
|
|
|
|
|
|
|
|
|
|
|
Current liabilities
|
|
|
|
|
|
|
|
|
|
|
|
|
Accounts payable
|
|
$
|
8,260
|
|
|
$
|
5,062
|
|
|
$
|
7,502
|
|
Accrued liabilities
|
|
|
29,970
|
|
|
|
41,931
|
|
|
|
24,627
|
|
Deferred revenue, net
|
|
|
107,537
|
|
|
|
115,235
|
|
|
|
102,765
|
|
Current portion of co-promote
termination liability
|
|
|
45,046
|
|
|
|
|
|
|
|
|
|
Current portion of equipment
financing obligations
|
|
|
274
|
|
|
|
270
|
|
|
|
273
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total current liabilities
|
|
|
191,087
|
|
|
|
162,498
|
|
|
|
135,167
|
|
Long-term portion of co-promote
termination liability
|
|
|
94,261
|
|
|
|
|
|
|
|
|
|
Long-term portion of equipment
financing obligations
|
|
|
284
|
|
|
|
406
|
|
|
|
642
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total liabilities
|
|
|
285,632
|
|
|
|
162,904
|
|
|
|
135,809
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Commitments and contingencies
|
|
|
|
|
|
|
|
|
|
|
|
|
Net product line deficit
|
|
|
(173,447
|
)
|
|
|
(43,241
|
)
|
|
|
(1,221
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total liabilities and net product
line deficit
|
|
$
|
112,185
|
|
|
$
|
119,663
|
|
|
$
|
134,588
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The accompanying notes are integral part of these unaudited
financial statements.
52
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
STATEMENTS OF OPERATIONS
(Unaudited)
(In thousands)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Six Months Ended June 30,
|
|
|
Years Ended December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Revenues:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product sales, net
|
|
$
|
66,146
|
|
|
$
|
49,458
|
|
|
$
|
112,793
|
|
|
$
|
69,470
|
|
|
$
|
16,482
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating costs and expenses:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of products sold
|
|
|
10,968
|
|
|
|
11,565
|
|
|
|
23,090
|
|
|
|
18,264
|
|
|
|
12,383
|
|
Research and development
|
|
|
173
|
|
|
|
600
|
|
|
|
2,972
|
|
|
|
2,567
|
|
|
|
1,417
|
|
Selling, general and administrative
|
|
|
27,552
|
|
|
|
22,745
|
|
|
|
42,476
|
|
|
|
38,331
|
|
|
|
26,094
|
|
Co-promotion
|
|
|
21,880
|
|
|
|
14,706
|
|
|
|
32,501
|
|
|
|
30,077
|
|
|
|
9,360
|
|
Co-promote termination charges
|
|
|
132,507
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating costs and expenses
|
|
|
193,080
|
|
|
|
49,616
|
|
|
|
101,039
|
|
|
|
89,239
|
|
|
|
49,254
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Income (loss) from operations
|
|
|
(126,934
|
)
|
|
|
(158
|
)
|
|
|
11,754
|
|
|
|
(19,769
|
)
|
|
|
(32,772
|
)
|
Interest expense
|
|
|
(7,115
|
)
|
|
|
(309
|
)
|
|
|
(558
|
)
|
|
|
(469
|
)
|
|
|
(370
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Income (loss) before income taxes
|
|
|
(134,049
|
)
|
|
|
(467
|
)
|
|
|
11,196
|
|
|
|
(20,238
|
)
|
|
|
(33,142
|
)
|
Income tax benefit (expense)
|
|
|
(2,149
|
)
|
|
|
501
|
|
|
|
(12,015
|
)
|
|
|
(8,952
|
)
|
|
|
(1,522
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income (loss)
|
|
$
|
(136,198
|
)
|
|
$
|
34
|
|
|
$
|
(819
|
)
|
|
$
|
(29,190
|
)
|
|
$
|
(34,664
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The accompanying notes are integral part of these unaudited
financial statements.
53
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
STATEMENTS OF CHANGES IN NET PRODUCT LINE EQUITY/(DEFICIT)
(Unaudited)
(In thousands)
|
|
|
|
|
|
Balance at December 31, 2002
|
|
$
|
99,417
|
|
Net loss
|
|
|
(34,664
|
)
|
Net distributions to Ligand
|
|
|
(18,822
|
)
|
|
|
|
|
|
Balance at December 31, 2003
|
|
|
45,931
|
|
Net loss
|
|
|
(29,190
|
)
|
Net distributions to Ligand
|
|
|
(17,962
|
)
|
|
|
|
|
|
Balance at December 31, 2004
|
|
|
(1,221
|
)
|
Net loss
|
|
|
(819
|
)
|
Net distributions to Ligand
|
|
|
(41,201
|
)
|
|
|
|
|
|
Balance at December 31, 2005
|
|
|
(43,241
|
)
|
Net loss
|
|
|
(136,198
|
)
|
Stock compensation expense
|
|
|
175
|
|
Net contributions from Ligand
|
|
|
5,817
|
|
|
|
|
|
|
Balance at June 30, 2006
|
|
$
|
(173,447
|
)
|
|
|
|
|
|
The accompanying notes are integral part of these unaudited
financial statements.
54
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
STATEMENTS OF CASH FLOWS
(Unaudited)
(In thousands)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Six Months Ended June 30,
|
|
|
Years Ended December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Operating activities
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net income (loss)
|
|
$
|
(136,198
|
)
|
|
$
|
34
|
|
|
$
|
(819
|
)
|
|
$
|
(29,190
|
)
|
|
$
|
(34,664
|
)
|
Adjustments to reconcile net
income (loss) to net cash provided by (used in) operating
activities:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Amortization of acquired
technology and product rights
|
|
|
3,815
|
|
|
|
3,814
|
|
|
|
7,629
|
|
|
|
7,629
|
|
|
|
7,644
|
|
Depreciation of equipment
|
|
|
176
|
|
|
|
180
|
|
|
|
358
|
|
|
|
300
|
|
|
|
226
|
|
Stock based compensation expense
|
|
|
175
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other
|
|
|
(8
|
)
|
|
|
(6
|
)
|
|
|
|
|
|
|
(5
|
)
|
|
|
6
|
|
Changes in current assets and
liabilities Accounts receivable, net
|
|
|
2,769
|
|
|
|
3,810
|
|
|
|
7,666
|
|
|
|
(10,427
|
)
|
|
|
(11,010
|
)
|
Inventories, net
|
|
|
(52
|
)
|
|
|
1,554
|
|
|
|
872
|
|
|
|
(3,162
|
)
|
|
|
696
|
|
Other current assets
|
|
|
842
|
|
|
|
1,034
|
|
|
|
(1,231
|
)
|
|
|
(3,610
|
)
|
|
|
(2,538
|
)
|
Accounts payable and accrued
liabilities
|
|
|
(8,764
|
)
|
|
|
(885
|
)
|
|
|
14,865
|
|
|
|
13,492
|
|
|
|
16,338
|
|
Deferred revenue, net
|
|
|
(7,698
|
)
|
|
|
6,078
|
|
|
|
12,470
|
|
|
|
42,511
|
|
|
|
47,402
|
|
Co-promote termination liability
|
|
|
139,307
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net cash provided by (used in)
operating activities
|
|
|
(5,636
|
)
|
|
|
15,613
|
|
|
|
41,810
|
|
|
|
17,538
|
|
|
|
24,100
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Investing activities
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Decrease (increase) in restricted
investments
|
|
|
9
|
|
|
|
(124
|
)
|
|
|
(129
|
)
|
|
|
(13
|
)
|
|
|
(124
|
)
|
Purchases of equipment
|
|
|
(92
|
)
|
|
|
(201
|
)
|
|
|
(270
|
)
|
|
|
(364
|
)
|
|
|
(1,058
|
)
|
Payment for
AVINZA®
royalty rights
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(4,133
|
)
|
Other, net
|
|
|
20
|
|
|
|
22
|
|
|
|
30
|
|
|
|
10
|
|
|
|
(31
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net cash used in investing
activities
|
|
|
(63
|
)
|
|
|
(303
|
)
|
|
|
(369
|
)
|
|
|
(367
|
)
|
|
|
(5,346
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Financing activities
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Principal payments on equipment
financing obligations
|
|
|
(149
|
)
|
|
|
(155
|
)
|
|
|
(333
|
)
|
|
|
(201
|
)
|
|
|
|
|
Proceeds from equipment financing
arrangements
|
|
|
31
|
|
|
|
71
|
|
|
|
93
|
|
|
|
992
|
|
|
|
68
|
|
Net contributions from
(distributions to) Ligand
|
|
|
5,817
|
|
|
|
(15,226
|
)
|
|
|
(41,201
|
)
|
|
|
(17,962
|
)
|
|
|
(18,822
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net cash provided by (used in)
financing activities
|
|
|
5,699
|
|
|
|
(15,310
|
)
|
|
|
(41,441
|
)
|
|
|
(17,171
|
)
|
|
|
(18,754
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net change in cash and cash
equivalents
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents,
beginning of period
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents, end of
period
|
|
$
|
|
|
|
$
|
|
|
|
$
|
|
|
|
$
|
|
|
|
$
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The accompanying notes are integral part of these unaudited
financial statements.
55
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS
(UNAUDITED)
|
|
Note 1:
|
Description
of Business and Basis of Presentation
|
The AVINZA product business (AVINZA or the
Business) is a product line of Ligand
Pharmaceuticals Incorporated (the Company or
Ligand). AVINZA was approved by the Food and Drug
Administration (FDA) in March 2002 for the once-daily
treatment of
moderate-to-severe
pain in patients who require continuous,
around-the-clock
opioid therapy for an extended period of time. Ligand launched
the product in the second quarter of 2002. AVINZA consists of
two components: an immediate-release component that rapidly
achieves morphine concentrations in plasma, and an
extended-release component that maintains plasma concentrations
throughout a
24-hour
dosing interval. AVINZA was developed by Elan Corporation, plc
(Elan), which licensed the U.S. and Canadian rights
to the Company in 1998. Early in 2003, Ligand finalized a
co-promotion agreement with Organon Pharmaceuticals USA Inc.
(Organon), which was subsequently terminated
effective January 1, 2006. However, the parties agreed to
continue to cooperate during a transition period ending
September 30, 2006 to promote the product. The AVINZA
financial statements include the unaudited financial position,
results of operations, and cash flows of the Business.
The unaudited financial statements have been carved out from the
consolidated financial statements of Ligand using the historical
assets and liabilities, results of operations and cash flows of
Ligand attributable to AVINZA. The carve out financial
statements include allocations for certain corporate expenses
incurred by Ligand on behalf of the Business. See Note 4,
Corporate Expense Allocations. Management believes
the assumptions underlying the unaudited carve-out financial
statements of AVINZA are reasonable; however, AVINZAs
financial position, results of operations, and cash flows may
have been materially different if it was operated as a
stand-alone entity as of and for the periods presented.
As a product line of Ligand, AVINZA is dependent upon Ligand for
all of its working capital and financing requirements.
Accordingly, the transfers of financial resources between Ligand
and the Business are reflected as a component of net product
line deficit in lieu of cash, intercompany debt, and equity
accounts.
|
|
Note 2:
|
Summary
of Significant Accounting Policies
|
Use of
Estimates
The preparation of financial statements in conformity with
generally accepted accounting principles requires the use of
estimates and assumptions that affect the reported amounts of
assets and liabilities, including disclosure of contingent
assets and contingent liabilities, at the date of the financial
statements and the reported amounts of revenues and expenses
during the reporting periods. The Business critical
accounting policies are those that are both most important to
the Business financial condition and results of operations
and require the most difficult, subjective or complex judgments
on the part of management in their application, often as a
result of the need to make estimates about the effect of matters
that are inherently uncertain.
Because of the uncertainty of factors surrounding the estimates
or judgments used in the preparation of the financial
statements, actual results may materially vary from these
estimates.
Restricted
Investments
Restricted investments consist of certificates of deposit
entered into by Ligand and attributable to AVINZA held with a
financial institution as collateral under a third-party service
provider arrangement. These certificates have been classified by
management as
held-to-maturity
and are accounted for at amortized cost.
Concentrations
of Credit Risk
Financial instruments that potentially subject the Business to
significant concentrations of credit risk consist primarily of
accounts receivable. The Business extends credit on an
uncollateralized basis primarily to wholesale
56
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
drug distributors throughout the United States. Prior to
entering into sales agreements with new customers, and on an
ongoing basis for existing customers, the Business performs
credit evaluations. To date, the Business has not experienced
significant losses on customer accounts.
As more fully discussed in Note 5, Ligand sells certain of
the Business accounts receivable under a non-recourse
factoring arrangement with a finance company. Ligand can
transfer funds in any amount up to a specified percentage of the
net amount due from the Business trade customers at the
time of the sale to the finance company, with the remaining
funds available upon collection of the trade receivable. As of
June 30, 2006, the gross amount due from the finance
company for the sale of AVINZA related receivables was
$9.2 million (see Note 3).
Inventories,
net
Inventories, net are stated at the lower of cost or market
value. Cost is determined using the
first-in-first-out
method. Inventories, net consist of the following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Work-in-process
|
|
$
|
760
|
|
|
$
|
554
|
|
|
$
|
|
|
Finished goods
|
|
|
2,162
|
|
|
|
2,601
|
|
|
|
3,742
|
|
Less inventory reserves
|
|
|
|
|
|
|
(285
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
2,922
|
|
|
$
|
2,870
|
|
|
$
|
3,742
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Equipment
Equipment is stated at cost and consists of the following (in
thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Equipment
|
|
$
|
1,217
|
|
|
$
|
1,250
|
|
|
$
|
1,203
|
|
Less accumulated depreciation
|
|
|
(452
|
)
|
|
|
(401
|
)
|
|
|
(266
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
765
|
|
|
$
|
849
|
|
|
$
|
937
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Depreciation of equipment is computed using the straight-line
method over the estimated useful lives of the assets which range
from three to ten years.
Acquired
Technology and Product Rights
In accordance with Statement of Financial Accounting Standard
(SFAS) No. 142, Goodwill and Other Intangibles
(SFAS 142), the Business amortizes
intangible assets with finite lives in a manner that reflects
the pattern in which the economic benefits of the assets are
consumed or otherwise used up. If that pattern cannot be
reliably determined, the assets are amortized using the
straight-line method. Acquired technology and product rights,
which are being amortized through November 2017, consist of the
following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
AVINZA
|
|
$
|
114,437
|
|
|
$
|
114,437
|
|
|
$
|
114,437
|
|
Less accumulated depreciation
|
|
|
(27,540
|
)
|
|
|
(23,725
|
)
|
|
|
(16,096
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
86,897
|
|
|
$
|
90,712
|
|
|
$
|
98,341
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Amortization of acquired technology and product rights for each
of the six months ended June 30, 2006 and 2005 was
$3.8 million and for each of the years ended
December 31, 2005, 2004 and 2003 was $7.6 million.
57
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Estimated annual amortization for these assets for each of the
years in the period from 2006 to 2010 is $7.6 million and
$52.7 million, thereafter.
Fair
Value of Financial Instruments
The carrying amounts of accounts receivable, restricted
investments, accounts payable and accrued liabilities at
June 30, 2006, December 31, 2005 and December 31,
2004 are considered to be reasonable estimates of their fair
values due to the short-term nature of those instruments. As of
June 30, 2006, December 31, 2005 and December 31,
2004, the carrying amounts of equipment financing obligations
represent reasonable estimates of their fair value due to their
interest rates approximating current market rates. The carrying
amount of the co-promotion termination liability is based upon
the present value of future cash payments expected to be made
under the arrangement, which is believed to represent fair value.
Revenue
Recognition
The Business has determined that shipments made to wholesalers
for AVINZA do not meet the revenue recognition criteria of
SFAS No. 48, Revenue Recognition When Right of
Return Exists (SFAS 48), and Staff
Accounting Bulletin (SAB) 104, Revenue
Recognition (SAB 104), at the time of
shipment, and therefore such shipments are accounted for using
the sell-through method. Under the sell-through method, the
Business does not recognize revenue upon shipment of product to
the wholesaler. For these product sales, the Business invoices
the wholesaler, records deferred revenue at gross invoice sales
price less estimated cash discounts and classifies the inventory
held by the wholesaler as deferred cost of goods
sold within other current assets. At that
point, the Business makes an estimate of units that may be
returned and records a reserve for those units against the
deferred cost of goods sold account. The Business
recognizes revenue when such inventory is sold through, on a
first-in,
first-out (FIFO) basis. Sell-through for AVINZA is considered to
be at the prescription level or at the point of patient
consumption for channels with no prescription requirements.
Additionally under the sell-through method, royalties paid based
on unit shipments to wholesalers are deferred and recognized as
royalty expense as those units are sold through and recognized
as revenue. Royalties paid to technology partners are deferred
as the Business has the right to offset royalties paid for
product that is later returned against subsequent royalty
obligations. Royalties for which the Business does not have the
ability to offset (for example, royalties at the end of the
contracted royalty period which are not refundable) are expensed
in the period the royalty obligation becomes due.
The Business estimates sell-through based upon (1) analysis
of third-party information, including information obtained from
certain wholesalers with respect to their inventory levels and
sell-through to customers, and third-party market research data,
and (2) the Business internal product movement
information. To assess the reasonableness of third-party demand
(i.e. sell-through) information, the Business prepares separate
demand reconciliations based on inventory in the distribution
channel. Differences identified through these reconciliations
outside an acceptable range will be recognized as an adjustment
to the third-party reported demand in the period those
differences are identified. This adjustment mechanism is
designed to identify and correct for any material variances
between reported and actual demand over time and other potential
anomalies such as inventory shrinkage at wholesalers. The
Business estimates are subject to the inherent limitations
of estimates that rely on third-party data, as certain
third-party information is itself in the form of estimates. The
Business sales and revenue recognition under the
sell-through method reflects the Business estimates of
actual product sold through the channel.
The Business uses information from external sources to estimate
its gross product sales under the sell-through revenue
recognition method and significant gross to net sales
adjustments. Such estimates include product information with
respect to prescriptions, wholesaler out-movement and inventory
levels, retail pharmacy stocking levels, and the Business
own internal information. The Business receives information from
IMS Health, a supplier of market research to the pharmaceutical
industry, which it uses to estimate sell-through demand for its
products and retail pharmacy inventory levels. The Business also
receives wholesaler out-movement and inventory information
58
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
from its wholesaler customers that is used to support and
validate its demand-based, sell-through revenue recognition
estimates. The inventory information received from wholesalers
is a product of their record-keeping process and their internal
controls surrounding such processes.
Net product sales represent total product sales less allowances
for rebates, chargebacks, discounts, promotions and losses to be
incurred on returns from wholesalers resulting from increases in
the selling price of the Business products. In addition,
the Business incurs certain distributor service agreement fees
related to the management of its product by wholesalers. These
fees have been recorded within net revenues.
Deferred
Revenue, Net
Under the sell-through revenue recognition method, the Business
does not recognize revenue upon shipment of product to the
wholesaler. For these shipments, the Business invoices the
wholesaler, records deferred revenue at gross invoice sales
price, and classifies the inventory held by the wholesaler and
subsequently held by retail pharmacies as deferred cost of
goods sold within other current assets.
Deferred revenue is presented net of deferred cash and other
discounts.
The composition of deferred revenue, net is as follows (in
thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Deferred product revenue
|
|
$
|
109,025
|
|
|
$
|
116,538
|
|
|
$
|
104,675
|
|
Deferred discounts
|
|
|
(1,488
|
)
|
|
|
(1,303
|
)
|
|
|
(1,910
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Deferred revenue, net(1)
|
|
$
|
107,537
|
|
|
$
|
115,235
|
|
|
$
|
102,765
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1) |
|
Deferred revenue does not include other gross to net revenue
adjustments made when the Business reports net product sales.
Such adjustments include Medicaid rebates, managed health care
rebates, and government chargebacks, which are included in
accrued liabilities in the accompanying consolidated financial
statements. |
Allowance
for Return Losses
Product sales are net of adjustments for losses resulting from
price increases the Business may experience on product returns
from its wholesaler customers. The Business policy for
returns of AVINZA allows customers to return the product six
months prior to and six months after expiration. Upon an
announced price increase, typically in the quarter prior to when
a price increase becomes effective, the Business revalues its
estimate of deferred product revenue to be returned to recognize
the potential higher credit a wholesaler may take upon product
return determined as the difference between the new price and
the previous price used to value the allowance.
Medicaid
Rebates
The Business products are subject to state
government-managed Medicaid programs whereby discounts and
rebates are provided to participating state governments.
Medicaid rebates are accounted for by establishing an accrual in
an amount equal to the Business estimate of Medicaid
rebate claims attributable to sales recognized in that period.
The estimate of the Medicaid rebates accrual is determined
primarily based on historical experience regarding Medicaid
rebates, as well as current and historical prescription activity
provided by external sources, current contract prices and any
expected contract changes. The Business additionally considers
any legal interpretations of the applicable laws related to
Medicaid and qualifying federal and state government programs
and any new information regarding changes in the Medicaid
programs regulations and guidelines that would impact the
amount of the rebates. The Business adjusts the accrual
periodically throughout each period to reflect actual
experience, expected changes in future prescription volumes and
any changes in business circumstances or trends.
59
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Government
Chargebacks
The Business products are subject to certain programs with
federal government entities and other parties whereby pricing on
products is extended below wholesaler list price to
participating entities. These entities purchase products through
wholesalers at the lower vendor price, and the wholesalers
charge the difference between their acquisition cost and the
lower vendor price back to the Business. Chargebacks are
accounted for by establishing an accrual in an amount equal to
the estimate of chargeback claims. The Business determines
estimates of the chargebacks primarily based on historical
experience regarding chargebacks and current contract prices
under the vendor programs. The Business considers vendor
payments and claim processing time lags and adjusts the accrual
periodically throughout each period to reflect actual experience
and any changes in business circumstances or trends.
Managed
Health Care Rebates and Other Contract Discounts
The Business offers rebates and discounts to managed health care
organizations and to other contract counterparties such as
hospitals and group purchasing organizations in the
U.S. Managed health care rebates and other contract
discounts are accounted for by establishing an accrual in an
amount equal to the estimate of managed health care rebates and
other contract discounts. Estimates of the managed health care
rebates and other contract discounts accruals are determined
primarily based on historical experience regarding these rebates
and discounts and current contract prices. The Business also
considers the current and historical prescription activity
provided by external sources, current contract prices and any
expected contract changes and adjusts the accrual periodically
throughout each period to reflect actual experience and any
changes in business circumstances or trends.
Costs
and Expenses
Cost of products sold includes manufacturing costs, amortization
of acquired technology and product rights, and royalty expenses.
Research and development costs are expensed as incurred. Direct
advertising expenses incurred by the Business are minimal in
nature. Other advertising expenses are incurred by Organon and
recharged to the Business, which are included in selling,
general and administrative expenses in the statement of
operations. The Business does not have visibility with respect
to the exact amounts related to advertising incurred and charged
by Organon.
Income
Taxes
The Business does not file separate tax returns but rather is
included in the income tax returns filed by Ligand in various
domestic and foreign jurisdictions. For purposes of these
unaudited historical carve-out financial statements, the tax
provision of the Business was determined from the AVINZA
financial information carved out of the consolidated financial
statements of Ligand, including allocations deemed necessary by
management as though the Business were filing its own tax return.
The Business recognizes liabilities or assets for the deferred
tax consequences of temporary differences between the tax bases
of assets or liabilities and their reported amounts in the
financial statements in accordance with SFAS No. 109,
Accounting for Income Taxes (SFAS 109).
These temporary differences will result in taxable or deductible
amounts in future years when the reported amounts of the assets
or liabilities are recovered or settled. SFAS 109 requires
that a valuation allowance be established when management
determines that it is more likely than not that all or a portion
of a deferred tax asset will not be realized. The Business
evaluates the realizability of its net deferred tax assets and
valuation allowances are provided, as necessary. During this
evaluation, the Business reviews its forecasts of income in
conjunction with other positive and negative evidence
surrounding the realizability of its deferred tax assets to
determine if a valuation allowance is required. Adjustments to
the valuation allowance will increase or decrease the
Business income tax provision or benefit.
60
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Accounting
for Stock-Based Compensation
The Business employees participate in various Ligand stock
compensation plans. Prior to January 1, 2006, Ligand
accounted for stock-based compensation in accordance with
Accounting Principles Board Opinion No. 25, Accounting
for Stock Issued to Employees (APB No. 25),
and related interpretations and Financial Accounting Standards
Board (FASB) Interpretation No. 44,
Accounting for Certain Transactions Involving Stock
Compensation (FIN No. 44).
Accordingly, the Business also applied APB No. 25 to
account for awards to its employees under Ligand stock
compensation plans. Under the intrinsic-value method prescribed
by APB No. 25, the Business recognized compensation expense
for awards to the Business employees only when it granted
stock-based compensation with an option exercise price that was
lower than the fair value of the underlying stock. Historically,
stock options were granted to employees of the Business with an
exercise price equal to the market value of the underlying
common stock on the date of the grant; therefore, no
compensation expense was recorded prior to January 1, 2006.
Effective January 1, 2006, the Business adopted
SFAS No. 123 (revised 2004), Share-Based Payment
(SFAS No. 123(R)), which requires the
measurement and recognition of compensation expense for all
share-based payment awards made to employees and directors based
on estimated fair values. SFAS No. 123(R)replaced the
existing SFAS No. 123 and supersedes the
Business previous accounting under APB No. 25. In
March 2005, the Securities and Exchange Commission issued
SAB No. 107 (SAB No. 107)
relating to SFAS No. 123(R). The Business has applied
the provisions of SAB No. 107 in its adoption of
SFAS No. 123(R).
The Business adopted SFAS No. 123(R) using the
modified prospective transition method. In accordance with the
modified prospective transition method, the Business
financial statements for prior periods have not been restated to
reflect, and do not include, the impact of
SFAS No. 123(R). Compensation cost recognized in 2006
includes: (a) compensation cost for all share-based
payments granted prior to, but not yet vested as of
January 1, 2006, based on the grant date fair value
estimated in accordance with the original provisions of
SFAS No. 123, and (b) compensation cost for all
share-based payments granted in 2006, based on grant date fair
value estimated in accordance with the provisions of
SFAS 123(R).
In accordance with SFAS No. 148, Accounting for
Stock-Based Compensation-Transition and Disclosure
(SFAS No. 148), the following table
summarizes the Business results on a pro forma basis as if
it had recorded compensation expense for Ligand employees that
provide direct and indirect support to the Business based upon
the fair value at the grant date for awards under these plans
consistent with the methodology prescribed under
SFAS No. 123 for the six months ended June 30,
2005 and for the years ended December 31, 2005, 2004 and
2003 (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Six Months
|
|
|
|
|
|
|
Ended
|
|
|
|
|
|
|
June 30,
|
|
|
Years Ended December 31,
|
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Net income (loss), as reported
|
|
$
|
34
|
|
|
$
|
(819
|
)
|
|
$
|
(29,190
|
)
|
|
$
|
(34,664
|
)
|
Stock-based employee compensation
included in reported net loss
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Less: total stock-based
compensation expense determined under fair value method for all
awards continuing to vest
|
|
|
(161
|
)
|
|
|
(307
|
)
|
|
|
(775
|
)
|
|
|
(616
|
)
|
Less: total stock-based
compensation expense determined under fair value based method
for options accelerated in January 2005(1)
|
|
|
(2,025
|
)
|
|
|
(2,025
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss, pro forma
|
|
$
|
(2,152
|
)
|
|
$
|
(3,151
|
)
|
|
$
|
(29,965
|
)
|
|
$
|
(35,280
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1) |
|
Represents pro forma unrecognized expense for accelerated
options as of the date of acceleration. Total compensation
expense for stock-based compensation for the six months ended
June 30, 2006 was approximately $0.2 million. There
was no deferred tax benefit recognized in connection with this
cost. |
61
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Options were also granted to non-employee consultants that
provided direct support to the Business. Fair value of options
granted to non-employee consultants are accounted for under
Emerging Issues Task Force (EITF)
96-18,
Accounting for Equity Instruments That Are Issued to Other
Than Employees for Acquiring, or in Conjunction With Selling,
Goods or Services. Options granted to non-employee
consultants generally vest between 24 and 36 months. All
option awards generally expire ten years from the date of the
grant. Stock-based compensation cost for awards to employees is
recognized on a straight-line basis over the vesting period
until the last tranche vests. Compensation cost for consultant
awards is recognized over each separate tranches vesting
period.
The Black-Scholes option pricing valuation model was developed
for use in estimating the fair value of stock option grants
awarded to employees and directors that have no vesting
restrictions and are fully transferable with the assumptions
listed in the below table. The expected term of the employee
options is the estimated weighted-average period until exercise
or cancellation of vested options (forfeited unvested options
are not considered). As permitted by SAB No. 107
guidance, the Business used the safe harbor expected
term assumption for grants up to December 31, 2007, based
on the mid-point of the period between vesting date and
contractual term, averaged on a
tranche-by-tranche basis.
The Business used the safe harbor in selecting the expected term
assumption in 2006. The expected term for consultant awards is
the remaining period to contractual expiration. In selecting the
assumption for future volatility, the Business used the
historical volatility of Ligands stock price over a period
equal to the expected term. The assumptions used and fair values
of such awards are indicative of a Ligand stock option and may
not necessarily be representative of the value of a comparable
award granted by the Business.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Six Months Ended June 30,
|
|
|
Years Ended December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Risk-free interest rates
|
|
|
4.70
|
%
|
|
|
3.70
|
%
|
|
|
4.35
|
%
|
|
|
3.61
|
%
|
|
|
3.25
|
%
|
Dividend yields
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Expected volatility
|
|
|
70
|
%
|
|
|
73
|
%
|
|
|
72
|
%
|
|
|
74
|
%
|
|
|
72
|
%
|
Weighted average expected life
|
|
|
6
|
yrs
|
|
|
5
|
yrs
|
|
|
5
|
yrs
|
|
|
5
|
yrs
|
|
|
5
|
yrs
|
On January 31, 2005, Ligand accelerated the vesting of
certain unvested and
out-of-the-money
stock options previously awarded to certain employees of the
Business under Ligands 1992 and 2002 stock option plans
which had an exercise price greater than $10.41, the closing
price of Ligands stock on that date. The vesting for
options to purchase approximately 0.3 million shares of
common stock held by employees of the Business were accelerated.
Holders of incentive stock options (ISOs) within the
meaning of Section 422 of the Internal Revenue Code of
1986, as amended, were given the election to decline the
acceleration of their options if such acceleration would have
the effect of changing the status of such option for federal
income tax purposes from an ISO to a non-qualified stock option.
In addition, executive officers plus other members of Ligand
senior management agreed that they will not sell any shares
acquired through the exercise of an accelerated option prior to
the date on which the exercise would have been permitted under
the options original vesting terms. This agreement does
not apply to a) shares sold in order to pay applicable
taxes resulting from the exercise of an accelerated option or
b) upon the officers retirement or other termination
of employment.
The purpose of the acceleration was to eliminate any future
compensation expense that Ligand would have otherwise recognized
in its statement of operations with respect to these options
upon the implementation of SFAS 123(R).
Employees
Stock Purchase Plan
Ligand also has an employee stock purchase plan (the 2002
ESPP). The 2002 ESPP was originally adopted July 1,
2001 and amended through June 30, 2003 to allow employees
to purchase a limited amount of common stock at the end of each
three month period at a price equal to the lesser of 85% of fair
market value on a) the first trading
62
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
day of the period, or b) the last trading day of the period
(the Lookback Provision). The 15% discount and the
Lookback Provision make the plan compensatory under
SFAS 123(R). Since the adoption in 2002, a total of
510,248 shares of common stock have been reserved for
issuance by Ligand under the 2002 ESPP (includes shares
transferred from the predecessor plan). As of June 30,
2006, 60,028 shares of common stock had been issued under
the 2002 ESPP to Ligand employees that provided direct support
to the Business and 147,510 shares are available for future
issuance to all Ligand employees. For the six months ended
June 30, 2006, there were no issuances of common shares
under the ESPP to the Ligand employees that provided direct
support to the Business.
Segment
Reporting
The Business represents a single operating segment.
|
|
Note 3:
|
Balance
Sheet Details
|
Balance sheet details as of June 30, 2006 and
December 31, 2005 and 2004 are as follows:
Accounts receivable consist of the following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Trade accounts receivable
|
|
$
|
3,406
|
|
|
$
|
1,588
|
|
|
$
|
19,730
|
|
Due from finance company
|
|
|
9,209
|
|
|
|
13,788
|
|
|
|
3,415
|
|
Less discounts and allowances
|
|
|
(542
|
)
|
|
|
(534
|
)
|
|
|
(637
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
12,073
|
|
|
$
|
14,842
|
|
|
$
|
22,508
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other current assets consist of the following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Deferred royalty cost
|
|
$
|
3,604
|
|
|
$
|
3,890
|
|
|
$
|
4,444
|
|
Deferred cost of products sold
|
|
|
4,860
|
|
|
|
4,432
|
|
|
|
3,552
|
|
Prepaid insurance
|
|
|
207
|
|
|
|
466
|
|
|
|
393
|
|
Prepaid other
|
|
|
464
|
|
|
|
1,205
|
|
|
|
342
|
|
Other
|
|
|
40
|
|
|
|
24
|
|
|
|
55
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
9,175
|
|
|
$
|
10,017
|
|
|
$
|
8,786
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Accrued liabilities consist of the following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2004
|
|
|
Allowances for loss on returns,
rebates, chargebacks and other discounts
|
|
$
|
10,737
|
|
|
$
|
11,485
|
|
|
$
|
10,159
|
|
Co-promotion
|
|
|
14,406
|
|
|
|
24,778
|
|
|
|
7,845
|
|
Distribution services
|
|
|
2,166
|
|
|
|
2,435
|
|
|
|
1,939
|
|
Compensation
|
|
|
1,531
|
|
|
|
1,631
|
|
|
|
938
|
|
Royalties
|
|
|
1,124
|
|
|
|
1,398
|
|
|
|
2,394
|
|
Other
|
|
|
6
|
|
|
|
204
|
|
|
|
1,352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
29,970
|
|
|
$
|
41,931
|
|
|
$
|
24,627
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
63
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
The following summarizes the activity in the accrued liability
accounts related to allowances for loss on returns, rebates,
chargebacks and other discounts (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Losses on
|
|
|
|
|
|
Managed
|
|
|
|
|
|
|
|
|
|
|
|
|
Returns
|
|
|
|
|
|
Care
|
|
|
|
|
|
|
|
|
|
|
|
|
Due to
|
|
|
|
|
|
Rebates
|
|
|
|
|
|
|
|
|
|
|
|
|
Changes
|
|
|
Medicaid
|
|
|
and Other
|
|
|
Charge-
|
|
|
Other
|
|
|
|
|
|
|
In Price
|
|
|
Rebates
|
|
|
Rebates
|
|
|
Backs
|
|
|
Discounts
|
|
|
Total
|
|
|
Balance at January 1, 2003
|
|
$
|
190
|
|
|
$
|
16
|
|
|
$
|
31
|
|
|
$
|
|
|
|
$
|
46
|
|
|
$
|
283
|
|
Provision
|
|
|
2,389
|
|
|
|
1,732
|
|
|
|
852
|
|
|
|
70
|
|
|
|
4,335
|
|
|
|
9,378
|
|
Payments
|
|
|
|
|
|
|
(368
|
)
|
|
|
(457
|
)
|
|
|
(61
|
)
|
|
|
(4,293
|
)
|
|
|
(5,179
|
)
|
Charges
|
|
|
(213
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(213
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2003
|
|
|
2,366
|
|
|
|
1,380
|
|
|
|
426
|
|
|
|
9
|
|
|
|
88
|
|
|
|
4,269
|
|
Provision
|
|
|
2,830
|
|
|
|
12,988
|
|
|
|
5,721
|
|
|
|
372
|
|
|
|
2,628
|
|
|
|
24,539
|
|
Payments
|
|
|
|
|
|
|
(9,766
|
)
|
|
|
(4,454
|
)
|
|
|
(381
|
)
|
|
|
(2,716
|
)
|
|
|
(17,317
|
)
|
Charges
|
|
|
(1,332
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1,332
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2004
|
|
|
3,864
|
|
|
|
4,602
|
|
|
|
1,693
|
|
|
|
|
|
|
|
|
|
|
|
10,159
|
|
Provision
|
|
|
911
|
|
|
|
17,412
|
|
|
|
10,331
|
|
|
|
345
|
|
|
|
|
|
|
|
28,999
|
|
Payments
|
|
|
|
|
|
|
(17,128
|
)
|
|
|
(8,691
|
)
|
|
|
(145
|
)
|
|
|
|
|
|
|
(25,964
|
)
|
Charges
|
|
|
(1,709
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1,709
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2005
|
|
|
3,066
|
|
|
|
4,886
|
|
|
|
3,333
|
|
|
|
200
|
|
|
|
|
|
|
|
11,485
|
|
Provision
|
|
|
1,552
|
|
|
|
2,586
|
|
|
|
6,277
|
|
|
|
237
|
|
|
|
|
|
|
|
10,652
|
|
Payments
|
|
|
|
|
|
|
(5,896
|
)
|
|
|
(3,054
|
)
|
|
|
(429
|
)
|
|
|
|
|
|
|
(9,379
|
)
|
Charges
|
|
|
(2,021
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(2,021
|
)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at June 30, 2006
|
|
$
|
2,597
|
|
|
$
|
1,576
|
|
|
$
|
6,556
|
|
|
$
|
8
|
|
|
$
|
|
|
|
$
|
10,737
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Note 4:
|
Corporate
Expense Allocations
|
The Business receives services and support functions from
Ligand. The Business operations are dependant upon
Ligands ability to perform these services and support
functions. The costs associated with these services and support
functions have been allocated to the Business using
methodologies established by the Companys management and
considered to be a reasonable reflection of the utilization of
services provided to the Business. Allocations for research and
development expenses are based primarily on headcount.
Allocations for selling expenses are based primarily on
headcount. Allocations for general and administration expenses
are based primarily on proportionate operating expenses adjusted
for non-cash expenses. The financial information included herein
may not reflect the financial position, the results of
operations and cash flows of the Business in the future or had
the Business been a separate, stand-alone entity during the
periods presented.
Expense allocations for the following periods were (in
thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Corporate functions, finance,
legal and treasury
|
|
$
|
6,393
|
|
|
$
|
3,162
|
|
|
$
|
7,733
|
|
|
$
|
3,450
|
|
|
$
|
2,544
|
|
Govt affairs, health and
environmental services
|
|
|
111
|
|
|
|
108
|
|
|
|
227
|
|
|
|
158
|
|
|
|
67
|
|
Information technology
|
|
|
369
|
|
|
|
339
|
|
|
|
712
|
|
|
|
502
|
|
|
|
248
|
|
Other operational and
infrastructure charges
|
|
|
664
|
|
|
|
616
|
|
|
|
1,356
|
|
|
|
959
|
|
|
|
588
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
7,537
|
|
|
$
|
4,225
|
|
|
$
|
10,028
|
|
|
$
|
5,069
|
|
|
$
|
3,447
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
64
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Corporate expense allocations as presented in the statements of
operations, for the following periods were (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30,
|
|
|
December 31,
|
|
|
|
2006
|
|
|
2005
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Research and development
|
|
$
|
133
|
|
|
$
|
182
|
|
|
$
|
586
|
|
|
$
|
589
|
|
|
$
|
70
|
|
Selling, general and administration
|
|
|
7,404
|
|
|
|
4,043
|
|
|
|
9,442
|
|
|
|
4,480
|
|
|
|
3,377
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
7,537
|
|
|
$
|
4,225
|
|
|
$
|
10,028
|
|
|
$
|
5,069
|
|
|
$
|
3,447
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Note 5:
|
Accounts
Receivable Factoring Arrangement
|
During 2003, Ligand entered into a one-year accounts receivable
factoring arrangement under which eligible accounts receivable
of the Business are sold without recourse to a finance company.
The agreement was renewed for a one-year period in the second
quarter of 2004 and again in the second quarter of 2005 through
December 2007. Commissions on factored receivables are paid
based on the gross receivables sold, subject to a minimum annual
commission. Additionally, the Business pays interest on the net
outstanding balance of the uncollected factored accounts
receivable at an interest rate equal to the JPMorgan Chase Bank
prime rate. The Business continues to service the factored
receivables. The servicing expenses for the six months ended
June 30, 2006 and 2005 and for the years ended
December 31, 2005, 2004 and 2003 and the servicing
liability at June 30, 2006 and December 31, 2005 and
2004 were not material. There were no material gains or losses
on the sale of such receivables. The Business accounts for the
sale of receivables under this arrangement in accordance with
SFAS No. 140, Accounting for Transfers and
Servicing of Financial Assets and Extinguishment of Liabilities
(SFAS No. 140).
|
|
Note 6:
|
Elan
License and Supply Agreement
|
In 1998, Elan agreed to exclusively license and supply to the
Business in the United States and Canada its proprietary product
AVINZA, a form of morphine for chronic,
moderate-to-severe
pain. In November 2002, the Business and Elan agreed to amend
the terms of the AVINZA license and supply agreement. Under the
terms of the amendment, Ligand paid Elan $100.0 million in
return for a reduction in Elans product supply price on
sales of AVINZA by Ligand, rights to sublicense and obtain a
co-promotion partner in its territories, and rights to qualify
and purchase AVINZA from a second manufacturing source.
Elans adjusted royalty and supply price of AVINZA is
approximately 10% of the products net sales, compared to
approximately 30-35% in the prior agreement. Ligand committed to
place firm purchase orders for a minimum of 40 batches of AVINZA
from Elan annually through 2005, estimated at approximately
$9.2 million per year. In addition, Elan agreed to forego
its option to co-promote AVINZA in the United States and
Canada. The amount paid to Elan and related transaction costs
were capitalized as acquired technology and product rights.
In 2005, 2004, and 2003, purchases and royalties under the
agreement totaled $12.4 million, $15.4 million, and
$6.3 million, respectively. The purchases in 2003 represent
20 batches of product. Elan was unable to obtain a sufficient
quota of morphine from the Drug Enforcement Agency and was
therefore only able to supply Ligand with 20 batches prior to
December 31, 2003. The remaining batches were subsequently
shipped to Ligand in 2004. Ligand met its commitment for placing
firm purchase orders for 2005 and 2004.
65
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
|
|
Note 7:
|
AVINZA
Co-promotion
|
In February 2003, Ligand and Organon announced that they had
entered into an agreement for the co-promotion of AVINZA. Under
the terms of the agreement, Organon committed to a specified
minimum number of primary and secondary product calls delivered
to certain high prescribing physicians and hospitals beginning
in March 2003. Organons compensation was structured as a
percentage of net sales based on generally accepted accounting
principles (GAAP), which paid Organon for their
efforts and also provided Organon an economic incentive for
performance and results. In exchange, Ligand paid Organon a
percentage of AVINZA net sales based on the following schedule:
|
|
|
|
|
% of Incremental Net Sales
|
Annual Net Sales of AVINZA
|
|
Paid to Organon by Ligand
|
|
$0-150 million
|
|
30% (0% for 2003)
|
$150-300 million
|
|
40%
|
$300-425 million
|
|
50%
|
> $425 million
|
|
45%
|
In January 2006, Ligand signed an agreement with Organon that
terminated the AVINZA co-promotion agreement between the two
companies and returned AVINZA co-promotion rights to Ligand. The
effective date of the termination agreement was January 1,
2006; however, the parties agreed to continue to cooperate
during a transition period ending September 30, 2006 (the
Transition Period) to promote the product. The
Transition Period co-operation includes a minimum number of
product sales calls per quarter (100,000 for Organon and 30,000
for Ligand with an aggregate of 375,000 and 90,000,
respectively, for the Transition Period) as well as the
transition of ongoing promotions, managed care contracts,
clinical trials and key opinion leader relationships to Ligand.
During the Transition Period, Ligand agreed to pay Organon an
amount equal to 23% of AVINZA net sales as reported by Ligand.
Ligand also paid and was responsible for the design and
execution of all clinical, advertising and promotion expenses
and activities.
Additionally, in consideration of the early termination and
return of rights under the terms of the agreement, Ligand agreed
to unconditionally pay Organon $37.8 million on or before
October 15, 2006. Ligand will further pay Organon
$10.0 million on or before January 15, 2007, provided
that Organon has made its minimum required level of sales calls.
Under certain conditions, including change of control, the cash
payments will accelerate. In addition, after the termination,
Ligand will make quarterly payments to Organon equal to 6.5% of
AVINZA net sales through December 31, 2012 and thereafter
6.0% through patent expiration, currently anticipated to be
November of 2017 (see Note 12).
The unconditional payment of $37.8 million to Organon and
the estimated fair value of the amounts to be paid to Organon
after the termination ($95.2 million as of January 1,
2006), based on the net sales of the product (currently
anticipated to be paid quarterly through November
2017) were recognized as liabilities and expensed as costs
of the termination as of the effective date of the agreement,
January 2006. Additionally, the conditional payment of
$10.0 million, which represents an approximation of the
fair value of the service element of the agreement during the
Transition Period (when the provision to pay 23% of AVINZA net
sales is also considered), is being recognized ratably as
additional co-promotion expense over the Transition Period. For
the six months ended June 30, 2006, the pro-rata
recognition of this element of co-promotion expense amounted to
$6.6 million, respectively.
Although the quarterly payments to Organon will be based on net
reported AVINZA product sales, such payments will not result in
current period expense in the period upon which the payment is
based, but instead will be charged against the co-promote
termination liability. The liability will be adjusted at each
reporting period to fair value and will be recognized, utilizing
the interest method, as other non-operating expense (interest
expense) for that period at a rate of 15%, the discount rate
used to initially value this component of the termination
liability. Additionally, any changes to the Business
estimates of future net AVINZA product sales will result in a
change to
66
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
the liability which will be recognized as an increase or
decrease to earnings in the period such changes are identified.
Accreted interest expense for the six months ended June 30,
2006 was $6.8 million.
On a quarterly basis, management reviews the carrying value of
the co-promote termination liability. Due to assumptions and
judgments inherent in determining the estimates of future net
AVINZA sales through November 2017, the actual amount of net
AVINZA sales used to determine the current fair value of the
Business co-promote termination liability may be
materially different from its current estimates. In addition,
because of the inherent difficulties of predicting possible
changes to the estimates and assumptions used to determine the
estimate of future AVINZA product sales, the Business is unable
to quantify an estimate of the reasonably likely effect of any
such changes on its results of operations or financial position.
For the six-month period ended June 30, 2006, the Business
recorded a reduction in the co-promote termination liability and
a corresponding increase to earnings of $0.4 million based
on the Business updated estimate of future AVINZA net
sales.
The components of the co-promote termination liability as of
June 30, 2006 are as follows (in thousands):
|
|
|
|
|
Payment due October 15, 2006
|
|
$
|
37,750
|
|
Net present value of payments
based on estimated future net AVINZA product sales as of
January 1, 2006
|
|
|
95,191
|
|
Reduction in net present value of
liability resulting from updated estimate of net AVINZA product
sales as of June 30, 2006
|
|
|
(434
|
)
|
Accretion of interest expense to
net present value of payments based on net AVINZA product sales
as of June 30, 2006
|
|
|
6,800
|
|
|
|
|
|
|
|
|
|
139,307
|
|
Less: current portion of
co-promote termination liability
|
|
|
(45,046
|
)
|
|
|
|
|
|
Long-term portion of co-promote
termination liability
|
|
|
94,261
|
|
|
|
|
|
|
|
|
Note 8:
|
Commitments
and Contingencies
|
Equipment
Financing
The Company has entered into capital lease and equipment note
payable agreements. Such agreements have been allocated to the
Business based on the specific equipment utilized by the
Business. Such agreements require monthly payments through
December 2009 including interest ranging from 7.35% to 10.11%.
The carrying value of equipment under these agreements allocated
to the Business at December 31, 2005 and 2004 was
$0.8 million and $0.8 million, respectively. At
December 31, 2005 and 2004, related accumulated
amortization was $0.4 million and $0.3 million,
respectively. The underlying equipment is used as collateral
under the equipment notes payable.
67
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
At December 31, 2005 annual minimum payments due under the
Business portion of the Companys equipment lease
obligations are as follows (in thousands):
|
|
|
|
|
|
|
Obligations Under
|
|
|
|
Capital Leases and
|
|
|
|
Equipment Notes Payable
|
|
|
2006
|
|
$
|
303
|
|
2007
|
|
|
302
|
|
2008
|
|
|
118
|
|
2009
|
|
|
11
|
|
2010 and thereafter
|
|
|
|
|
|
|
|
|
|
Total minimum lease payments
|
|
|
734
|
|
Less: amounts representing interest
|
|
|
(58
|
)
|
|
|
|
|
|
Present value of minimum lease
payments
|
|
|
676
|
|
Less: current portion
|
|
|
(270
|
)
|
|
|
|
|
|
|
|
$
|
406
|
|
|
|
|
|
|
Product
Liability
AVINZA is subject to potential product liability risks. AVINZA
also may need to be recalled to address regulatory issues. A
successful product liability claim or series of claims brought
against the Business could result in payment of significant
amounts of money and divert managements attention from
running the business. The Business may not be able to maintain
insurance on acceptable terms, or the insurance may not provide
adequate protection in the case of a product liability claim. To
the extent that product liability insurance, if available, does
not cover potential claims, the Business would be required to
self-insure the risks associated with such claims. The Business
believes that it carries reasonably adequate insurance for
product liability claims. Costs associated with product
liability insurance are included in the statement of operations.
Distribution
Service and Product Manufacturing Agreements
In 2004, the Business entered into one-year
fee-for-service
agreements (or distribution service agreements) for its product
with the majority of its wholesaler customers. These agreements
were subsequently renewed in 2005 for an additional one-year
period. In exchange for a set fee, the wholesalers agreed to
provide the Business with certain information regarding product
stocking and out-movement; agreed to maintain inventory
quantities within specified minimum and maximum levels;
inventory handling, stocking and management services; and
certain other services surrounding the administration of returns
and chargebacks. The amount of minimum payments due under the
distribution service agreements for 2006 is approximately
$3.2 million.
For the six months ended June 30, 2006, shipments to three
wholesale distributors accounted for 31%, 29% and 28%,
respectively, of total shipments. For the year ended
December 31, 2005, shipments to four wholesale distributors
accounted for 27%, 27%, 17% and 16%, respectively, of total
shipments. For the year ended December 31, 2004, shipments
to four wholesale distributors accounted for 29%, 24%, 18% and
17%, respectively, of total shipments
As of December 31, 2004, Elan was the Business only
approved supplier of AVINZA. In March 2004, Ligand entered into
a five-year manufacturing and packaging agreement with Cardinal
Health PTS, LLC (Cardinal) under which Cardinal will
manufacture AVINZA at its Winchester, Kentucky facility. In
August 2005, the FDA approved the production of AVINZA at the
Cardinal facility. Under the terms of the agreement, Ligand
committed to certain minimum annual purchases ranging from
approximately $1.6 million to $2.3 million.
68
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
|
|
Note 9:
|
Stock
Compensation
|
Stock
Plans
Certain Ligand employees that provided direct support to the
Business participate in Ligands various incentive award
plans. The following is a description of the terms of such plans:
Incentive
Plans
Stock incentive awards are provided to certain Ligand employees
under terms of Ligands 2002 Stock Incentive Plan which
contains four separate equity programs Discretionary
Option Grant Program, Automatic Option Grant Program, Stock
Issuance Program and Director Fee Option Grant Program
(the 2002 Plan). As of June 30, 2006, options
for 621,109 shares of common stock were outstanding under
the 2002 plan related to Ligand employees that provide direct
support to the Business and 545,101 shares remained
available for future option grant or direct issuance for all
Ligand employees.
69
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Stock
Option Activity
The following table summarizes option activity under the Plans
for certain Ligand employees that provided direct support to the
Business:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted
|
|
|
|
|
|
|
|
|
|
|
|
|
Average
|
|
|
|
|
|
|
|
|
|
Weighted
|
|
|
Remaining
|
|
|
Aggregate
|
|
|
|
|
|
|
Average
|
|
|
Contractual
|
|
|
Intrinsic
|
|
|
|
|
|
|
Exercise
|
|
|
Term in
|
|
|
Value
|
|
|
|
Shares
|
|
|
Price
|
|
|
Years
|
|
|
(In thousands)
|
|
|
Balance at January 1, 2003
|
|
|
375,686
|
|
|
$
|
12.812
|
|
|
|
|
|
|
|
|
|
Granted
|
|
|
200,432
|
|
|
|
9.935
|
|
|
|
|
|
|
|
|
|
Exercised
|
|
|
(19,606
|
)
|
|
|
10.880
|
|
|
|
|
|
|
|
|
|
Forfeited
|
|
|
(97,802
|
)
|
|
|
11.784
|
|
|
|
|
|
|
|
|
|
Cancelled
|
|
|
(54,979
|
)
|
|
|
15.663
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2003
|
|
|
403,731
|
|
|
$
|
11.338
|
|
|
|
8.186
|
|
|
$
|
1,476
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercisable at December 31,
2003
|
|
|
158,496
|
|
|
$
|
11.889
|
|
|
|
6.841
|
|
|
$
|
508
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at January 1, 2004
|
|
|
403,731
|
|
|
$
|
11.338
|
|
|
|
|
|
|
|
|
|
Granted
|
|
|
242,464
|
|
|
|
14.122
|
|
|
|
|
|
|
|
|
|
Exercised
|
|
|
(20,333
|
)
|
|
|
8.965
|
|
|
|
|
|
|
|
|
|
Forfeited
|
|
|
(49,689
|
)
|
|
|
12.627
|
|
|
|
|
|
|
|
|
|
Cancelled
|
|
|
(10,686
|
)
|
|
|
15.429
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2004
|
|
|
565,487
|
|
|
$
|
12.373
|
|
|
|
8.076
|
|
|
$
|
678
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercisable at December 31,
2004
|
|
|
227,306
|
|
|
$
|
11.840
|
|
|
|
6.402
|
|
|
$
|
333
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at January 1, 2005
|
|
|
565,487
|
|
|
$
|
12.373
|
|
|
|
|
|
|
|
|
|
Granted
|
|
|
114,410
|
|
|
|
8.904
|
|
|
|
|
|
|
|
|
|
Exercised
|
|
|
(2,052
|
)
|
|
|
5.182
|
|
|
|
|
|
|
|
|
|
Forfeited
|
|
|
(31,461
|
)
|
|
|
9.563
|
|
|
|
|
|
|
|
|
|
Cancelled
|
|
|
(57,304
|
)
|
|
|
12.815
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at December 31, 2005
|
|
|
589,080
|
|
|
$
|
11.843
|
|
|
|
7.444
|
|
|
$
|
743
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercisable at December 31,
2005
|
|
|
481,740
|
|
|
$
|
12.810
|
|
|
|
6.889
|
|
|
$
|
405
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at January 1, 2006
|
|
|
589,080
|
|
|
$
|
11.843
|
|
|
|
|
|
|
|
|
|
Granted
|
|
|
120,938
|
|
|
|
11.296
|
|
|
|
|
|
|
|
|
|
Exercised
|
|
|
(13,729
|
)
|
|
|
8.335
|
|
|
|
|
|
|
|
|
|
Forfeited
|
|
|
(18,345
|
)
|
|
|
9.082
|
|
|
|
|
|
|
|
|
|
Cancelled
|
|
|
(56,835
|
)
|
|
|
13.778
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance at June 30, 2006
|
|
|
621,109
|
|
|
$
|
11.724
|
|
|
|
7.352
|
|
|
$
|
197
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Exercisable at June 30, 2006
|
|
|
412,778
|
|
|
$
|
12.536
|
|
|
|
6.423
|
|
|
$
|
141
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Options expected to vest as of
June 30, 2006
|
|
|
604,007
|
|
|
$
|
11.793
|
|
|
|
7.296
|
|
|
$
|
191
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
70
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
The following table summarizes significant ranges of outstanding
and exercisable options as of June 30, 2006 for Ligand
employees that provided direct support to the Business:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Options Outstanding
|
|
|
Options Exercisable
|
|
|
|
|
|
|
|
Weighted-
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Average
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Remaining
|
|
|
Weighted Average
|
|
|
|
|
|
Weighted Average
|
|
|
|
|
Number
|
|
|
Contractual Term in
|
|
|
Exercise Price
|
|
|
|
|
|
Exercise Price
|
|
Range of Exercise Prices
|
|
|
Outstanding
|
|
|
Years
|
|
|
Per Share
|
|
|
Number Exercisable
|
|
|
Per Share
|
|
|
$
|
1.8232 - $ 9.2500
|
|
|
|
143,273
|
|
|
|
7.152
|
|
|
$
|
7.3290
|
|
|
|
94,047
|
|
|
$
|
7.1919
|
|
$
|
9.3125 - $11.3500
|
|
|
|
132,066
|
|
|
|
8.412
|
|
|
|
10.437
|
|
|
|
45,107
|
|
|
|
10.275
|
|
$
|
11.3750 - $12.5000
|
|
|
|
114,754
|
|
|
|
8.167
|
|
|
|
11.943
|
|
|
|
43,573
|
|
|
|
11.989
|
|
$
|
12.5400 - $15.6300
|
|
|
|
159,534
|
|
|
|
6.231
|
|
|
|
14.080
|
|
|
|
158,867
|
|
|
|
14.080
|
|
$
|
16.0625 - $20.7000
|
|
|
|
71,482
|
|
|
|
6.500
|
|
|
|
17.917
|
|
|
|
71,184
|
|
|
|
17.917
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
1.8232 - $20.7000
|
|
|
|
621,109
|
|
|
|
7.352
|
|
|
$
|
11.724
|
|
|
|
412,778
|
|
|
$
|
12.536
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The estimated weighted average fair value at grant date for the
options granted for the six months ended June 30, 2006 and
2005 and for the year ended December 31, 2005, 2004, 2003
was $11.30, $7.84, $8.90, $14.12, and $9.94 per option,
respectively. The total intrinsic value of all options exercised
during the six months ended June 30, 2006 was
$0.02 million. As of June 30, 2006, there was
approximately $0.74 million of total unrecognized
compensation cost related to nonvested stock options. That cost
is expected to be recognized over a weighted average period of
2.95 years.
Cash received from options exercised for the six months ended
June 30, 2006 and 2005 was approximately $13,000 and
$11,000, respectively. There is no current tax benefit related
to options exercised because of net operating losses
(NOLs) for which a full valuation allowance has been
established.
The Business operating results have historically been
included in Ligands consolidated U.S. federal and
state income tax returns and
non-U.S. jurisdictions
tax returns. The provisions for income taxes in the combined
financial statements have been determined on a separate return
basis. The Business assesses the realization of its net deferred
tax assets and the need for a valuation allowance on a separate
return basis, and excludes from that assessment any utilization
of those losses by Ligand. This assessment requires that the
Business management make judgments about benefits that
could be realized from the future taxable income, as well as
other positive and negative factors influencing the realization
of deferred tax assets. Due to the cumulative losses by the
Business, a valuation against any net deferred assets was
recorded. The Business intends to maintain a full valuation
allowance until sufficient positive evidence exists to support
reversal of the valuation allowance. All tax return attributes
generated, as calculated on a separate return methodology not
used by Ligand historically, will be retained by Ligand.
71
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Thee components of the income tax provision are as follows (in
thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
December 31,
|
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Current provision:
|
|
|
|
|
|
|
|
|
|
|
|
|
Federal
|
|
$
|
9,677
|
|
|
$
|
7,155
|
|
|
$
|
1,105
|
|
State
|
|
|
2,338
|
|
|
|
1,797
|
|
|
|
417
|
|
Foreign
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
12,015
|
|
|
|
8,952
|
|
|
|
1,522
|
|
Deferred provision:
|
|
|
|
|
|
|
|
|
|
|
|
|
Federal
|
|
|
|
|
|
|
|
|
|
|
|
|
State
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
12,015
|
|
|
$
|
8,952
|
|
|
$
|
1,522
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
On a stand-alone basis, the Business does not have net operating
loss carry forwards or research and development credits.
Accordingly, the Business recorded a current tax provision for
the estimated tax liability it would have on a stand-alone basis
for the periods presented.
Significant components of the Business deferred tax assets
and liabilities for the year ended December 31, 2005 and
2004 are shown below. A valuation allowance has been recognized
to fully offset the net deferred tax assets as of the years
ended December 31, 2005 and 2004 as realization of such
assets is uncertain.
|
|
|
|
|
|
|
|
|
|
|
December 31,
|
|
|
|
2005
|
|
|
2004
|
|
|
Deferred assets (liabilities):
|
|
|
|
|
|
|
|
|
Capitalized research and
development
|
|
$
|
169
|
|
|
$
|
133
|
|
Fixed assets and intangibles
|
|
|
(232
|
)
|
|
|
(214
|
)
|
Accrued expenses
|
|
|
25,990
|
|
|
|
22,424
|
|
Deferred revenue
|
|
|
17,530
|
|
|
|
13,730
|
|
Other
|
|
|
819
|
|
|
|
629
|
|
|
|
|
|
|
|
|
|
|
|
|
|
44,276
|
|
|
|
36,702
|
|
Valuation allowance for deferred
tax assets net of deferred liabilities
|
|
|
(44,276
|
)
|
|
|
(36,702
|
)
|
|
|
|
|
|
|
|
|
|
Net deferred tax asset
|
|
$
|
|
|
|
$
|
|
|
|
|
|
|
|
|
|
|
|
A reconciliation of income tax expense to the amount computed by
applying the statutory federal income tax rate to the
Business income (loss) before taxes is summarized as
follows (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
December 31,
|
|
|
|
2005
|
|
|
2004
|
|
|
2003
|
|
|
Amounts computed at statutory
federal rate
|
|
$
|
3,919
|
|
|
$
|
(7,083
|
)
|
|
$
|
(11,600
|
)
|
State taxes net of federal benefit
|
|
|
443
|
|
|
|
(406
|
)
|
|
|
(1,900
|
)
|
Meals and entertainment
|
|
|
79
|
|
|
|
103
|
|
|
|
165
|
|
Change in valuation allowance
|
|
|
7,574
|
|
|
|
16,338
|
|
|
|
14,857
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$
|
12,015
|
|
|
$
|
8,952
|
|
|
$
|
1,522
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
72
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
|
|
Note 11:
|
New
Accounting Pronouncements
|
In November 2004, the FASB issued SFAS No. 151,
Inventory Pricing (SFAS 151).
SFAS 151 amends the guidance in Accounting Research
Bulletin (ARB No. 43, Chapter 4,
Inventory Pricing, to clarify the accounting for
abnormal amounts of idle facility expense, freight, handling
costs, and wasted material (spoilage). This statement requires
that those items be recognized as current-period charges. In
addition, SFAS 151 requires that allocation of fixed
production overheads to the costs of conversion be based on the
normal capacity of the production facilities. This statement is
effective for inventory costs incurred during fiscal years
beginning after June 15, 2005. The adoption of
SFAS No. 151 on January 1, 2006 did not have a
material impact on the Business results of operations or
financial position.
In February 2006, the FASB issued SFAS No. 155,
Accounting for Certain Hybrid Financial Instruments
(SFAS 155) which amends
SFAS No. 133, Accounting for Derivative Instruments
and Hedging Activities (SFAS 133) and
SFAS 140, Accounting or the Impairment or Disposal of
Long-Lived Assets (SFAS 140). Specifically,
SFAS 155 amends SFAS 133 to permit fair value
remeasurement for any hybrid financial instrument with an
embedded derivative that otherwise would require bifurcation,
provided the whole instrument is accounted for on a fair value
basis. Additionally, SFAS 155 amends SFAS 140 to allow
a qualifying special purpose entity to hold a derivative
financial instrument that pertains to a beneficial interest
other than another derivative financial instrument.
SFAS 155 applies to all financial instruments acquired or
issued after the beginning of an entitys first fiscal year
that begins after September 15, 2006, with early
application allowed. The adoption of SFAS 155 is not
expected to have a material impact on the Business results
of operations or financial position.
In March 2006, the FASB issued SFAS No. 156,
Accounting for Servicing of Financial Assets
(SFAS 156) to simplify accounting for
separately recognized servicing assets and servicing
liabilities. SFAS 156 amends SFAS No. 140,
Accounting for Transfers and Servicing of Financial Assets
and Extinguishments of Liabilities. Additionally,
SFAS 156 applies to all separately recognized servicing
assets and liabilities acquired or issued after the beginning of
an entitys fiscal year that begins after
September 15, 2006, although early adoption is permitted.
The adoption of SFAS 156 is not expected to have a material
impact on the Business results of operations or financial
position.
In July 2006, the FASB issued FASB Interpretation No. 48
Accounting for Uncertainty in Income Taxes an
interpretation of FASB Statement No. 109
(FIN 48). FIN 48 clarifies the accounting
for uncertainty in income taxes recognized in a companys
financial statements in accordance with SFAS No. 109.
It prescribes a recognition threshold and measurement attribute
for the financial statement recognition and measurement of a tax
position taken or expected to be taken in a tax return.
Additionally, FIN 48 provides guidance on derecognition,
classification, interest and penalties, accounting in interim
periods, disclosure, and transition. FIN 48 is effective
for fiscal years beginning after December 15, 2006. The
adoption of FIN 48 is not expected to have a material
impact on the Business results of operations or financial
position.
On September 15, 2006, the FASB issued Statement
No. 157, Fair Value Measurements
(FAS 157), which addresses how companies
should measure fair value when they are required to use a fair
value measure for recognition or disclosure purposes under
generally accepted accounting principles (GAAP). As
a result of FAS 157 there is a common definition of fair
value to be used throughout GAAP. Companies will need to adopt
FAS 157 for financial statements issued for fiscal years
beginning after November 15, 2007. The Business is
currently evaluating the impact of adopting FAS 157 on the
Business results of operations and financial position.
On September 29, 2006, the FASB issued Statement
No. 158, Employers Accounting for Defined Benefit
Pension and Other Postretirement Plans, an amendment of FASB
Statement No. 87, 88, 106 and 132(R)
(FAS 158). Under FAS 158, companies
must recognize a net liability or asset to report the funded
status of their defined benefit pension and other postretirement
benefit plans (collectively referred to herein as benefit
plans) on their balance sheets, starting with balance
sheets as of December 31, 2006 if they are calendar
year-end public company. FAS 158
73
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
also changed certain disclosures related to benefit plans. The
adoption of FAS 158 is not expected to have a material
impact on the Business results of operations or financial
position.
On September 13, 2006, the SEC staff issued Staff
Accounting Bulletin No. 108 Considering the Effects
of Prior Year Misstatements when Quantifying Misstatements in
Current Year Financial Statements
(SAB 108), which is aimed at
eliminating that diversity in quantification practices with
respect to annual financial statements, and established an
approach that requires quantification of financial statement
errors based on the effects of the error on each of the
companys financial statements and the related disclosures.
This model is commonly referred to as the dual
approach because it essentially requires that errors be
quantified under both the iron-curtain method and the roll-over
method. The Business is currently evaluating the impact of
adopting SAB 108 on its results of operations and financial
position.
|
|
Note 12:
|
Subsequent
Event
|
On September 6, 2006, Ligand and King Pharmaceuticals, Inc.
(King), entered into a Purchase Agreement (the
Purchase Agreement), pursuant to which King agreed
to acquire all of the Companys rights in and to AVINZA in
the United States, its territories and Canada, including,
among other things, all AVINZA inventory, equipment, records and
related intellectual property, and assume certain liabilities as
set forth in the Purchase Agreement (collectively, the
Transaction). In addition, King has, subject to the
terms and conditions of the Purchase Agreement, agreed to offer
employment following the closing of the Transaction (the
Closing) to certain of the Business existing
sales representatives that support the sale of AVINZA or
otherwise reimburse the Company for certain agreed upon
severance arrangements offered to any such non-hired
representatives.
Pursuant to the Purchase Agreement, at Closing, the Company
expects to receive consideration of $312.8 million,
comprised of cash consideration of $265.0 million and the
assumption of payment obligations to Organon Pharmaceuticals USA
Inc. (Organon) of approximately $47.8 million
(or reimbursement to Ligand at closing of the asset sale to the
extent any such amounts have been paid). King will also assume
the Companys existing co-promote termination obligation to
make payments to Organon based on net sales of AVINZA. Of the
$265.0 million cash payment, $15.0 million will be
funded into an escrow account to support any indemnification
claims made by King following the Closing. The Closing Payment
is subject to adjustment based on the Companys ability to
reduce wholesale and retail inventory levels of AVINZA to
certain targeted levels by Closing in accordance with the
Purchase Agreement. Further, King is obligated to offer
employment to certain AVINZA product line employees.
In connection with the Transaction, King has committed to loan
the Company, at the Companys option, $37.8 million
(the Loan) to be used to pay the Companys
co-promote termination obligation to Organon due
October 15, 2006. This loan was drawn, and the
$37.8 million co-promote liability settled in October 2006.
Amounts due under the loan are subject to certain market terms,
including a 9.5% interest rate and a security interest in
Company assets other than those related to AVINZA. Upon Closing,
accrued interest on the Loan will be forgiven and the amount of
the Closing Payment will be increased by the amount of the loan,
including interest thereon, if any, and an equal amount will be
credited against that payment for repayment of the loan. If the
Closing does not occur, accrued interest and the outstanding
principal amount due thereunder would become due on
January 1, 2007.
The Purchase Agreement may be terminated by either King or the
Company if the Closing has not occurred by December 31,
2006, or upon the occurrence of certain customary matters. In
addition, if the Purchase Agreement is terminated under certain
circumstances, including a determination by the Companys
board of directors to accept an acquisition proposal it deems
superior to the Transaction, the Company has agreed to pay King
a termination fee of $12.0 million. The Closing is subject
to certain closing conditions, including, but not limited to,
Company stockholder approval of the Transaction, the conversion
or redemption prior to Closing of all outstanding
6% Convertible Subordinated Notes due 2007 of the Company,
the expiration of the waiting period under the
Hart-Scott-Rodino
Antitrust Improvements Act of 1976, as amended, and certain
other customary closing conditions.
74
AVINZA
PRODUCT LINE OF LIGAND PHARMACEUTICALS INCORPORATED
NOTES TO
FINANCIAL STATEMENTS (Continued)
Also on September 6, 2006, the Company entered into a
Contract Sales Force Agreement (the Sales Agreement)
with King, pursuant to which King agreed to conduct a detailing
program (the Detailing Program) to promote the sale
of AVINZA for an agreed upon fee, subject to the terms and
conditions of the Sales Agreement. Pursuant to the Sales
Agreement, King has agreed to perform certain minimum monthly
product details (i.e. sales calls), which commenced effective
October 1, 2006 and will continue for a period of six
months following such date or until the Closing or earlier
termination of the Purchase Agreement. The Company estimates
that, assuming the Closing were to occur at the end of December
2006, the amount due to King under the Sales Agreement would be
approximately $4.0 million.
75
PROPOSAL TWO:
AMENDMENT
TO STOCK 2002 STOCK INCENTIVE PLAN
You are being asked to approve an amendment to Ligands
2002 Stock Incentive Plan (the 2002 Plan) to permit
adjustment of outstanding options in the event of a special cash
dividend that affects the common stock or share price of the
common stock underlying the options in an equitable manner. If
the proposed amendment is approved Ligand will be able to adjust
the outstanding options issued under the 2002 Plan to reflect
the payment of a special cash dividend to our stockholders after
the consummation of the asset sale. Such adjustments may take
the form of either an adjustment to each outstanding
options strike price
and/or the
number of shares granted under such option in order to equitably
reflect the amount of cash distributed to our stockholders as a
cash dividend.
The following is a summary of the principal features of the 2002
Plan. The summary, however, is not a complete description of all
the provisions of the 2002 Plan. Copies of the actual plan
document may be obtained by any stockholder upon written request
to the Corporate Secretary at Ligands principal executive
offices in San Diego, California.
Plan
Structure
The 2002 Plan contains four separate equity programs:
|
|
|
|
|
the Discretionary Option Grant Program,
|
|
|
|
the Automatic Option Grant Program,
|
|
|
|
the Stock Issuance Program, and
|
|
|
|
the Director Fee Option Grant Program.
|
The principal features of these programs are described below.
The 2002 Plan is administered by the compensation committee of
the board. This committee has complete discretion, subject to
the provisions of the 2002 Plan, to authorize option grants and
direct stock issuances under the 2002 Plan. However, the board
may also appoint a secondary committee of one or more members of
our board of directors to have separate but concurrent authority
to make option grants and stock issuances under those programs
to all eligible individuals other than Ligands executive
officers and non-employee members of our board of directors. The
term Plan Administrator, as used in this proxy
statement, will mean either the compensation committee or any
secondary committee, to the extent each such entity is acting
within the scope of its duties under the 2002 Plan. The Plan
Administrator does not exercise any administrative discretion
under the Automatic Option Grant or Director Fee Option Grant
Program for the non-employee members of our board of directors.
All grants under those programs are made in strict compliance
with the express provisions of each such program.
Issuable
Shares
Since its adoption, a total of 9,075,529 shares of common
stock have been reserved for issuance under the 2002 Plan
(including shares transferred from Ligands 1992 Stock
Option/Stock Issuance Plan). As of October 31, 2006,
options for 6,540,899 shares of common stock were
outstanding under the 2002 Plan, 574,974 shares remained
available for future option grant or direct issuance, and
1,944,090 shares have been issued under the 2002 Plan.
In no event may any one participant in the 2002 Plan receive
options, separately exercisable stock appreciation rights and
direct stock issuances for more than one million shares in
any calendar year. If an option expires or is terminated for any
reason before all its shares are exercised, the shares not
exercised will be available for subsequent option grants or
stock issuances under the 2002 Plan. In addition, unvested
shares issued under the 2002 Plan and subsequently repurchased
by Ligand at a price not greater than the original exercise
price or issue price paid per share will be added back to the
number of shares of common stock reserved for issuance under the
2002 Plan. Accordingly, such repurchased shares will be
available for reissuance through one or more subsequent option
grants or direct stock issuances under the 2002 Plan. However,
shares subject to any option surrendered or canceled in
accordance with the stock appreciation right provisions of the
2002 Plan will reduce on a
share-for-share
basis the number of shares of common stock available for
subsequent grants.
76
Adjustments
Should any change be made to the common stock issuable under the
2002 Plan by reason of any stock split, stock dividend,
recapitalization, combination of shares, exchange of shares or
other change affecting the outstanding common stock as a class
without Ligands receipt of consideration, then appropriate
adjustments will be made to:
|
|
|
|
|
the maximum number
and/or class
of securities issuable under the 2002 Plan;
|
|
|
|
the number
and/or class
of securities for which any one person may be granted options,
separately exercisable stock appreciation rights and direct
stock issuances per calendar year under the 2002 Plan;
|
|
|
|
the number
and/or class
of securities for which grants are to be made under the
Automatic Option Grant Program to new or continuing non-employee
members of our board of directors; the number
and/or class
of securities and price per share in effect under each
outstanding option; and
|
|
|
|
the number
and/or class
of securities and the exercise price per share in effect under
each outstanding option under the 2002 Plan.
|
Such adjustments to the outstanding options will be effected in
a manner which will preclude the enlargement or dilution of
rights and benefits under those options. As a result of the plan
modification, any such adjustments to the terms of outstanding
options would be considered a modification for accounting
purposes and result in the recognition of compensation expense
in the Companys consolidated statement of operations under
the requirements of Statement of Financial Accounting Standard
No 123(R) Share-Based Payment
(SFAS 123(R)). Any such expense could be
material.
Eligibility
Officers and employees of Ligand and its subsidiaries, whether
now existing or subsequently established, non-employee members
of our board of directors and consultants and independent
contractors of Ligand and its parent and subsidiaries are
eligible to participate in the 2002 Plan.
As of October 31, 2006, approximately 407 employees and
directors, including 12 executive officers, and
10 non-employee members of our board of directors were
eligible to participate in the Discretionary Option Grant and
Stock Issuance Programs. The 10 non-employee members of our
board of directors were also eligible to participate in the
Automatic Option Grant Program and the Director Fee Option Grant
Program.
Valuation
The fair market value per share of common stock on any relevant
date under the 2002 Plan will be deemed to be equal to the
closing selling price per share on that date on the Nasdaq
National Market. If there is no reported selling price for such
date, then the fair market value per share will be the closing
selling price on the last preceding date for which such
quotation exists.
On ,
2006, the closing selling price per share was
$ .
Discretionary
Grant Program
Grants
The Plan Administrator has complete discretion under the
Discretionary Option Grant Program to determine which eligible
individuals are to receive option grants, the time or times when
those grants are to be made, the number of shares subject to
each such grant, the status of any granted option as either an
incentive stock option or a non-statutory option under the
federal tax laws, the vesting schedule (if any) to be in effect
for the option grant and the maximum term (up to 10 years)
for which any granted option is to remain outstanding.
Price and
Exercisability
Each granted option will have an exercise price per share not
less than 100% of the fair market value per share of common
stock on the option grant date, and no granted option will have
a term in excess of 10 years. The shares subject to each
option will generally become exercisable for fully-vested shares
in a series of installments over a
77
specified period of service measured from the grant date.
However, one or more options may be structured so that they are
immediately exercisable for any or all of the option shares. The
shares acquired under such immediately-exercisable options will
normally be unvested and subject to repurchase by Ligand, at the
lower of (i) the exercise price paid per share or
(ii) the fair market value per share of common stock at the
time of cessation of service if the optionee ceases service with
Ligand prior to vesting in those shares.
The exercise price may be paid in cash or in shares of common
stock. Outstanding options may also be exercised through a
same-day sale program pursuant to which a designated brokerage
firm is to effect an immediate sale of the shares purchased
under the option and pay to Ligand, out of the sale proceeds
available on the settlement date, sufficient funds to cover the
exercise price for the purchased shares plus all applicable
withholding taxes.
No optionee has any stockholder rights with respect to the
option shares until such optionee has exercised the option and
paid the exercise price for the purchased shares. Options are
generally not assignable or transferable other than by will or
the laws of inheritance and, during the optionees
lifetime, the option may be exercised only by such optionee.
However, the Plan Administrator may allow non-statutory options
to be transferred or assigned during the optionees
lifetime to one or more members of the optionees immediate
family or to a trust established exclusively for one or more
such family members or to the optionees former spouse, to
the extent such transfer or assignment is in furtherance of the
optionees estate plan or pursuant to a domestic relations
order. The optionee may also designate one or more beneficiaries
to automatically receive his or her outstanding options at death.
Termination
of Service
Upon cessation of service, the optionee will have a limited
period of time in which to exercise his or her outstanding
options for any shares in which the optionee is vested at that
time. The Plan Administrator has discretion to extend the period
following the optionees cessation of service during which
his or her outstanding options may be exercised, up to the date
of the options expiration
and/or to
accelerate the exercisability or vesting of such options in
whole or in part.
Stock
Issuance Program
Shares may be sold under the Stock Issuance Program at a price
per share not less than their fair market value, payable in
cash. Shares may also be issued as a bonus for past services
without any cash outlay required of the recipient. Shares of
common stock may also be issued under the Stock Issuance Program
pursuant to share right awards which entitle the recipients to
receive those shares upon the attainment of designated
performance goals or completion of a specified service period.
The Plan Administrator has complete discretion under this
program to determine which eligible individuals are to receive
such stock issuances or share right awards, the time or times
when such issuances or awards are to be made, the number of
shares subject to each such issuance or award and the vesting
schedule to be in effect for the stock issuance or share rights
award.
The shares issued may be fully and immediately vested upon
issuance or may vest upon the recipients completion of a
designated service period or upon Ligands attainment of
pre-established performance goals. The Plan Administrator has,
however, the discretionary authority at any time to accelerate
the vesting of any and all unvested shares outstanding under the
Stock Issuance Program.
Any unvested shares for which the requisite service requirement
or performance objective is not obtained must be surrendered to
Ligand for cancellation, and the participant will not have any
further stockholder rights with respect to those shares. Ligand
will, however, repay the participant the lower of (i) the
cash amount paid for the surrendered shares or (ii) the
fair market value of those shares at the time of the
participants cessation of service.
Outstanding share right awards under the Stock Issuance Program
will automatically terminate, and no shares of common stock will
actually be issued in satisfaction of those awards, if the
performance goals established for such awards are not attained.
The Plan Administrator, however, has the discretionary authority
to issue shares of common stock in satisfaction of one or more
outstanding share right awards as to which the designated
performance goals are not attained.
78
Automatic
Option Grant Program
Grants
Under the Automatic Option Grant Program, eligible non-employee
members of our board of directors receive a series of option
grants over their period of board service. Each individual who
first becomes a non-employee board member at any time on or
after the effective date receives an option grant for
20,000 shares of common stock on the date such individual
joins the board, provided such individual has not been in the
prior employ of Ligand. In addition, on the date of each annual
stockholders meeting held after the effective date, each
non-employee board member who is to continue to serve as a
non-employee board member (including individuals who joined the
board prior to the effective date) is automatically granted an
option to purchase 10,000 shares of common stock, provided
such individual has served on the board for at least six months.
There is no limit on the number of such
10,000-share
option grants any one eligible non-employee board member may
receive over his or her period of continued board service, and
non-employee members of our board of directors who have
previously been in Ligands employ are eligible to receive
one or more such annual option grants over their period of board
service.
Option
Terms
Each automatic grant has an exercise price per share equal to
the fair market value per share of common stock on the grant
date and has a maximum term of 10 years. The shares subject
to each automatic option grant (whether the initial grant or an
annual grant) fully vest and become exercisable upon the
completion of one year of board service measured from the grant
date. Additionally, the shares subject to each automatic option
grant immediately vest in full upon certain changes in control
or ownership of Ligand or upon the optionees death or
disability while a board member. Each option granted under the
program remains exercisable for vested shares until the earlier
of (i) the expiration of the
10-year
option term or (ii) the expiration of the
3-year
period measured from the date of the optionees cessation
of board service.
Director
Fee Option Grant Program
The Director Fee Option Grant Program is implemented for each
calendar year until otherwise determined by the Plan
Administrator. Under the Director Fee Option Grant Program, each
non-employee board member may elect, prior to the start of each
calendar year, to apply all or any portion of the annual fees
otherwise payable in cash for his or her period of service on
the board for that year to the acquisition of a special
discounted option grant. The option grant is a non-statutory
option under the federal tax laws and is automatically made on
the first trading day in January in the calendar year for which
the director fee election is in effect. The option has a maximum
term of 10 years measured from the grant date and an
exercise price per share equal to one-third of the fair market
value of the option shares on such date. The number of shares
subject to each option is determined by dividing the amount of
the annual fees applied to the acquisition of that option by
two-thirds of the fair market value per share of common stock on
the grant date. As a result, the total spread on the option (the
fair market value of the option shares on the grant date less
the aggregate exercise price payable for those shares) is equal
to the portion of the annual fees applied to the acquisition of
the option. The dollar amount of the fee subject to the board
members election each year is equal to his or her annual
retainer fee, plus the number of regularly-scheduled board
meetings for that year multiplied by the per board meeting fee
in effect for such year. Under the 2002 Plan, the current annual
dollar amount of the fee that can be applied is $27,500 for each
non-employee director, plus $5,000 for the Audit Committee chair
or $2,500 for the compensation committee chair.
The option is exercisable in a series of 12 successive
equal monthly installments upon the optionees completion
of each month of board service in the calendar year for which
the fee election is in effect, subject to full and immediate
acceleration upon certain changes in control or ownership of
Ligand or upon the optionees death or disability while a
board member. Each option granted under the program remains
exercisable for vested shares until the earlier of (i) the
expiration of the
10-year
option term or (ii) the expiration of the
3-year
period measured from the date of the optionees cessation
of board service.
79
General
Plan Provisions
Valuation
For all valuation purposes under the 2002 Plan, the fair market
value per share of common stock on any date is deemed equal to
the closing selling price per share on that date, as reported on
the Nasdaq Global Market. If there is no reported selling price
for such date, then the fair market value per share is the
closing selling price on the last preceding date for which such
quotation exists.
On ,
2006, the closing selling price per share was
$ .
Vesting
Acceleration
In the event that Ligand is acquired by merger or asset sale, or
if there is a change in ownership or control, then options
granted under the Discretionary Option Grant Program may:
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vest or accelerate in full when such options are not to be
assumed by any successor corporation;
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vest in full when such options are to be assumed by any
successor corporation; or
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vest or accelerate in full when such options are to be assumed
by any successor corporation and the employee holding such
options is involuntarily terminated.
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The shares subject to each option under the Automatic Option
Grant and Director Fee Option Grant Programs immediately vest
upon (i) an acquisition of Ligand by merger or asset sale,
(ii) the successful completion of a tender offer for more
than 50% of Ligands outstanding voting stock or
(iii) a change in the majority of the board effected
through one or more contested elections for members of our board
of directorship.
The acceleration of vesting in the event of a change in the
ownership or control of Ligand may be seen as an anti-takeover
provision and may have the effect of discouraging a merger
proposal, a takeover attempt or other efforts to gain control of
Ligand.
Stock
Appreciation Rights
The Plan Administrator is authorized to issue two types of stock
appreciation rights in connection with option grants made under
the Plan:
Tandem stock appreciation rights, which may be granted
under the Discretionary Option Grant Program, provide the
holders with the right to surrender their options for an
appreciation distribution from Ligand equal in amount to the
excess of (a) the fair market value of the vested shares of
common stock subject to the surrendered option over (b) the
aggregate exercise price payable for those shares. Such
appreciation distribution may, at the discretion of the Plan
Administrator, be made in cash or in shares of common stock.
Limited stock appreciation rights may be granted under
the Discretionary Option Grant Program to one or more officers
of Ligand as part of their option grants, and such rights will
automatically be included as part of each grant made under the
Automatic Option Grant and Director Fee Option Grant Programs.
Options with such a limited stock appreciation right may be
surrendered to Ligand upon the successful completion of a
hostile tender offer for more than 50% of Ligands
outstanding voting stock. In return for the surrendered option,
the optionee will be entitled to a cash distribution from Ligand
in an amount per surrendered option share equal to the excess of
(a) the highest price per share of common stock paid in
connection with the tender offer over (b) the exercise
price payable for such share.
Special
Tax Election
The Plan Administrator may provide one or more holders of
options or unvested share issuances under the 2002 Plan with the
right to have Ligand withhold a portion of the shares otherwise
issuable to such individuals in satisfaction of the withholding
taxes to which such individuals may become subject in connection
with the exercise of those options or the vesting of those
shares. Alternatively, the Plan Administrator may allow such
individuals to deliver previously acquired shares of common
stock in payment of such withholding tax liability.
80
Amendment
and Termination
The board may amend or modify the 2002 Plan at any time, subject
to any required stockholder approval pursuant to applicable laws
and regulations. Unless sooner terminated by the board, the 2002
Plan will terminate on the earlier of:
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March 7, 2012; or
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the termination of all outstanding options in connection with
certain changes in control or ownership of the company.
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Federal
Income Tax Consequences
Option
Grants
Options granted under the 2002 Plan may be either incentive
stock options which satisfy the requirements of Section 422
of the Internal Revenue Code (the Code) or
non-statutory options which are not intended to meet such
requirements. The Federal income tax treatment for the two types
of options differs as follows:
Incentive Options. The optionee recognizes no
taxable income at the time of the option grant, and no taxable
income is generally recognized at the time the option is
exercised. However, the amount by which the fair market value
(at the time of exercise) of the purchased shares exceeds the
exercise price will be included in the optionees income
for purposes of the alternative minimum tax. The optionee will,
however, recognize taxable income in the year in which the
purchased shares are sold or otherwise made the subject of a
taxable disposition. For Federal tax purposes, dispositions are
divided into two categories: (i) qualifying and
(ii) disqualifying. A qualifying disposition occurs if the
sale or other disposition is made after the optionee has held
the shares for more than two years after the option grant date
and more than one year after the exercise date. If either of
these two holding periods is not satisfied, then a disqualifying
disposition will result.
Upon a qualifying disposition, the optionee will recognize
long-term capital gain in an amount equal to the excess of
(i) the amount realized upon the sale or other disposition
of the purchased shares over (ii) the exercise price paid
for the shares. If there is a disqualifying disposition of the
shares, then the excess of (i) the lesser of the fair
market value of those shares on the exercise date or the sale
date over (ii) the exercise price paid for the shares will
be taxable as ordinary income to the optionee. Any additional
gain or loss recognized upon the disposition will be recognized
as a capital gain or loss by the optionee.
If the optionee makes a disqualifying disposition of the
purchased shares, then Ligand will be entitled to an income tax
deduction, for the taxable year in which such disposition
occurs, equal to the excess of (i) the fair market value of
such shares on the option exercise date or the sale date, if
less, over (ii) the exercise price paid for the shares. In
no other instance will Ligand be allowed a deduction with
respect to the optionees disposition of the purchased
shares.
Non-Statutory Options. No taxable income is
recognized by an optionee upon the grant of a non-statutory
option. The optionee will in general recognize ordinary income
in the year in which the option is exercised, equal to the
excess of the fair market value of the purchased shares on the
exercise date over the exercise price paid for the shares, and
the optionee will be required to satisfy the tax withholding
requirements applicable to such income.
If the shares acquired upon exercise of the non-statutory option
are unvested and subject to repurchase by Ligand in the event of
the optionees termination of service prior to vesting in
those shares, then the optionee will not recognize any taxable
income at the time of exercise but will have to report as
ordinary income, as and when Ligands repurchase right
lapses, an amount equal to the excess of (i) the fair
market value of the shares on the date the repurchase right
lapses over (ii) the exercise price paid for the shares.
The optionee may, however, elect under Section 83(b) of the
Internal Revenue Code to include as ordinary income in the year
of exercise of the option an amount equal to the excess of
(i) the fair market value of the purchased shares on the
exercise date over (ii) the exercise price paid for such
shares. If the Section 83(b) election is made, the optionee
will not recognize any additional income as and when the
repurchase right lapses.
81
Ligand is entitled to an income tax deduction equal to the
amount of ordinary income recognized by the optionee with
respect to the exercised non-statutory option. The deduction is
in general allowed for the taxable year of Ligand in which such
ordinary income is recognized by the optionee.
Stock
Appreciation Rights
No taxable income is recognized upon receipt of a stock
appreciation right. The holder recognizes ordinary income, in
the year in which the stock appreciation right is exercised, in
an amount equal to the excess of the fair market value of the
underlying shares of common stock on the exercise date over the
base price in effect for the exercised right, and the holder is
required to satisfy the tax withholding requirements applicable
to such income.
Ligand is entitled to an income tax deduction equal to the
amount of ordinary income recognized by the holder in connection
with the exercise of the stock appreciation right. The deduction
generally is allowed for the taxable year in which such ordinary
income is recognized.
Direct
Stock Issuance
The tax principles applicable to direct stock issuances under
the stock plan are substantially the same as those summarized
above for the exercise of non-statutory option grants.
Deductibility
of Executive Compensation
Ligand believes that any compensation deemed paid by it in
connection with disqualifying dispositions of incentive stock
option shares or exercises of non-statutory options under the
Discretionary Option Grant or Automatic Option Grant Programs
qualifies as performance-based compensation for purposes of Code
Section 162(m) and does not have to be taken into account
for purposes of the $1 million limitation per covered
individual on the deductibility of the compensation paid to
certain executive officers of Ligand. Accordingly, all
compensation deemed paid with respect to those options remains
deductible by Ligand without limitation under Code
Section 162(m). Option grants under the Director Fee Option
Grant Program do not qualify as performance-based compensation,
and any income tax deductions attributable to the exercise of
those options are subject to the $1 million limitation.
Amendment
The proposed amendment would allow for equitable adjustments to
be made to outstanding options of the type described in the
section above captioned Plan Structure
Adjustments, in the event a large non-recurring
cash dividend is paid to our stockholders, which affects the
common stock or share price of the common stock underlying the
options subject to the 2002 plan.
Stockholder
Approval
The affirmative vote of a majority of the outstanding voting
shares of Ligand present or represented by proxy and entitled to
vote at the annual meeting is required for approval of the
amendment to the 2002 Plan.
Recommendation
of the Board of Directors
The board of directors believes that the amendment of the 2002
Plan is necessary in order to retain the services of, and
equitably treat, individuals who received options under the 2002
Plan in the event of a large non-recurring cash dividend is paid
in connection with the proposed asset sale. THE BOARD OF
DIRECTORS UNANIMOUSLY RECOMMENDS A VOTE FOR THE AMENDMENT.
82
Stock &
Options Awards to Officers & Directors
The table below shows, as to our chief executive and each of the
next four most highly-compensated executive officers, which
includes each individual listed in the table below (the
Named Executive Officers), and the various indicated
individuals and groups, the number of shares of common stock
subject to options granted under the 2002 Plan during 2005 and
through October 31, 2006, together with the weighted
exercise price payable per share.
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Weighted Average
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Options Granted
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Exercise Price of
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Name and Principal Position
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(Number of Shares)
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Granted Options ($)
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David E. Robinson(1)
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150,000
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$
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8.80
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Former Chairman of the Board,
President,
Chief Executive Officer and Director
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Henry F.
Blissenbach(2)
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172,009
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$
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9.3745
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Chairman of the Board and
Interim Chief Executive Officer
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Andres F. Negro-Vilar
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60,000
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$
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9.1875
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Executive Vice President, Research
and Development and Chief Scientific Officer
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Paul V. Maier
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55,000
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$
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8.9409
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Senior Vice President, Chief
Financial Officer
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Warner R. Broaddus
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45,000
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$
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9.8333
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Vice President, General Counsel
and Secretary
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Tod G. Mertes
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35,000
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$
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9.9071
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Vice President, Controller and
Treasurer
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All directors who are not
executive officers (10 persons)
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219,707
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$
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10.4849
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All current executive officers as
a group (10 persons)(1)
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622,009
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$
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8.9859
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All employees who are not
executive officers (507 persons)(1)
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1,346,594
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$
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9.8336
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(1) |
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On July 31, 2006, Mr. Robinson resigned as director,
Chairman, President and Chief Executive Officer. For purposes of
this table, Mr. Robinson is not treated as a current
executive officer, but is included in the employee total. |
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(2) |
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On August 1, 2006, our board of directors appointed
Dr. Blissenbach Chairman and Interim Chief Executive
Officer. |
New Plan
Benefits
Each of the non-employee members of our board of directors will,
upon his re-election to the board at the next annual meeting of
stockholders, receive an option grant under the 2002 Plans
Automatic Option Grant Program for 10,000 shares of common
stock, namely Mr. Areyh, Dr. Cross, Dr. Johnson,
Dr. Kozarich, Mr. Loeb, Dr. Peck,
Dr. Roberts and Mr. Rocca. Each option will have an
exercise price per share equal to the fair market value per
share of common stock on the grant date.
Compensation
Plans
We have two compensation plans approved by our stockholders
under which our equity securities are authorized for issuance to
employees and directors for goods or services. The 2002 Stock
Option/Stock Issuance Plan (effective May 16,
2002) which is the successor plan to Ligands 1992
Stock Option/Stock Issuance Plan; and the 2002 Employee Stock
Purchase Plan (effective July 1, 2002) which is the
successor plan to Ligands 1992 Employee Stock Purchase
Plan.
83
The following table summarizes information about our equity
compensation plans as of December 31, 2005:
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(c)
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Number of
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(a)
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securities
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Number of
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remaining available
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securities to be
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(b)
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for future issuance
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issued upon
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Weighted-average
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under equity
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exercises of
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exercise price of
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compensation plans
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outstanding
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outstanding
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(excluding
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options, warrants
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options, warrants
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securities
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and rights
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and rights
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reflected in column(a))
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Equity compensation plans approved
by security holders
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7,001,657
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11.76
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202,424
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(1)
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Equity compensation plans not
approved by security holders(2)
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7,001,657
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11.76
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202,424
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(1) |
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At December 31, 2005, 54,914 and 147,510 shares were
available under the 2002 Option Plan and the 2002 Employee Stock
Purchase Plan, respectively for future grants of stock options
or sale of stock. On January 31, 2006, shareholders of the
Company approved an amendment to the 2002 Plan to increase the
number of shares of the Companys common stock authorized
for issuance by 750,000 shares, from 8.3 million
shares to 9.1 million shares. |
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(2) |
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There are no equity compensation plans (including individual
compensation arrangements) not approved by the Companys
security holders. |
84
EXECUTIVE
COMPENSATION
The following table summarizes the compensation earned by our
chief executive and the next four most highly-compensated
executive officers, which includes each individual listed in the
table below (the Named Executive Officers), for
services rendered in all capacities to Ligand and its
subsidiaries for the fiscal years ended December 31, 2005,
2004, and 2003:
SUMMARY
COMPENSATION TABLE
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Long-Term
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Compensation
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Awards
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Annual Compensation
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Securities
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Other Annual
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Underlying
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All Other
|
Name and Principal Position
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Year
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Salary ($)(1)
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Bonus ($)
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Compensation ($)(2)
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Options/ SARs (#)
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Compensation ($)(3)
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David E. Robinson(4)
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2005
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666,667
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150,000
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6,080
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100,000
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|
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2,322
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|
Chairman of the Board,
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2004
|
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643,333
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188,049
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150,000
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2,322
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President and CEO
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2003
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623,333
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250,000
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|
|
|
334,966
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|
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|
175,000
|
|
|
|
2,322
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Andres F. Negro-Vilar
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2005
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|
450,000
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|
|
|
125,000
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|
|
|
135,949
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|
|
|
35,000
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|
|
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6,858
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|
Executive Vice President,
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2004
|
|
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|
423,800
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|
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|
70,000
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|
|
|
142,987
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|
|
|
30,000
|
|
|
|
3,564
|
|
Research and Development and
|
|
|
2003
|
|
|
|
407,500
|
|
|
|
91,750
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|
|
|
211,352
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|
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75,000
|
|
|
|
3,564
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|
Chief Scientific Officer
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|
|
|
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|
|
|
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|
|
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|
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Paul V. Maier
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|
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2005
|
|
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|
335,000
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|
|
|
51,000
|
|
|
|
25,325
|
|
|
|
35,000
|
|
|
|
2,322
|
|
Senior Vice President,
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|
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2004
|
|
|
|
304,750
|
|
|
|
|
|
|
|
31,665
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|
|
|
30,000
|
|
|
|
2,322
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|
Chief Financial Officer
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2003
|
|
|
|
287,500
|
|
|
|
63,250
|
|
|
|
54,268
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|
|
|
75,000
|
|
|
|
2,322
|
|
Warner R. Broaddus
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|
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2005
|
|
|
|
286,000
|
|
|
|
58,000
|
|
|
|
|
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|
|
20,000
|
|
|
|
526
|
|
Vice President, General
|
|
|
2004
|
|
|
|
238,140
|
|
|
|
35,000
|
|
|
|
|
|
|
|
20,000
|
|
|
|
493
|
|
Counsel and Secretary
|
|
|
2003
|
|
|
|
220,500
|
|
|
|
44,100
|
|
|
|
|
|
|
|
25,000
|
|
|
|
461
|
|
Tod G. Mertes
|
|
|
2005
|
|
|
|
240,000
|
|
|
|
108,000
|
|
|
|
|
|
|
|
15,000
|
|
|
|
468
|
|
Vice President, Controller
|
|
|
2004
|
|
|
|
200,000
|
|
|
|
30,000
|
|
|
|
|
|
|
|
20,000
|
|
|
|
381
|
|
and Treasurer
|
|
|
2003
|
|
|
|
158,151
|
|
|
|
40,000
|
|
|
|
|
|
|
|
37,500
|
|
|
|
283
|
|
|
|
|
(1) |
|
Compensation deferred at the election of the executive, pursuant
to the Ligand Pharmaceuticals 401(k) Plan and Ligand Deferred
Compensation Plan are included in the year earned. |
|
(2) |
|
Amounts represent the value of excess earnings on contributions
to the Deferred Compensation Plan that were either paid or for
which payment was deferred at the election of the officer.
Messrs. Broaddus and Mertes did not participate in the
Compensation Plan for each of the periods. |
|
(3) |
|
Amounts represent the value of life insurance premiums. |
|
(4) |
|
Mr. Robinson resigned as director, Chairman, President and
Chief Executive Officer of the Company on July 31, 2006. On
August 1, 2006, the Company named Henry F. Blissenbach, one
of our directors, as Chairman and Interim Chief Executive
Officer. |
85
Stock
Awards.
The following table provides information on the option grants
made to the Named Executive Officers during the fiscal year
ended December 31, 2005. For all employees (including the
executive officers, but excluding the non-employee directors),
options to purchase a total of 951,382 shares of stock were
granted during the same fiscal year. No stock appreciation
rights were granted to the Named Executive Officers during that
fiscal year.
OPTION/SAR
GRANTS IN LAST FISCAL YEAR
INDIVIDUAL GRANTS
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Potential Realizable
|
|
|
|
Number of
|
|
|
% of Total
|
|
|
|
|
|
|
|
|
Value at Assumed Annual
|
|
|
|
Securities
|
|
|
Options/SARs
|
|
|
Exercise
|
|
|
|
|
|
Rates of Stock Price
|
|
|
|
Underlying
|
|
|
Granted to
|
|
|
or
|
|
|
|
|
|
Appreciation for
|
|
|
|
Options/SARs
|
|
|
Employees in
|
|
|
Base Price
|
|
|
Expiration
|
|
|
Option Term
|
|
Name
|
|
Granted (#)
|
|
|
Fiscal Year
|
|
|
($/Sh)
|
|
|
Date
|
|
|
5% ($)
|
|
|
10% ($)
|
|
|
David E. Robinson
|
|
|
100,000
|
|
|
|
10.5110
|
|
|
|
7.25
|
|
|
|
7/5/15
|
|
|
|
455,949
|
|
|
|
1,155,463
|
|
Andres F. Negro-Vilar
|
|
|
35,000
|
|
|
|
3.6789
|
|
|
|
7.25
|
|
|
|
7/5/15
|
|
|
|
159,582
|
|
|
|
404,412
|
|
Paul V. Maier
|
|
|
35,000
|
|
|
|
3.6789
|
|
|
|
7.25
|
|
|
|
7/5/15
|
|
|
|
159,582
|
|
|
|
404,412
|
|
Warner R. Broaddus
|
|
|
20,000
|
|
|
|
2.1022
|
|
|
|
7.25
|
|
|
|
7/5/15
|
|
|
|
91,190
|
|
|
|
231,093
|
|
Tod G. Mertes
|
|
|
15,000
|
|
|
|
1.5767
|
|
|
|
7.25
|
|
|
|
7/5/15
|
|
|
|
68,392
|
|
|
|
173,320
|
|
Each option has a maximum term of 10 years measured from
such grant date, subject to earlier termination upon the
optionees cessation of service with Ligand. The shares
subject to each option are only exercisable if vested and will
vest 12.5% upon six months of service after grant and after
that, in 42 monthly installments. The vesting of the shares
subject to the options granted to Mr. Robinson will
accelerate in connection with his termination of employment
under certain circumstances, including a change in control of
Ligand. The shares subject to the options granted to the other
Named Executive Officers will immediately vest in full in the
event their employment were to terminate following certain
changes in control of Ligand. These arrangements are described
below in Employment, Severance and Change of Control
Arrangements with Executive Officers.
The Plan Administrator may grant tandem stock appreciation
rights in connection with option grants which require the holder
to elect between the exercise of the underlying option for
shares of common stock and the surrender of such option for a
distribution from Ligand, payable in cash or shares of common
stock, based upon the appreciated value of the option shares.
The exercise price may be paid in cash, in shares of common
stock valued at fair market value on the exercise date or
through a cashless exercise procedure involving a same-day sale
of the purchased shares. The optionee may be permitted, subject
to the approval of the plan administrator, to apply a portion of
the shares purchased under the option, or to deliver existing
shares of common stock, in satisfaction of such tax liability.
Ligand does not provide assurance to any executive officer or
any other holder of Ligands securities that the actual
stock price appreciation over the
10-year
option term will be at the assumed 5% and 10% levels or at any
other defined level. Unless the market price of the common stock
does in fact appreciate over the option term, no value will be
realized from the option grants made to the executive officers.
86
The following table shows information concerning option
exercises and holdings for the year ended December 31, 2005
with respect to each of the Named Executive Officers. No stock
appreciation rights were exercised by the named Executive
Officers during such fiscal year, and no stock appreciation
rights were held by them at the end of such fiscal year.
AGGREGATED
OPTION EXERCISES IN LAST FISCAL YEAR AND
FISCAL YEAR-END OPTION VALUES
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Number of Securities Underlying
|
|
|
|
|
|
|
|
|
|
Shares
|
|
|
|
|
|
Unexercised Options/SARs at
|
|
|
Value of Unexercised
In-the-Money
|
|
|
|
acquired on
|
|
|
Value
|
|
|
December 31, 2005
|
|
|
Options/SARs at December 31, 2005
|
|
Name
|
|
exercise
|
|
|
realized ($)
|
|
|
Exercisable (#)
|
|
|
Unexercisable (#)
|
|
|
Exercisable ($)
|
|
|
Unexercisable ($)
|
|
|
David E. Robinson
|
|
|
|
|
|
|
|
|
|
|
891,667
|
|
|
|
158,333
|
|
|
|
433,167
|
|
|
|
500,833
|
|
Andres Negro-Vilar
|
|
|
|
|
|
|
|
|
|
|
380,875
|
|
|
|
60,000
|
|
|
|
349,783
|
|
|
|
184,000
|
|
Paul V. Maier
|
|
|
|
|
|
|
|
|
|
|
325,477
|
|
|
|
60,000
|
|
|
|
236,754
|
|
|
|
184,000
|
|
Warner R. Broaddus
|
|
|
|
|
|
|
|
|
|
|
96,667
|
|
|
|
28,333
|
|
|
|
31,667
|
|
|
|
93,833
|
|
Tod G. Mertes
|
|
|
|
|
|
|
|
|
|
|
59,844
|
|
|
|
27,656
|
|
|
|
41,633
|
|
|
|
79,492
|
|
Value realized on exercise is based upon the market price of the
purchased shares on the exercise date less the option exercise
price paid for those shares. Value of unexercised
in-the-money
options is equal to the fair market value of the securities
underlying the option at fiscal
year-end,
$11.15 per share, less the exercise price payable for those
securities.
Employment,
Severance and Change of Control Arrangements with Named
Executive Officers
In July 2006, Ligand entered into a separation agreement with
Mr. Robinson pursuant to which he resigned as Chairman,
President and Chief Executive Officer of Ligand. Under this
agreement Mr. Robinson will continue to receive his base
salary and certain other benefits for twenty-four months,
payable in five monthly installments, which began on
August 1, 2006, and will end on December 1, 2006.
Additionally, all of Mr. Robinsons unvested stock
options and restricted stock immediately vested and became
exercisable, and remain exercisable until January 17, 2007.
In connection with the separation agreement, Mr. Robinson
executed a general release of claims in favor of Ligand.
In September 1996, Ligand entered into an employment agreement
with
Dr. Negro-Vilar
pursuant to which he is employed as Executive Vice President,
Research and Chief Scientific Officer for an unspecified term.
The agreement provides that
Dr. Negro-Vilar
is an
at-will
employee. In the event his employment is terminated without
cause, he will be entitled to 12 months of salary
continuation payments, and all of his outstanding options will
immediately vest and become exercisable for all of the option
shares.
In September 1992, Ligand entered into an employment agreement
with Paul V. Maier pursuant to which Mr. Maier is employed
as Senior Vice President and Chief Financial Officer for an
unspecified term. The agreement provides that Mr. Maier is
an at-will employee. If Mr. Maiers employment is
terminated by Ligand without cause, he will be entitled to
six months base salary.
Additionally, Ligand has entered into employee retention
agreements dated March 1, 2006 with each of
Dr. Negro-Vilar
and Messrs. Maier and Broaddus. The agreements provide for
certain retention or stay bonus payments in cash
and/or stock
options under specified circumstances as an additional incentive
to remain employed in good standing with Ligand.
In December 2005 Ligand entered into an agreement with
Mr. Mertes that provides for certain severance and
retention or stay bonus payments under specified circumstances.
If Mr. Mertes employment is involuntarily terminated
as defined in the agreement, prior to December 31, 2006,
Mr. Mertes is entitled to receive a payment equal to
12 months regular salary. Under the Decmeber 2005
agreement, if Mr. Mertes remains employed and available for
work through December 31, 2006, he is entitled to receive a
stay bonus of four months salary. Mr. Mertes may
receive all or part of the stay bonus if he is involuntarily
terminated in connection with a change of control on or before
December 31, 2006. Subsequently, Ligand entered into a
severance letter agreement with
87
Mr. Mertes in August 2006, which provides for payment of
six months salary in the event that his employment is
terminated without cause, including in the event that there is a
change of control. Additionally, Ligand entered into a severance
and retention letter agreement with Mr. Mertes in October
2006 which provides, notwithstanding the provisions of the
August 2006 agreement, that provided Mr. Mertes remains in
good standing with Ligand through the final filing of the 2006
annual report on
Form 10-K,
he will be entitled to receive (i) the payout of his
severance benefits under the December 2005 agreement mentioned
above and (ii) the payout of any bonus due in accordance
with Ligands 2006 executive bonus plan.
Ligand has entered into an agreement with each employee holding
one or more outstanding options under the 2002 Plan, including
each of the Named Executive Officers other than
Mr. Robinson, pursuant to which such options will
automatically vest on an accelerated basis in the event that
such individuals employment is terminated following:
|
|
|
|
|
an acquisition of Ligand by merger or asset sale or
|
|
|
|
a change in control of Ligand effected through a successful
tender offer for more than 50% of Ligands outstanding
common stock or through a change in the majority of the Board as
a result of one or more contested elections for Board membership.
|
Ligand has entered into severance agreements with each of the
Named Executive Officers and the other executive officers other
than Mr. Robinson pursuant to which such individuals will,
in the event their employment is involuntarily terminated in
connection with a change in control of Ligand, receive a
severance benefit equal to one times the annual rate of base
salary in effect for such officer at the time of involuntary
termination plus one times the average of bonuses paid to such
officer for services rendered in the two fiscal years
immediately preceding the fiscal year of involuntary
termination. If such events occurred, options held by the
officers would be accelerated and their period of exercisability
extended.
Following Mr. Robinsons departure, and beginning in
August 2006, Ligand agreed to pay Dr. Blissenbach
$40,000 per month, subject to cancellation by either
Dr. Blissenbach or Ligand upon 30 days notice,
for his services as Chairman and Interim Chief Executive
Officer. In addition, Dr. Blissenbach will be eligible to
receive incentive compensation of up to $100,000, based upon his
performance of certain objectives. Additionally, he received a
special stock option grant to purchase 150,000 shares of
Ligands common stock at an exercise price equal to the
closing price of Ligands common stock on August 3,
2006, as reported on the Nasdaq Global Market.
Fifty percent of these stock options will vest at the end
of six months and the remaining fifty percent will vest at
the end of one year, except that all options will vest upon
the appointment of a new chief executive officer. Ligand will
also reimburse Dr. Blissenbach for all reasonable expenses
incurred in discharging his duties as interim chief executive
officer, including, but not limited to commuting costs to
San Diego and living and related costs during the time he
spends in San Diego.
Compensation
Committee Interlocks and Insider Participation
Relationships
and Independence of the Compensation Committee Members
During fiscal 2005, the Compensation Committee was composed of
Dr. Blissenbach and Mr. Groom. No member of the
Compensation Committee was at any time during the 2005 fiscal
year or at any other time an officer or employee of Ligand. No
executive officer of Ligand served on the board of directors or
compensation committee of any entity which has one or more
executive officers serving as members of Ligands board of
directors or Compensation Committee. On August 1, 2006,
Dr. Alexander D. Cross replaced Dr. Blissenbach
on the Compensation Committee due to Dr. Blissenbachs
appointment as Chairman and Interim Chief Executive Officer.
SECURITY
OWNERSHIP OF CERTAIN BENEFICIAL OWNERS,
DIRECTORS AND MANAGEMENT
The following table shows, based on information we have, the
beneficial ownership of our common stock as of October 31,
2006, by:
|
|
|
|
|
all persons who are beneficial owners of 5% or more of our
outstanding common stock;
|
88
|
|
|
|
|
each of our current directors, including our Chairman and
Interim Chief Executive Officer, Dr. Blissenbach, our Named
Executive Officers; and
|
|
|
|
all of our Named Executive Officers and directors as a group.
|
Unless otherwise indicated, each of the stockholders has sole
voting and investment power with respect to the shares
beneficially owned, subject to community property laws, where
applicable. Percentage of ownership is based on approximately
79,230,000 shares of common stock outstanding on
October 31, 2006. Shares of common stock underlying options
and convertible notes includes options which are currently
exercisable or will become exercisable and convertible notes
which are currently convertible or will become convertible
within 60 days after October 31, 2006, are deemed
outstanding for computing the percentage of the person or group
holding such options, but are not deemed outstanding for
computing the percentage of any other person or group. The
address for individuals for whom an address is not otherwise
indicated is 10275 Science Center Drive, San Diego, CA
92121.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares Beneficially
|
|
|
|
|
|
|
|
|
|
Owned via Options,
|
|
|
|
|
|
|
Number of Shares
|
|
|
Warrants or
|
|
|
Percent of Class
|
|
Beneficial Owner
|
|
Beneficially Owned
|
|
|
Convertible Notes
|
|
|
Owned
|
|
|
David M. Knott(1)
|
|
|
8,463,557
|
|
|
|
|
|
|
|
10.7
|
%
|
485 Underhill Blvd., Ste. 205
|
|
|
|
|
|
|
|
|
|
|
|
|
Syosset, NY
11791-3419
|
|
|
|
|
|
|
|
|
|
|
|
|
Daniel S. Loeb(2)
|
|
|
7,375,000
|
|
|
|
|
|
|
|
9.31
|
%
|
Third Point LLC
|
|
|
|
|
|
|
|
|
|
|
|
|
390 Park Avenue
|
|
|
|
|
|
|
|
|
|
|
|
|
New York, NY 10022
|
|
|
|
|
|
|
|
|
|
|
|
|
OrbiMed Advisors LLC(3)
|
|
|
7,332,924
|
|
|
|
|
|
|
|
9.26
|
%
|
767 Third Avenue, 30th Floor
|
|
|
|
|
|
|
|
|
|
|
|
|
New York, NY 10017
|
|
|
|
|
|
|
|
|
|
|
|
|
Farallon Capital Management,
L.L.C.(5)
|
|
|
7,267,327
|
|
|
|
|
|
|
|
9.17
|
%
|
One Maritime Plaza, Suite 1325
|
|
|
|
|
|
|
|
|
|
|
|
|
San Francisco, CA 94111
|
|
|
|
|
|
|
|
|
|
|
|
|
Glenview Capital Management LLC(4)
|
|
|
6,906,000
|
|
|
|
|
|
|
|
8.72
|
%
|
399 Park Avenue, Floor 39
|
|
|
|
|
|
|
|
|
|
|
|
|
New York, NY 10022
|
|
|
|
|
|
|
|
|
|
|
|
|
JP Morgan Chase & Co.(6)
|
|
|
5,455,900
|
|
|
|
|
|
|
|
6.89
|
%
|
270 Park Avenue
|
|
|
|
|
|
|
|
|
|
|
|
|
New York, NY 10017
|
|
|
|
|
|
|
|
|
|
|
|
|
Oz Management LLC(7)
|
|
|
4,076,040
|
|
|
|
|
|
|
|
5.14
|
%
|
9 West 57th Street,
39th Floor
|
|
|
|
|
|
|
|
|
|
|
|
|
New York, NY 10019
|
|
|
|
|
|
|
|
|
|
|
|
|
Jason M. Aryeh(10)
|
|
|
1,631,518
|
|
|
|
|
|
|
|
2.06
|
%
|
Henry F. Blissenbach(9)
|
|
|
93,123
|
|
|
|
88,123
|
|
|
|
*
|
|
Alexander D. Cross
|
|
|
120,373
|
|
|
|
81,888
|
|
|
|
*
|
|
John Groom
|
|
|
116,266
|
|
|
|
100,029
|
|
|
|
*
|
|
Irving S. Johnson
|
|
|
106,013
|
|
|
|
83,084
|
|
|
|
*
|
|
John W. Kozarich(8)
|
|
|
43,824
|
|
|
|
36,446
|
|
|
|
*
|
|
Daniel S. Loeb(2)(8)
|
|
|
7,397,378
|
|
|
|
20,000
|
|
|
|
9.34
|
%
|
Carl C. Peck(8)
|
|
|
111,559
|
|
|
|
103,181
|
|
|
|
*
|
|
Jeffrey R. Perry(2)(8)
|
|
|
7,397,378
|
|
|
|
20,000
|
|
|
|
9.34
|
%
|
Brigette Roberts, M.D.(2)(8)
|
|
|
7,397,378
|
|
|
|
20,000
|
|
|
|
9.34
|
%
|
Michael A. Rocca(8)
|
|
|
86,475
|
|
|
|
74,799
|
|
|
|
*
|
|
David E. Robinson(11)
|
|
|
986,925
|
|
|
|
575,000
|
|
|
|
1.25
|
%
|
Andres F. Negro-Vilar
|
|
|
323,942
|
|
|
|
316,709
|
|
|
|
*
|
|
Paul V. Maier
|
|
|
456,533
|
|
|
|
356,810
|
|
|
|
*
|
|
89
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares Beneficially
|
|
|
|
|
|
|
|
|
|
Owned via Options,
|
|
|
|
|
|
|
Number of Shares
|
|
|
Warrants or
|
|
|
Percent of Class
|
|
Beneficial Owner
|
|
Beneficially Owned
|
|
|
Convertible Notes
|
|
|
Owned
|
|
|
Warner R. Broaddus
|
|
|
118,334
|
|
|
|
114,688
|
|
|
|
*
|
|
Tod G. Mertes
|
|
|
80,795
|
|
|
|
78,282
|
|
|
|
*
|
|
Directors and executive officers
as a group (21 persons)(8)
|
|
|
12,307,031
|
|
|
|
2,651,740
|
|
|
|
15.53
|
%
|
|
|
|
* |
|
Less than 1% |
|
(1) |
|
Pursuant to a Schedule 13D/A filed October 27, 2006,
which reported that David M. Knott and Dorset Management
Corporation had sole voting power over 7,693,955 shares,
shared voting power over 678,671 shares, sole dispositive
power over 8,171,973 shares and shared dispositive power
over 291,584 shares. |
|
(2) |
|
Pursuant to a Schedule 13D/A filed December 5, 2005,
which reported that Daniel S. Loeb and Third Point LLC had
shared voting and dispositive power over 7,375,000 shares
and Third Point Offshore Fund, Ltd. had shared voting and
dispositive power over 4,725,800 shares. |
|
(3) |
|
Pursuant to a Schedule 13G/A filed February 10, 2006,
which reported that OrbiMed Advisors LLC had shared voting and
shared dispositive power over 5,613,675 shares; OrbiMed
Capital LLC had shared voting and shared dispositive power over
1,719,249 shares; and Samuel D. Isaly had shared voting and
dispositive power over 7,332,924 shares. |
|
(4) |
|
Pursuant to a Schedule 13G/A filed on February 14,
2006, which reported that Glenview Capital Management, LLC,
Glenview Capital GP, LLC, and Lawrence Robbins had shared voting
and dispositive power over 6,906,000 shares and Glenview
Capital Master Fund, LTD had shared voting and dispositive power
over 3,980,843 shares. |
|
(5) |
|
Pursuant to a Schedule 13D filed September 18, 2006 by
Farallon Capital Management, L.L.C. which reported that Noonday
Asset Management, L.P., Noonday G.P. (U.S.), L.L.C., Noonday
Capital, L.L.C., David I. Cohen, Saurabh K. Mittal, Chun R.
Ding, William F. Duhamel, Richard B. Fried, Monica R. Landry,
William F. Mellin, Stephen L. Millham, Jason E. Moment, Rajiv A.
Patel, Derek C. Schrier, Thomas F. Steyer and Mark C. Wehrly had
shared voting and dispositive power over 7,267,327 shares;
Farallon Partners, L.L.C., had shared voting and dispositive
power over [4,187,416] shares; Farallon Capital Management,
L.L.C., had shared voting and dispositive power over
3,079,911] shares; Farallon Capital Partners, L.P., had
shared voting and dispositive power over 1,316,261 shares;
Farallon Capital Institutional Partners, L.P., had shared voting
and dispositive power over 1,234,108 shares; Farallon
Capital Offshore Investors II, L.P., had shared voting and
dispositive power over 1,228,175 shares; Farallon Capital
Institutional Partners II, L.P., had shared voting and
dispositive power over 172,723 shares; Farallon Capital
Institutional Partners III, L.P., had shared voting and
dispositive power over 138,811 shares, Tinicum Partners,
L.P., had shared voting and dispositive power over
50,988 shares; Noonday Capital Partners, L.L.C., had shared
voting and dispositive power over 28,500 shares; and RR
Capital Partners, L.P., had shared voting and dispositive power
over 17,850 shares. |
|
(6) |
|
Pursuant to a Schedule 13G filed February 10, 2006 by
JP Morgan Chase & Co. which reported sole voting and
dispositive power over 5,455,900 shares. |
|
(7) |
|
Pursuant to a Schedule 13G filed on March 10, 2006,
which reported that Oz Management LLC and Daniel S Och had sole
voting and dispositive power over 4,076,000 shares and Oz
Master Fund, Ltd. had sole voting and dispositive power over
3,830,500 shares. |
|
(8) |
|
Includes restricted stock awards grants under the 2002 Option
Plan. See Director Compensation. |
|
(9) |
|
On August 1, 2006, our board of directors appointed
Dr. Blissenbach Chairman and Interim Executive Officer. |
|
(10) |
|
Includes 1,597,368 shares held by JALAA Equities, LP., of
which Mr. Aryeh is the founder and general partner,
25,330 shares held by Mr. Aryehs spouse and
8,800 held in a family trust. |
|
(11) |
|
On July 31, 2006, Mr. Robinson resigned as director,
Chairman, President and Chief Executive Officer. |
90
PROPOSAL THREE:
ADJOURNMENT
OF THE SPECIAL MEETING
If there are insufficient votes at the time of the special
meeting to approve either proposal one or two, we may propose to
adjourn the special meeting, if a quorum is present, for the
purpose of soliciting additional proxies to approve either
proposal one or two. We currently do not intend to propose
adjournment at the special meeting if there are sufficient votes
to approve the asset sale and adopt the asset purchase
agreement. If the proposal to adjourn the special meeting for
the purpose of soliciting additional proxies is submitted to our
stockholders for approval, such approval of the holders of a
majority of the shares of common stock voting at the special
meeting. Shares that are voted FOR or
AGAINST the proposal will be counted towards the
vote requirement. Neither broker non-votes nor
abstentions are included in the tabulation of the voting results
and, therefore, they do not have the effect of votes against
such proposal.
THE BOARD OF DIRECTORS UNANIMOUSLY RECOMMENDS THAT YOU VOTE
FOR THE ADJOURNMENT OF THE SPECIAL MEETING, IF
NECESSARY, TO SOLICIT ADDITIONAL PROXIES.
91
SOLICITATION
OF PROXIES
In addition to solicitation by mail, our directors, officers and
employees may solicit proxies by telephone, other electronic
means or in person. These people will not receive compensation
for their services, but we will reimburse them for their
out-of-pocket
expenses. We will bear the cost of printing and mailing proxy
materials, including the reasonable expenses of brokerage firms
and others for forwarding the proxy materials to beneficial
owners of common stock.
OTHER
BUSINESS
We are not currently aware of any business to be acted upon at
the special meeting other than the matters discussed in this
proxy statement. Under our bylaws, business transacted at the
special meeting is limited to the purposes stated in the notice
of special meeting, which is provided at the beginning of this
proxy statement. If other matters do properly come before the
special meeting, or at any adjournment or postponement of the
special meeting, we intend that shares of our common stock
represented by properly submitted proxies will be voted in
accordance with the recommendations of our board of directors.
WHERE YOU
CAN OBTAIN ADDITIONAL INFORMATION
Ligand is subject to the informational requirements of the
Securities Exchange Act of 1934, as amended. Ligand files
reports, proxy statements and other information with the SEC.
You may read and copy these reports, proxy statements and other
information at the SECs Public Reference Section at 100 F
Street, N.E., Washington, D.C. 20549. You may obtain
information on the operation of the Public Reference Room by
calling the SEC at
1-800-SEC-0330.
The SEC also maintains an Internet website, located at
http://www.sec.gov, which contains reports, proxy statements and
other information regarding registrants that file electronically
with the SEC.
92
ANNEX A
Asset Purchase Agreement
PURCHASE AGREEMENT
between
LIGAND PHARMACEUTICALS INCORPORATED
and
KING PHARMACEUTICALS, INC.
and
KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC.
Dated as of September 6, 2006
i
TABLE OF
CONTENTS
|
|
|
|
|
|
|
ARTICLE I DEFINITIONS
|
|
|
A-1
|
|
1.1
|
|
Definitions
|
|
|
A-1
|
|
1.2
|
|
Other Definitional Provisions
|
|
|
A-10
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE II
PURCHASE AND SALE
|
|
|
A-10
|
|
2.1
|
|
Transfer of Purchased Assets
|
|
|
A-10
|
|
2.2
|
|
Excluded Assets
|
|
|
A-10
|
|
2.3
|
|
Assumed Liabilities
|
|
|
A-11
|
|
2.4
|
|
Excluded Liabilities
|
|
|
A-11
|
|
2.5
|
|
Seller to Obtain Consent of Third
Parties
|
|
|
A-11
|
|
2.6
|
|
Purchase Price
|
|
|
A-12
|
|
2.7
|
|
Purchase Price Allocation
|
|
|
A-12
|
|
2.8
|
|
Inventory Value Adjustments
|
|
|
A-12
|
|
2.9
|
|
Escrow
|
|
|
A-14
|
|
2.10
|
|
Risk of Loss
|
|
|
A-14
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE III
CLOSING
|
|
|
A-14
|
|
3.1
|
|
Closing
|
|
|
A-14
|
|
3.2
|
|
Transactions at Closing
|
|
|
A-14
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE IV
REPRESENTATIONS AND WARRANTIES OF SELLER
|
|
|
A-15
|
|
4.1
|
|
Organization
|
|
|
A-15
|
|
4.2
|
|
Due Authorization
|
|
|
A-15
|
|
4.3
|
|
No Conflicts; Enforceability
|
|
|
A-15
|
|
4.4
|
|
Title; Assets
|
|
|
A-16
|
|
4.5
|
|
Intellectual Property
|
|
|
A-16
|
|
4.6
|
|
Litigation
|
|
|
A-17
|
|
4.7
|
|
Consents
|
|
|
A-17
|
|
4.8
|
|
Taxes
|
|
|
A-17
|
|
4.9
|
|
Employee Matters
|
|
|
A-17
|
|
4.10
|
|
Compliance with Laws
|
|
|
A-18
|
|
4.11
|
|
Regulatory Matters
|
|
|
A-18
|
|
4.12
|
|
Government Product Contracts;
Liability for Cost and Pricing Data
|
|
|
A-18
|
|
4.13
|
|
Financial Statements
|
|
|
A-19
|
|
4.14
|
|
Warranties
|
|
|
A-19
|
|
4.15
|
|
Brokers, Etc.
|
|
|
A-19
|
|
4.16
|
|
Inventory and Equipment
|
|
|
A-19
|
|
4.17
|
|
Contracts
|
|
|
A-19
|
|
4.18
|
|
Product Liability; Distributors;
Recalls
|
|
|
A-20
|
|
4.19
|
|
Product Treatments; Product
Returns; Exporting and Manufacturing
|
|
|
A-20
|
|
4.20
|
|
Customers, Suppliers and Third
Party Service Providers
|
|
|
A-20
|
|
4.21
|
|
Medical Information
|
|
|
A-20
|
|
4.22
|
|
Disclaimer
|
|
|
A-21
|
|
|
|
|
|
|
|
|
ii
|
|
|
|
|
|
|
ARTICLE V
REPRESENTATIONS AND WARRANTIES OF PURCHASER
|
|
|
A-21
|
|
5.1
|
|
Organization
|
|
|
A-21
|
|
5.2
|
|
Due Authorization
|
|
|
A-21
|
|
5.3
|
|
No Conflicts; Enforceability
|
|
|
A-21
|
|
5.4
|
|
Litigation
|
|
|
A-21
|
|
5.5
|
|
Consents
|
|
|
A-21
|
|
5.6
|
|
Financing
|
|
|
A-22
|
|
5.7
|
|
Brokers, Etc.
|
|
|
A-22
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE VI
COVENANTS PRIOR TO CLOSING
|
|
|
A-22
|
|
6.1
|
|
Access to Information; Reporting;
Correspondence and Notices
|
|
|
A-22
|
|
6.2
|
|
Conduct of the Product Line
Business
|
|
|
A-22
|
|
6.3
|
|
Inventory
|
|
|
A-23
|
|
6.4
|
|
Required Approvals and Consents
|
|
|
A-23
|
|
6.5
|
|
HSR Act
|
|
|
A-24
|
|
6.6
|
|
Proxy Statement; Seller
Stockholders Meeting
|
|
|
A-24
|
|
6.7
|
|
No Negotiation
|
|
|
A-25
|
|
6.8
|
|
Notifications
|
|
|
A-26
|
|
6.9
|
|
Product Packaging
|
|
|
A-26
|
|
6.10
|
|
Further Assurances; Further
Documents
|
|
|
A-26
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE VII
CONDITIONS TO CLOSING
|
|
|
A-26
|
|
7.1
|
|
Conditions Precedent to
Obligations of Purchaser and Seller
|
|
|
A-26
|
|
7.2
|
|
Conditions Precedent to
Purchasers Obligations
|
|
|
A-27
|
|
7.3
|
|
Conditions Precedent to
Sellers Obligations
|
|
|
A-27
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE VIII
ADDITIONAL COVENANTS
|
|
|
A-28
|
|
8.1
|
|
Confidentiality; Publicity
|
|
|
A-28
|
|
8.2
|
|
Availability of Records
|
|
|
A-28
|
|
8.3
|
|
Notification of Customers
|
|
|
A-28
|
|
8.4
|
|
Product Returns, Rebates and
Chargebacks
|
|
|
A-29
|
|
8.5
|
|
Accounts Receivable
|
|
|
A-31
|
|
8.6
|
|
Regulatory Matters
|
|
|
A-31
|
|
8.7
|
|
Website Information
|
|
|
A-32
|
|
8.8
|
|
Tax Matters
|
|
|
A-32
|
|
8.9
|
|
Government Product Contracts
|
|
|
A-32
|
|
8.10
|
|
Insurance
|
|
|
A-32
|
|
8.11
|
|
Product Promotion
|
|
|
A-32
|
|
8.12
|
|
Advisory Fees, etc.
|
|
|
A-33
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE IX
EMPLOYEE MATTERS
|
|
|
A-33
|
|
9.1
|
|
Employee Offers
|
|
|
A-33
|
|
9.2
|
|
Benefits
|
|
|
A-34
|
|
9.3
|
|
WARN Act
|
|
|
A-34
|
|
9.4
|
|
Employee Information
|
|
|
A-34
|
|
|
|
|
|
|
|
|
iii
|
|
|
|
|
|
|
ARTICLE X INDEMNIFICATION
|
|
|
A-34
|
|
10.1
|
|
Indemnification by Seller
|
|
|
A-34
|
|
10.2
|
|
Indemnification by Purchaser
|
|
|
A-35
|
|
10.3
|
|
Procedures
|
|
|
A-35
|
|
10.4
|
|
Certain Limitations on
Indemnification Obligations
|
|
|
A-36
|
|
10.5
|
|
Set-Off
|
|
|
A-36
|
|
10.6
|
|
Survival
|
|
|
A-36
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE XI
TERMINATION AND SURVIVAL
|
|
|
A-36
|
|
11.1
|
|
Termination
|
|
|
A-36
|
|
11.2
|
|
Procedure and Effect of Termination
|
|
|
A-37
|
|
|
|
|
|
|
|
|
|
|
|
|
|
ARTICLE XII
MISCELLANEOUS
|
|
|
A-38
|
|
12.1
|
|
Assignment; Binding Effect
|
|
|
A-38
|
|
12.2
|
|
Expenses
|
|
|
A-38
|
|
12.3
|
|
Notices
|
|
|
A-38
|
|
12.4
|
|
Severability
|
|
|
A-39
|
|
12.5
|
|
Entire Agreement
|
|
|
A-39
|
|
12.6
|
|
No Third Party Beneficiaries
|
|
|
A-39
|
|
12.7
|
|
Waiver
|
|
|
A-39
|
|
12.8
|
|
Governing Law; Jurisdiction
|
|
|
A-39
|
|
12.9
|
|
Injunctive Relief
|
|
|
A-39
|
|
12.10
|
|
Headings
|
|
|
A-40
|
|
12.11
|
|
Counterparts
|
|
|
A-40
|
|
12.12
|
|
Schedules
|
|
|
A-40
|
|
12.13
|
|
Construction
|
|
|
A-40
|
|
iv
LIST
OF EXHIBITS
|
|
|
|
|
Exhibit A
|
|
|
|
Form of Assignment of Product
Intellectual Property
|
Exhibit B
|
|
|
|
Form of Bill of Sale and
Assignment and Assumption Agreement
|
Exhibit C
|
|
|
|
Form of Product License and Supply
Agreement Assignment
|
Exhibit D
|
|
|
|
Form of Second Source Supply
Agreement Assignment
|
Exhibit E
|
|
|
|
Form of Termination and Return of
Rights Agreement Assignment
|
Exhibit F
|
|
|
|
Form of Technical Agreement
Avinza®
Assignment
|
Exhibit G
|
|
|
|
Form of Quality Agreement for
Avinza®
Assignment
|
Exhibit H
|
|
|
|
Form of Transition Services
Agreement
|
Exhibit I
|
|
|
|
Form of Contract Sales Force
Agreement
|
Exhibit J
|
|
|
|
Form of Escrow Agreement
|
Exhibit K
|
|
|
|
Form(s) of Consents to Assignment
|
Exhibit L
|
|
|
|
Product License and Supply
Agreement
|
Exhibit M
|
|
|
|
Second Source Supply Agreement
|
Exhibit N
|
|
|
|
Termination and Return of Rights
Agreement
|
Exhibit O
|
|
|
|
Technical Agreement
Avinza®
|
Exhibit P
|
|
|
|
Quality Agreement for
Avinza®
|
LIST
OF SCHEDULES
|
|
|
|
|
Schedule 1.1(a)
|
|
|
|
Applicable Permits
|
Schedule 1.1(b)
|
|
|
|
Pre-Existing Assigned Contracts
|
Schedule 1.1(c)
|
|
|
|
Inventory
|
Schedule 1.1(d)
|
|
|
|
Knowledge
|
Schedule 1.1(e)
|
|
|
|
Product Domain Names
|
Schedule 1.1(f)
|
|
|
|
Product Equipment
|
Schedule 1.1(g)
|
|
|
|
Product Marks
|
Schedule 1.1(h)
|
|
|
|
Product Trade Dress
|
Schedule 1.1(i)
|
|
|
|
Promotional Materials
|
Schedule 1.1(j)
|
|
|
|
Registrations
|
Schedule 1.1(k)
|
|
|
|
Product Patent Rights
|
Schedule 2.3
|
|
|
|
Assumed Liabilities
|
Schedule 2.5
|
|
|
|
Assigned Contracts
Third Party Consents
|
Schedule 2.6
|
|
|
|
Royalties
|
Schedule 2.7
|
|
|
|
Allocation Schedule
|
Schedule 2.8(b)
|
|
|
|
Inventory Value Adjustments
|
Schedule 3.2(a)(iv)
|
|
|
|
Seller FDA Letter
|
Schedule 3.2(b)(iv)
|
|
|
|
Purchaser FDA Letter
|
Schedule 6.2
|
|
|
|
Conduct of the Product Line
Business
|
Schedule 8.4(a)
|
|
|
|
Product Returns
|
Schedule 8.4(b)
|
|
|
|
Best Price; AMP
|
Schedule 8.4(c)
|
|
|
|
Commercial Rebate Agreements
|
Schedule 9.1(a) (1)
|
|
|
|
Product Employees
|
Schedule 9.1(a) (2)
|
|
|
|
Severance Pay Policy
|
v
SELLER
DISCLOSURE SCHEDULE
|
|
|
|
|
Schedule 4.3
|
|
|
|
No Conflicts
|
Schedule 4.4
|
|
|
|
Title; Assets
|
Schedule 4.5
|
|
|
|
Intellectual Property
|
Schedule 4.6
|
|
|
|
Litigation
|
Schedule 4.7
|
|
|
|
Consents
|
Schedule 4.8
|
|
|
|
Taxes
|
Schedule 4.9
|
|
|
|
Plans and Material Documents
|
Schedule 4.9(g)
|
|
|
|
Product Employee Actions
|
Schedule 4.10
|
|
|
|
Compliance with Laws
|
Schedule 4.11
|
|
|
|
Regulatory Matters
|
Schedule 4.14
|
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Warranties
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Schedule 4.17(a)
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Product Line Business Contracts
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Schedule 4.17(b)
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Contract Deficiencies
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Schedule 4.18
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Product Liability; Distributors;
Recalls
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Schedule 4.19
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Product Treatments; Product
Returns; Exporting and Manufacturing
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vi
PURCHASE
AGREEMENT
THIS PURCHASE AGREEMENT (this
Agreement), dated as of September 6,
2006 (the Execution Date), is entered into by
and between Ligand Pharmaceuticals Incorporated, a Delaware
corporation, and all of its successors and assigns
(Seller), King Pharmaceuticals, Inc., a
Tennessee corporation (King), and King
Pharmaceuticals Research and Development, Inc., a Delaware
corporation and wholly owned subsidiary of King (King
R&D, and together with King,
Purchaser). Each of Seller and Purchaser is
sometimes referred to herein, individually, as a
Party and, collectively, as the
Parties. All capitalized terms used herein
shall have the meanings specified in Article I below
or elsewhere in this Agreement, as applicable.
INTRODUCTION
WHEREAS, subject to the terms and conditions of this Agreement,
Seller desires to transfer all of its rights in and to the
Purchased Assets, including without limitation all of
Sellers rights related to the Distribution (as such
capitalized terms are defined below) of the Product in the
Territory, (collectively, the Product Line
Business) to Purchaser; and
WHEREAS, subject to the terms and conditions of this Agreement,
Seller wishes to sell the Purchased Assets and transfer the
Assumed Liabilities to Purchaser (as such capitalized terms are
defined below), and Purchaser wishes to purchase the Purchased
Assets and assume the Assumed Liabilities from Seller.
NOW, THEREFORE, in consideration of the foregoing and the
representations, warranties, covenants, agreements and
provisions set forth herein and in the Other Agreements, and for
other good and valuable consideration, the receipt and
sufficiency of which are hereby acknowledged, and intending to
be legally bound hereby, the Parties agree as follows:
ARTICLE I
Definitions
Definitions. In addition to the terms defined
above and other terms defined in other Sections of this
Agreement, the following terms shall have the meanings set forth
below for purposes of this Agreement:
Accountants means an accounting firm of
national reputation with pharmaceutical experience (excluding
each of Sellers and Purchasers respective regular
outside accounting firms) as may be mutually acceptable to the
Parties; provided, however, if the Parties are unable to
agree on such accounting firm within ten (10) days or any
such mutually selected accounting firm is unwilling or unable to
serve, then Seller shall deliver to Purchaser a list of three
(3) other accounting firms of national reputation, and
Purchaser shall select one of such three (3) accounting
firms.
Accounts Receivable has the meaning set forth
in Section 2.2(b).
Acquisition Proposal means an unsolicited
proposal from a third party relating to any transaction
involving, in whole or in part, directly or indirectly, the
Product or Product Line Business, including an acquisition of
more than 25% of the common stock, par value, $.001, of Seller.
Act means the United States Federal Food,
Drug, and Cosmetic Act, as amended, and regulations promulgated
thereunder.
Action means any claim, action, suit,
arbitration, complaint, inquiry, audit, proceeding or
investigation, in each case by or before any Governmental
Authority.
Affiliate means, with respect to any Person,
any other Person directly or indirectly controlling or
controlled by, or under direct or indirect common control with,
such Person. For purposes of this definition, a Person shall be
deemed, in any event, to control another Person if it owns or
controls, directly or indirectly, more than fifty percent (50%)
of the voting equity of the other Person.
Agreement has the meaning set forth in the
Preamble of this Agreement.
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Allocation Schedule has the meaning set forth
in Section 2.7(a).
AMP has the meaning set forth in
Section 8.4(b)(i).
Applicable Permits means, to the extent
transferable under applicable Law, the permits, approvals,
licenses, franchises or authorizations, including the
Registrations, from any Governmental Authority held by Seller
that relate primarily or exclusively to the Product or the
Product Line Business set forth on
Schedule 1.1(a)(i) hereto.
Assets of any Person means all assets and
properties of any kind, nature, character and description
(whether real, personal or mixed, whether tangible or
intangible, whether absolute, accrued, contingent, fixed or
otherwise and wherever situated), including the goodwill related
thereto, operated, owned or leased by such Person, including
cash, cash equivalents, accounts and notes receivable, chattel
paper, documents, instruments, general intangibles, equipment,
inventory, goods and intellectual property.
Assigned Contracts means the Pre-Existing
Assigned Contracts and the Permitted Contract(s), and excluding
for all purposes, the Commercial Rebate Agreements.
Assignment of Product Intellectual Property
means the Assignment of Product Intellectual Property, in the
form which shall be mutually agreed by the Parties and then
attached hereto as Exhibit A.
Assumed Liabilities has the meaning set forth
in Section 2.3.
Basket Amount has the meaning set forth in
Section 10.4.
Best Price has the meaning set forth in
Section 8.4(b)(v).
Bill of Sale and Assignment and Assumption
Agreement means the Bill of Sale and Assignment and
Assumption Agreement, in the form which shall be mutually agreed
by the Parties and then attached hereto as Exhibit B.
Business Day means any day other than a
Saturday, a Sunday or a day on which banks in New York, New
York, United States of America are authorized or obligated by
Law to be closed.
Cardinal means Cardinal Health PTS, LLC.
Closing means the closing of the purchase and
sale of the Purchased Assets, and assignment and assumption of
the Assumed Liabilities contemplated by this Agreement.
Closing Date has the meaning set forth in
Section 3.1.
Code means the United States Internal Revenue
Code of 1986, as amended.
Commercial Rebate Agreements has the meaning
set forth in Section 8.4(c).
Confidentiality Agreement means (a) that
certain Confidentiality Agreement, dated as of December 28,
2005, between Seller and King, as amended by that certain letter
agreement, dated as of May 11, 2006, by and between Seller
and King, and (b) that certain Confidentiality Agreement,
dated as of August 15, 2006, between Seller and King.
Consents to the Assignments shall mean the
written consent of each of the third parties identified on
Schedule 2.5 to the assignment of the Contracts set
forth on such schedule, in each case in the applicable form(s)
which shall be mutually agreed by the Parties and then attached
hereto as Exhibit K.
Contracts means any and all binding written
commitments, contracts, purchase orders, leases, licenses,
easements, permits, instruments, commitments, arrangements,
undertakings, practices or other agreements.
Control or Controlled by
means, with respect to Intellectual Property, the ability of a
Party (collectively with its Affiliate(s)), whether by
ownership, license or otherwise, to grant a license or
sublicense.
Convertible Notes means all outstanding
6% Convertible Subordinated Notes due 2007, the outstanding
aggregate principal amount of which, as of June 30, 2006,
was $128,150,000.
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Distribution means activities related to the
distribution, marketing, promoting, offering for sale and
selling of the Product, including advertising, detailing,
educating, planning, promoting, conducting reporting, packaging,
storing, handling, shipping and communicating with Governmental
Authorities and third parties in connection therewith.
Effective Time has the meaning set forth in
Section 3.1.
Elan means Elan Corporation, plc.
Encumbrance means any lien (statutory or
otherwise), claim, charge, option, security interest, pledge,
mortgage, restriction, financing statement or similar
encumbrance of any kind or nature whatsoever (including any
conditional sale or other title retention agreement and any
lease having substantially the same effect as any of the
foregoing and any assignment or deposit arrangement in the
nature of a security device).
ERISA means the Employee Retirement Income
Security Act of 1974, as amended or any successor law, and
regulations and rules issued pursuant to that Act or any
successor law.
ERISA Affiliate of any entity means any other
entity (whether or not incorporated) that, together with such
entity, would be treated as a single employer under
Section 414 of the Code or Section 4001 of ERISA.
Escrow Account has the meaning set forth in
Section 2.9.
Escrow Agent means Wells Fargo Bank, National
Association, or such other party as may be mutually agreed by
the Parties.
Escrow Agreement means the escrow agreement
to be entered into at the Effective Time by and among Purchaser,
Seller and the Escrow Agent, substantially in the form attached
hereto as Exhibit J, pursuant to which the Escrow Amount
and the Retail Escrow Amount shall be held and disbursed.
Escrow Amount has the meaning set forth in
Section 2.9.
Excess Wholesale Inventory Value has the
meaning set forth in Schedule 2.8(b).
Exchange means the Nasdaq Global Market.
Exchange Act means the Securities Exchange
Act of 1934, as amended, and the rules and regulations
promulgated thereunder.
Excluded Assets means all of Sellers
Assets, whether or not relating to the Product or the Product
Line Business, other than the Purchased Assets.
Excluded Intellectual Property means all
rights, title and interest of Seller in and to Intellectual
Property, whether now existing or hereafter developed or
acquired (including the Seller Brands), other than the Product
Intellectual Property.
Excluded Liabilities has the meaning set
forth in Section 2.4.
Execution Date means the date set forth in
the Preamble of this Agreement.
FDA means the United States Food and Drug
Administration, or any successor agency thereto.
Final Allocation has the meaning set forth in
Section 2.7(b).
FSS has the meaning set forth in
Section 8.4(b)(iv).
GAAP means United States generally accepted
accounting principles.
Governmental Authority means any nation or
government, any provincial, state, regional, local or other
political subdivision thereof, any supranational organization of
sovereign states, and any entity, department, commission,
bureau, agency, authority, board, court, official or officer,
domestic or foreign, exercising executive, judicial, regulatory
or administrative functions of or pertaining to government.
Government Product Contracts means all
Contracts to which Seller is a party and pursuant to which
Seller sells the Product to a Governmental Authority either
singly or together with other pharmaceutical products of Seller.
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Government Rebates has the meaning set forth
in Section 8.4(b)(i).
Hired Employees has the meaning set forth in
Section 9.1(a).
HSR Act means the
U.S. Hart-Scott-Rodino
Antitrust Improvements Act of 1976, as amended, and the
rules and regulations promulgated thereunder.
ICS means Integrated Commercialization
Solutions, Inc.
ICS Agreement means the Commercial
Outsourcing Services Agreement entered into March 1, 2002
by and between ICS and Seller, as amended by: Amendment
No. 1 to Ligand Service Agreement dated September 4,
2003, Amendment No. 2 to Ligand Service Agreement dated
September 28, 2004, Amendment to Commercial Outsourcing
Services Agreement dated July 22, 2004, Fourth Amendment to
Commercial Outsourcing Services Agreement dated January 24,
2005, and Fifth Amendment to Commercial Outsourcing Services
Agreement dated April 29, 2005.
IND means Investigational New Drug
Application No. 61,328.
Intellectual Property means intellectual
property rights, including Trademarks, copyrights and Patents,
whether registered or unregistered, and all applications and
registrations therefor, domain names, web sites, know-how,
confidential information, trade secrets, and similar proprietary
rights in inventions, discoveries, analytic models,
improvements, products, systems, processes, techniques, devices,
methods, patterns, formulations and specifications.
Inventory means all inventories of the
finished Product (and all rights thereto) and active
pharmaceutical ingredient of the Product as described on
Schedule 1.1(c) hereto, which schedule shall
describe the Inventory quantities by SKU and shall be updated at
Closing.
IRS means the Internal Revenue Service of the
United States.
King Purchased Assets means, collectively,
all right, title and interest of Seller in and to the Assigned
Contracts, Inventory, Promotional Materials, Product Equipment,
Product Records, and all claims, counterclaims, credits, causes
of action, choses in action, rights of recovery and
rights of setoff relating to any of the foregoing.
King R&D Purchased Assets means,
collectively, all right, title and interest of Seller in and to
the Product and Product Line Business other than the King
Purchased Assets and the Excluded Assets, including without
limitation, the Registrations, Applicable Permits, all
regulatory files (including correspondence with regulatory
authorities) relating to the Applicable Permits (provided that
Seller may maintain a copy of such files for purposes of
fulfilling its ongoing obligations relating to the Product), any
intangible rights in and to the Product Records, the Product
Intellectual Property, and all claims, counterclaims, credits,
causes of action, choses in action, rights of recovery and
rights of setoff relating to any of the foregoing.
Knowledge means, with respect to Seller, the
actual knowledge of the Persons set forth on
Schedule 1.1(d) hereto.
Law means each provision of any currently
existing federal, provincial, state, local or foreign law,
statute, ordinance, order, code, rule or regulation, promulgated
or issued by any Governmental Authority, as well as any
judgments, decrees, injunctions or agreements issued or entered
into by any Governmental Authority specifically with respect to
Seller or the Product.
Liability means, collectively, any
indebtedness, guaranty, endorsement, claim, loss, damage,
deficiency, cost, expense, obligation or responsibility, fixed
or unfixed, known or unknown, choate or inchoate, liquidated or
unliquidated, secured or unsecured, direct or indirect, matured
or unmatured, or absolute, contingent or otherwise, including
any product liability.
LOI means, if executed by the Parties, a
letter of intent regarding the Transactions.
Losses means, with respect to any claim or
matter, all losses, expenses, obligations and other Liabilities
or other damages (whether absolute, accrued, contingent, fixed
or otherwise, or whether known or unknown, or due or to become
due or otherwise), diminution in value, monetary damages, fines,
fees, penalties, interest obligations,
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deficiencies, losses and expenses (including amounts paid in
settlement, interest, court costs, costs of investigators, fees
and expenses of attorneys, accountants, financial advisors and
other experts, and other expenses of litigation).
Mallinckrodt means Mallinckrodt, Inc.
Mallinckrodt Agreement means the letter
agreement between Mallinckrodt and Seller dated May 26,
2005.
Material Adverse Effect means any change or
effect that is materially adverse to the Product Line Business
taken as a whole, but shall exclude any change, effect or
circumstance resulting or arising from: (a) events,
circumstances, changes or effects that generally affect the
industries in which Seller operates, (b) general economic
or political conditions or events, circumstances, changes or
effects affecting the securities markets generally, and
(c) any circumstance, change or effect that results from
any action taken at the request of Purchaser (other than as
Seller is required to perform under this Agreement).
NDA(s) means the new drug application
covering the Product (NDA
No. 21-260),
including any supplements, amendments or modifications thereto,
or divisions thereof, including all correspondence under NDA
No. 21-260
between the FDA and Seller, in each case submitted to or
required by the FDA prior to the Effective Time.
NDC means the National Drug Code,
which is the eleven digit code registered by a company with the
FDA with respect to a pharmaceutical product.
Net Sales has the meaning set forth in
Schedule 2.6.
Non-FAMP has the meaning set forth in
38 U.S.C. § 8126 (h)(5).
Notice of Objection has the meaning set forth
in Section 2.8(d).
Organon means Organon Pharmaceuticals USA Inc.
Other Agreements means, collectively, the
Assignment of Product Intellectual Property, the Bill of Sale
and Assignment and Assumption Agreement, the Product License and
Supply Agreement Assignment, the Second Source Supply Agreement
Assignment, the Termination and Return of Rights Agreement
Assignment, the Technical Agreement
Avinza®
Assignment, the Quality Agreement for
Avinza®
Assignment, the Transition Services Agreement and the Escrow
Agreement.
Outside Date has the meaning set forth in
Section 11.1(a)(ii).
Party or Parties has the
meaning set forth in the Preamble of this Agreement.
Patents means United States and non-United
States patents, patent applications, patent disclosures,
invention disclosures and other rights relating to the
protection of inventions worldwide, and any and all right, title
and interest related to any of the foregoing, including without
limitation all reissues, reexaminations, divisions,
continuations,
continuations-in-part,
extensions or renewals of any of the foregoing as well as
supplementary protection certificates for medicinal products
provided under Council Regulation (EEC) No. 1768/92 of
June 18, 1992, and their equivalents.
PDE shall mean a primary detail equivalent
and be defined as equivalent to any of the following:
(a) one P1 Detail; (b) two P2 Details; or
(c) five P3 Details. Product Calls other than P1 Details,
P2 Details and P3 Details shall have no effect on any
calculation of PDEs. A P1 Detail is a Product
Call where the Product is presented in the first position. A
P2 Detail is a Product Call where the Product
is presented in the second position. A P3
Detail is a Product Call where the Product is
presented in the third position.
PDM Act means the Prescription Drug Marketing
Act of 1987, as amended.
Permitted Contract(s) means any Contracts,
including purchase orders, which relate to the Product or the
Product Line Business and which are entered into by Seller after
the Execution Date, which Contracts involve payment by Seller of
no more than $25,000 or extend for a term no longer than ninety
(90) days from the Closing Date, and which are not
otherwise material.
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Permitted Encumbrances means
(a) statutory liens for current Taxes of Seller not yet due
and payable or (b) mechanics, carriers,
workers, repairers and other similar liens arising
or incurred in the ordinary course of business relating to
obligations as to which there is no default on the part of
Seller.
Person means any individual, corporation,
partnership, joint venture, limited liability company, trust or
unincorporated organization or Governmental Authority.
Plan means any employment, bonus, deferred
compensation, incentive compensation, stock ownership, stock
purchase, stock appreciation, restricted stock, stock option,
phantom stock, performance, stock bonus, paid time
off, perquisite, fringe benefit, vacation, deferred
compensation, retiree medical or life insurance, supplemental
retirement, severance or other benefit plans, programs or
arrangements, and all employment, termination, severance,
retention or other contracts or agreements, or other program,
policy or arrangement.
Pre-Existing Assigned Contracts means those
Contracts, including purchase orders, related primarily or
exclusively to the Product and the Product Line Business which
are identified on Schedule 1.1(b) hereto; provided
that with respect to each of Sellers contracts with ICS or
Stericycle (formerly Universal Solutions International Inc.), in
the event Purchaser shall have entered into its own contracts
with such parties regarding Purchasers conduct of the
Product Line Business prior to Closing, then such Sellers
contracts with ICS or Stericycle (formerly Universal Solutions
International Inc.) shall not be included as PRE-EXISTING
ASSIGNED CONTRACTS AND SHALL NOT BE ASSIGNED TO OR ASSUMED BY
PURCHASER AS PART OF THE TRANSACTIONS.
Prescribers shall mean healthcare
institutions, hospitals, outpatient surgery centers and clinics,
as well as individual office-based primary care physicians
(i.e., internists, family practitioners and general
practitioners), other specialists, health care professionals or
para-professionals legally authorized to write prescriptions for
pharmaceutical products located in the Territory pursuant to
applicable Law.
Product means, the 30 mg, 60 mg,
90 mg and 120 mg finished dosage strengths of the
once-daily oral dosage microparticulate formulation developed by
Elan containing the active drug substance morphine and its salts
as its primary active ingredient currently marketed by Seller as
Avinza®,
and such other dosage strengths thereof, any reformulations or
derivations of the same (whether or not utilizing the Product
Patent Rights) and any other product sold or distributed under
the Product Marks.
Product Call shall mean an in person,
face-to-face
contact by a sales Representative with a Prescriber in the
Territory during which time the promotional message involving
the Product is presented in the first, second or third position.
Product Copyrights means any and all
copyrights owned, licensed, Controlled or otherwise utilized by
Seller primarily or exclusively related to the Product Line
Business, Product Trade Dress, Product Mark(s),
and/or
Promotional Materials.
Product Domain Names means the domain names
and web sites (including source code and layout) owned,
licensed, Controlled or otherwise utilized by Seller which
primarily or exclusively utilize the Product Mark(s) as
identified on Schedule 1.1(e) hereto.
Product Employee means those employees set
forth on Schedule 9.1(a)(1) hereto.
Product Equipment means the manufacturing
tools and test equipment owned by Seller and used primarily or
exclusively to manufacture the Product identified on
Schedule 1.1(f) hereto.
Product Intellectual Property means the
Product Patent Rights, Product Copyrights, Product Know-How,
Product Marks, and Product Trade Dress, in each case relating to
the Territory, and the Product Domain Names worldwide.
Product Inventory Data has the meaning set
forth in Section 6.1.
Product Know-How means as owned, licensed or
Controlled by Seller and primarily or exclusively related to the
Product Line Business or Product, the research and development
information, validation methods and procedures, unpatented
inventions, know-how, trade secrets, technical or other data or
information, or other materials, methods, systems, procedures,
processes, materials, developments or technology, including all
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biological, chemical, clinical, manufacturing and other
information or data, other than such know-how which is or
becomes the subject of a Patent.
Product License and Supply Agreement means
the Amended and Restated License and Supply Agreement, dated as
of November 12, 2002, by and between Seller, Elan and Elan
Management Limited, as amended and supplemented from time to
time prior to the Closing Date, which is attached hereto as
Exhibit L.
Product License and Supply Agreement
Assignment means the Assignment and Assumption of
Contract with respect to the Product License and Supply
Agreement, in the form which shall be mutually agreed by the
Parties and then attached hereto as Exhibit C.
Product Line Business has the meaning set
forth in the first Recital to this Agreement.
Product Mark(s) means the Trademark
Avinza®
and/or such
other Trademark(s) as registered with the PTO or other
equivalent Governmental Authority, which are owned, licensed,
Controlled or otherwise utilized by Seller
and/or its
Affiliates in the Territory to identify the Product in the
Territory which are identified on Schedule 1.1(g)
hereto, including without limitation, any and all right, title
and interest of Seller in and to such Trademarks outside the
Territory (if and to the extent Seller has any such rights,
title or interests).
Product Patent Rights means the Patents
licensed by Seller pursuant to the Product License and Supply
Agreement, which are identified on Schedule 1.1(k)
hereto.
Product Records means, in whatever medium
(e.g., audio, visual, print or electronic) relating to the
Product or the Product Line Business: (a) any and all data
and correspondence supporting
and/or
utilized or made in connection with obtaining
and/or
maintaining any of the Registrations
and/or the
drug master file for the Product, (b) raw
and/or
analysis data for pivotal trials and integrated summaries
(ISE/ISS) and all bio-analytical data in SAS transport, PC SAS
Version 6.06, or above, or other agreed format, (c) all
clinical data (phase I IV), (d) all data
from ongoing development of the compound utilized in the Product
(including marketing studies), (e) programs (analysis,
reports and supporting documentation) for trials for which data
is provided, (f) copies of SAS libraries (with
non-exclusive rights to use same) from Sellers analysis
programs relating to the Product, and (g) all books and
records owned by Seller relating to the Product (which shall be
copies to the extent not exclusive to the Product), including
copies of all customer and supplier lists, account lists, call
data, sales history, call notes, research data, marketing
studies, consultant reports, physician databases, and
correspondence (including invoices) with respect to the Product,
and all complaint files and adverse event reports and files, and
(h) copies of all data and information in the possession of
Seller relating to the activities of Organon
and/or IHS
or other entity providing support services to Seller which
relate to the Product, including for commercial rebates,
discounts, administrative fees, chargebacks
and/or
Government Rebates; provided, however, that (i) in
each case, Seller may exclude any Excluded Intellectual Property
contained therein, (ii) Seller may retain: (A) a copy
of any such books and records to the extent necessary for Tax,
accounting, litigation or other valid business purposes other
than the conduct of any business competitive with the Product or
the Product Line Business, (B) a copy of all such books and
records which relate to the Excluded Assets, and (C) all
books, documents, records and files (1) prepared in
connection with the Transactions, including bids received from
other parties and strategic, financial or Tax analyses relating
to the divestiture of the Purchased Assets, the Assumed
Liabilities, the Product and the Product Line Business, or
(2) maintained by Seller
and/or its
Representatives, agents or licensees in connection with their
respective Tax, legal, regulatory or reporting requirements
other than those relating to the Product or the Product Line
Business, (iii) any attorney work product, attorney-client
communications and other items protected by privilege shall be
excluded except to the extent relating to the Product or the
Product Line Business, and (iv) Seller shall be entitled to
redact from any such books and records any information that does
not relate to the Product or Product Line Business.
Product Trade Dress means the trade dress,
package designs, product inserts, labels, logos and associated
artwork owned by, licensed to or otherwise held by Seller and
used primarily or exclusively in connection with the Product,
Product Line Business or the packaging therefor, including
without limitation that which is identified on
Schedule 1.1(h) hereto, but specifically excluding
all Seller Brands used thereon other than the Product Marks.
Promotional Materials means the advertising,
promotional and media materials, sales training materials
(including any related outlines and quizzes/answers, if any),
trade show materials (including displays) and videos, including
materials containing post-marketing clinical data, if any, used
primarily or exclusively for the
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commercialization of the Product in the Territory by Seller
(including Distribution and sales promotion information, market
research studies and toll-free telephone numbers) identified on
Schedule 1.1(i) hereto.
Proxy Statement has the meaning set forth in
Section 6.6(a).
PTO means the United States Patent and
Trademark Office.
Purchase Price has the meaning set forth in
Section 2.6.
Purchase Price Bank Account means a bank
account in the United States to be designated by Seller in a
written notice to Purchaser at least three (3) Business
Days before the Closing.
Purchased Assets means, together, the King
Purchased Assets and the King R&D Purchased Assets.
Purchaser has the meaning set forth in the
Preamble of this Agreement.
Quality Agreement for
Avinza®
means the Quality Agreement for
Avinza®
dated April 10, 2006, by and between Seller and Cardinal,
as amended and supplemented from time to time prior to the
Closing Date, which is attached hereto as Exhibit P.
Quality Agreement for
Avinza®
Assignment means the Assignment and Assumption of
Contract with respect to the Quality Agreement for
Avinza®,
in the form which shall be mutually agreed by the Parties and
then attached hereto as Exhibit G.
Rebate Tail Period has the meaning set forth
in Section 8.4(b)(i).
Registrations means the regulatory approvals,
authorizations, licenses, applications, rights of reference,
permits, INDs, NDAs and other permissions held by Seller
relating primarily or exclusively to the Product in the
Territory
and/or
Product Line Business issued by Governmental Authorities in the
Territory to Seller as set forth on Schedule 1.1(j)
hereto.
Representatives means, with respect to any
Person, the directors, managers, employees, independent
contractors, agents or consultants of such Person.
Required Seller Stockholders means the
approval of the holders of a majority of the outstanding shares
of Sellers common stock.
Retail Escrow Account has the meaning set
forth in Section 2.8(c)(ii).
Retail Escrow Amount has the meaning set
forth in Section 2.8(c)(ii).
Retail Inventory Value Difference has the
meaning set forth in Schedule 2.8(b).
Retail Inventory Value Statement has the
meaning set forth in Section 2.8(d).
Retail Target has the meaning set forth in
Schedule 2.8(b).
Royalties has the meaning set forth in
Schedule 2.6.
Royalty Term means that period of time
(a) beginning on later of January 1, 2007 and the
Closing Date, and (b) ending on November 25, 2017.
SEC means the United States Securities and
Exchange Commission.
Second Source Supply Agreement means that
certain Manufacturing and Packaging Agreement, dated as of
February 13, 2004, between Seller and Cardinal, as amended
and supplemented from time to time prior to the Closing Date,
which is attached hereto as Exhibit M.
Second Source Supply Agreement Assignment
means the Assignment and Assumption of Contract with respect to
the Second Source Supply Agreement, in the form which shall be
mutually agreed by the Parties and then attached hereto as
Exhibit D.
Securities Act means the United States
Securities Act of 1933, as amended, and the rules and
regulations promulgated thereunder.
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Seller has the meaning set forth in the
Preamble of this Agreement.
Seller Brands means all Trademarks,
housemarks, tradenames, and trade dress owned, licensed,
Controlled or used by Seller, whether or not registered,
including the name Ligand, other than the Product
Marks.
Seller Disclosure Schedule means the
disclosure schedules delivered by Seller to Purchaser in
connection with this Agreement (it being expressly agreed that
disclosure of any item or matter under any Section or subsection
in such Seller Disclosure Schedule, or in attachments thereto,
and documents referred to therein, shall be deemed disclosure
for all purposes of Article IV).
Seller Plan means all Plans under which any
current or former Product Employee has accrued any benefit or
right whatsoever maintained by, contributed to or required to be
contributed to by Seller or any of its ERISA Affiliates or as to
which Seller or any of its ERISA Affiliates has any Liability.
Seller Recommendation means the
recommendation of the board of directors of Seller that the
board of directors of Seller has determined that the
Transactions are fair to and in the best interests of
Sellers stockholders.
Seller Stockholders Meeting has the
meaning set forth in Section 6.6(c).
Sellers SEC Filings means all forms,
reports and other documents required to be filed by Seller under
the Securities Act or Exchange Act, as the case may be since and
including January 1, 2004.
SKU means stock keeping unit.
Subsidiary means, with respect to any Person,
any and all corporations, partnerships, limited liability
companies, joint ventures, associations and other entities
controlled by such Person.
Superior Proposal means an Acquisition
Proposal, which (a) in the good faith judgment of the board
of directors of Seller (after considering the advice of its
financial advisors and outside legal counsel) would if
consummated result in a transaction that (i) if for the
Product, is more favorable to Seller than the Transactions, or
(ii) if for equity interests in Seller or substantially all
of the Assets of Seller, including the Product, is more
favorable, taken as a whole, to Sellers stockholders than
the Transactions, and the board of directors of Seller intends
to terminate this Agreement in connection with such
determination, or (b) does not require termination of this
Agreement or any of the Other Agreements as a condition to
consummation of such Acquisition Proposal.
Tax or Taxes means any and
all taxes, assessments, levies, tariffs, duties or other charges
or impositions in the nature of a tax (together with any and all
interest, penalties, additions to tax and additional amounts
imposed with respect thereto) imposed by any Governmental
Authority, including income, estimated income, gross receipts,
profits, business, license, occupation, franchise, capital
stock, real or personal property, sales, use, transfer, value
added, employment or unemployment, social security, disability,
alternative or add-on minimum, customs, excise, stamp,
environmental, commercial rent or withholding taxes, and shall
include any Liability for Taxes of any other Person under
applicable Law, as a transferee or successor, by contract or
otherwise.
Tax Return means any report, return
(including any information return), claim for refund, election,
estimated Tax filing or payment, request for extension,
document, declaration or other information or filing required to
be supplied to any Governmental Authority with respect to Taxes,
including attachments thereto and amendments thereof.
Technical Agreement
Avinza®
means the Technical Agreement
Avinza®
dated June 10, 2003, by and between Seller and Elan
Holdings, Incorporated, as amended and supplemented from time to
time prior to the Closing Date, which is attached hereto as
Exhibit O.
Technical Agreement
Avinza®
Assignment means the Assignment and Assumption of
Contract with respect to the Technical Agreement
Avinza®,
in the form which shall be mutually agreed by the Parties and
then attached hereto as Exhibit F.
Termination and Return of Rights Agreement
means the Termination and Return of Rights Agreement, dated as
of January 1, 2006, by and between Seller and Organon USA
Inc., as amended and supplemented from time to time prior to the
Closing Date, which is attached hereto as Exhibit N.
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Termination and Return of Rights Agreement
Assignment means the Assignment and Assumption of
Contract with respect to the Termination and Return of Rights
Agreement, in the form which shall be mutually agreed by the
Parties and then attached hereto as Exhibit E.
Termination Fee has the meaning set forth in
Section 11.2(b).
Territory means the United States of America
and its territories and Canada.
Trademark means trademarks, service marks,
certification marks, trade dress, Internet domain names, trade
names, identifying symbols, designs, product names, company
names, slogans, logos or insignia, whether registered or
unregistered, and all common law rights, applications and
registrations therefor, and all goodwill associated therewith.
Transactions means the transactions
contemplated by this Agreement.
Transfer Taxes means any and all transfer,
documentary, sales, use, gross receipts, stamp, registration,
value added, recording, escrow and other similar Taxes and fees
(including any penalties and interest) incurred in connection
with the Transactions (including recording and escrow fees and
any real property or leasehold interest transfer or gains tax
and any similar Tax).
Transition Services Agreement means that
certain Transition Services Agreement, dated as of the date
hereof, between Seller and Purchaser, in the form which shall be
mutually agreed by the Parties and then attached hereto as
Exhibit H.
Wholesale Target has the meaning set forth in
and calculated pursuant to Schedule 2.8(b)(i).
1.2 Other Definitional Provisions.
(a) When a reference is made in this Agreement to an
Article, Section, Exhibit or Schedule, such reference is to an
Article or Section of, or an Exhibit or Schedule to, this
Agreement unless otherwise indicated.
(b) The words hereof, herein,
hereto and hereunder and words of
similar import, when used in this Agreement, shall refer to this
Agreement as a whole and not to any particular provision of this
Agreement.
(c) The terms defined in the singular has a comparable
meaning when used in the plural, and vice versa.
(d) Words of one gender include the other gender.
(e) References to a Person are also to its successors and
permitted assigns.
(f) The term dollars and $ means
United States dollars.
(g) The word including means including
without limitation and the words include and
includes have corresponding meanings.
ARTICLE II
Purchase and
Sale
2.1 Transfer of Purchased
Assets. At the Effective Time, on the terms and
subject to the conditions hereof and in consideration of the
Purchase Price, Seller will sell, convey, transfer, assign and
deliver to King, and King will purchase, take delivery of and
acquire from Seller, all of Sellers right, title and
interest in and to the King Purchased Assets, and Seller will
sell, convey, transfer, assign and deliver to King R&D, and
King R&D will purchase, take delivery of and acquire from
Seller, all of Sellers right, title and interest in and to
the King R&D Purchased Assets.
2.2 Excluded Assets. The Parties
acknowledge and agree that Seller is not selling, conveying,
transferring, delivering or assigning any rights whatsoever to
the Excluded Assets to Purchaser, and Purchaser is not
purchasing,
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taking delivery of or acquiring any rights whatsoever to the
Excluded Assets from Seller. Without limiting the foregoing:
(a) Purchaser expressly acknowledges it is not acquiring
any rights whatsoever to the Excluded Intellectual Property,
including the Seller Brands thereof and any other logos or
Trademarks of Seller not included in the Product Intellectual
Property, and
(b) Purchaser expressly acknowledges it is not acquiring
any rights whatsoever to any accounts receivable (including any
payments received with respect thereto on or after the Closing,
unpaid interest accrued on any such accounts receivable and any
security or collateral related thereto) arising from sales of
the Product on or prior to the Closing Date (collectively, the
Accounts Receivable).
2.3 Assumed Liabilities. As of the
Effective Time, Purchaser shall assume and pay, perform or
otherwise discharge, in accordance with their respective terms
and subject to the respective conditions thereof, only the
following Liabilities (collectively, the Assumed
Liabilities):
(a) any Liability arising after the Effective Time under
any Assigned Contract; provided that, for the avoidance
of doubt, to the extent Seller has not made all or any portion
of the Forty Seven Million Seven Hundred Fifty Thousand Dollar
($47,750,000) early termination payment to be made pursuant to
Section 3(c) of the Termination and Return of Rights
Agreement prior to the Effective Time, any and all such unpaid
amounts (excluding any penalty amounts, interest or other
amounts due thereon for Sellers failure to pay such
amounts prior to the Effective Time) shall constitute an Assumed
Liability;
(b) any Liability in respect of Hired Employees arising
after Purchasers employment of Hired Employees, except to
the extent that the same constitute Excluded Liabilities or as
otherwise provided in Article IX to be retained by
Seller; and
(c) any other Liability, if any, specifically and to the
extent set forth on Schedule 2.3 hereto.
For avoidance of doubt, nothing in this Section 2.3
is intended to, or shall be interpreted to, limit or otherwise
reduce the Liabilities of Purchaser as they may occur
and/or exist
after the Effective Time solely by virtue of Purchasers
ownership of the Purchased Assets or operation of the Product
Line Business, but rather, this Section 2.3 is
solely intended to identify and provide for the assumption by
Purchaser of those Liabilities of Seller that are specifically
assumed by Purchaser hereunder and which, but for such
assumption, would remain Liabilities of Seller.
2.4 Excluded Liabilities. Seller
shall retain and shall be responsible for paying, performing and
discharging when due, and Purchaser shall not assume or have any
responsibility for (i) any Liability of Seller for Taxes
(except as otherwise provided in Section 8.8(a) with
respect to Transfer Taxes), (ii) any penalties or interest
resulting from failure to timely pay amounts due under any
Assigned Contracts to the extent relating to any time prior to
the Effective Time, and (iii) any and all Liabilities other
than the Assumed Liabilities (the Excluded
Liabilities).
2.5 Seller to Obtain Consent of Third
Parties. On the Closing Date, Seller shall assign
to Purchaser, and Purchaser will assume, the Assigned Contracts
(to the extent provided in this Agreement), in each case to the
extent permitted by, and in accordance with, applicable Law.
Seller shall, at its sole cost and expense, use commercially
reasonable efforts to obtain the consent of any third party (in
the form which shall be mutually agreed by the Parties and then
attached hereto as Exhibit K) required under
any Assigned Contract to the assignment by Seller to Purchaser
of the applicable Assigned Contract. Notwithstanding anything
herein to the contrary, if the assignment or assumption of all
or any portion of any rights or obligations under any Assigned
Contract shall require the consent of any other party thereto or
any other third party that has not been obtained prior to the
Effective Time, this Agreement shall not constitute an agreement
to assign, license, sublicense, lease, sublease, convey or
otherwise transfer any rights or obligations under any such
Assigned Contract. In order, however, to provide Purchaser the
full realization and value of every Assigned Contract of the
character described in the immediately preceding sentence as
soon as practicable after the Effective Time, Seller shall, at
its sole cost and expense, after the Closing, use commercially
reasonable efforts to obtain those consents from any Persons (in
the form which shall be mutually agreed by the Parties and then
attached hereto as Exhibit K) not obtained
prior to the Effective Time necessary to
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effectuate the assignment of any Assigned Contracts. Purchaser
shall reasonably cooperate with Seller at Purchasers sole
cost and expense in connection with such undertaking of Seller
and Seller shall keep Purchaser fully informed in a timely
manner as to all developments regarding the same, including
promptly providing Purchaser with copies of all material
correspondence, drafts and other material communications
regarding same.
Notwithstanding the foregoing prior to Closing Purchaser shall
use its best efforts to enter into its own contracts with ICS
and Stericycle (formerly Universal Solutions International Inc.)
regarding Purchasers conduct of the Product Line Business
following Closing.
2.6 Purchase Price. In addition to
any other amounts due hereunder (including, without limitation,
the Royalties to be paid in accordance with
Schedule 2.6), in consideration of the sale,
assignment, conveyance, license and delivery of the Purchased
Assets under Article II, Purchaser shall, upon the
Closing, assume the Assumed Liabilities and subject to the terms
and conditions hereof pay to Seller, by wire transfer of
immediately available funds directly to an account designated by
Seller, the aggregate of the following amounts, subject to the
adjustments set forth in Section 2.8 (as adjusted,
the Purchase Price):
(a) Two Hundred Sixty-Five Million Dollars ($265,000,000);
plus
(b) to the extent paid to Organon by Seller prior to
Closing, reimbursement for up to Forty Seven Million Seven
Hundred Fifty Thousand Dollars ($47,750,000) in early
termination payments made pursuant to Section 3(c) of the
Termination and Return of Rights Agreement.
Payment of the Purchase Price at Closing shall be subject to
reduction for any amounts required to be withheld in escrow
pursuant to Section 2.8, Section 2.9 and
any other credits due to Purchaser under the terms of this
Agreement.
2.7 Purchase Price Allocation.
(a) Subject to the adjustments described in
Section 2.8, any payments or other amounts that are
required to be treated as part of the Purchase Price for federal
income tax purposes shall be allocated among the Purchased
Assets as set forth on Schedule 2.7 (the
Allocation Schedule).
(b) Within fifteen (15) days after the final
determination of the Retail Inventory Value Statement pursuant
to Section 2.8, Purchaser shall prepare and deliver
to Seller, an amended Allocation Schedule (the Final
Allocation) that reflects the Retail Inventory Value
Statement and any resulting adjustments in the allocation of the
payments or other amounts treated under the Allocation Schedule
pursuant to Section 2.7(a).
(c) The Allocation Schedule and Final Allocation shall each
be prepared based on independent third party valuation and in
accordance with GAAP. In accordance with Section 1060 of
the Code and the Treasury Regulations thereunder, Purchaser and
Seller agree, unless otherwise required pursuant to a
determination within the meaning of
Section 1313(a) of the Code, to be bound by the Final
Allocation, to file all Tax Returns (including IRS Form 8594 and
any supplemental or amended IRS Form 8594, each of which
IRS Form 8594 shall be prepared by Purchaser and provided to
Seller) in accordance with the Final Allocation, and not to take
any position inconsistent with the Final Allocation in the
course of any audit, examination, other administrative or
judicial proceeding.
2.8 Inventory Value Adjustments.
(a) On the Closing Date, Seller shall provide Purchaser
with a report based on Product Inventory Data provided by Seller
in accordance with this Agreement setting forth (i) the
calculated amounts for each of the items enumerated on
Schedule 2.8(b) together with all supporting data
used to calculate same, (ii) whether, and the extent to
which, the Wholesale Target and the Retail Target have been met,
and (iii) Sellers
out-of-pocket
cost (without markup) paid as purchase price to Elan
and/or
Cardinal between the Execution Date and the Effective Time for
finished Product. The foregoing report shall be accompanied by a
written certification of the CFO of Seller as to the good faith
completeness and accuracy of such report.
(b) If, at Closing, the Wholesale Target (as adjusted to
allow Seller a credit against the Wholesale Target for
Sellers
out-of-pocket
cost (without markup) paid as purchase price to Elan
and/or
Cardinal between the Execution Date and the Effective Time for
the finished Product) has not been achieved, the Purchase Price
shall be adjusted downward by the Excess Wholesale Inventory
Value.
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(c) If, at Closing, the Retail Target has not been
achieved, then for each One Dollar ($1.00) of Retail Inventory
Value Difference up to and including Ten Million Dollars
($10,000,000), the Purchase Price shall be adjusted downward by
One Dollar ($1.00), and in addition:
(i) if Retail Inventory Value Difference is greater than
Ten Million Dollars ($10,000,000), then for each One Dollar
($1.00) of Retail Inventory Value Difference in excess of Ten
Million Dollars ($10,000,000), the Purchase Price shall be
adjusted downward by Fifty Cents ($0.50); or
(ii) if Retail Inventory Value Difference is less than Ten
Million Dollars ($10,000,000), then the difference between
Retail Inventory Value Difference and Ten Million Dollars
($10,000,000) (the Retail Escrow Amount)
shall be withheld from Purchase Price paid at Closing and
delivered to the Escrow Agent for deposit into a separate escrow
account (the Retail Escrow Account), and held
pursuant to the provisions of the Escrow Agreement.
(d) As promptly as practicable, but in any event not later
than thirty (30) days after the Closing Date, Purchaser
shall prepare and deliver to Seller a statement calculating the
Retail Inventory Value Difference (the Retail Inventory
Value Statement). During the thirty (30) day
period immediately following Sellers receipt of the Retail
Inventory Value Statement, Seller and Purchaser shall each
review the Product Inventory Data to evaluate the Retail
Inventory Value Statement. The Retail Inventory Value Statement
shall become final and binding upon Purchaser and Seller at the
end of such thirty (30) day period, unless Seller objects
to the Retail Inventory Value Statement, in which case it shall
send written notice (the Notice of Objection)
to Purchaser within such period, setting forth in specific
detail the basis for its objection and Sellers proposal
for any adjustments to the Retail Inventory Value Statement. If
a timely Notice of Objection is received by Purchaser, then the
Retail Inventory Value Statement shall become final and binding
(except as provided below with respect to resolution of
disputes) on Seller and Purchaser on the first to occur of
(i) the date Seller and Purchaser resolve in writing any
differences they have with respect to the matters specified in
the Notice of Objection, or (ii) the date all matters in
dispute are finally resolved in writing by the Accountants, in
each case as provided below. Seller and Purchaser shall seek in
good faith to reach agreement with respect to any such proposed
adjustment or that no such adjustment is necessary within twenty
(20) days following Purchasers receipt of the Notice
of Objection. If agreement is reached in writing within such
twenty (20) day period as to all proposed adjustments, or
that no adjustments are necessary, Purchaser shall revise the
Retail Inventory Value Statement accordingly. If Seller and
Purchaser are unable to reach agreement within twenty
(20) days following receipt of the Notice of Objection,
then the Accountants shall be engaged at that time to review the
Retail Inventory Value Statement, and shall make a determination
as to the resolution of any adjustments. The determination of
the Accountants shall be delivered as soon as practicable
following engagement of the Accountants, but in no event more
than sixty (60) days thereafter, and shall be final,
conclusive and binding upon Seller and Purchaser and Purchaser
shall revise the Retail Inventory Value Statement accordingly.
The Parties agree that judgment may be entered on such
determination in any court having jurisdiction. Seller, on the
one hand, and Purchaser, on the other hand, shall each pay
one-half of the cost of the Accountants.
(e) Within three (3) Business Days after the date on
which the Retail Inventory Value Statement becomes final and
binding on Seller and Purchaser pursuant to
Section 2.8(d), then:
(i) To the extent the Retail Inventory Value Statement (as
final and binding on the Parties in accordance with
Section 2.8(d)) provides that Seller owes a payment
to Purchaser, Seller shall pay Purchaser an amount equal to the
amount due as follows:
(A) first, amounts contained in the Retail Escrow Account
up to and including the amount due shall be paid to Purchaser
pursuant to the terms of the Retail Escrow Agreement; and
(B) second, to the extent such amounts held in the Retail
Escrow Account are insufficient to satisfy in full such amounts
due, Seller shall pay to Purchaser an amount equal to the
remaining amounts due which have not been paid to Purchaser from
the Retail Escrow Account; or
(ii) To the extent the Retail Inventory Value Statement (as
final and binding on the Parties in accordance with
Section 2.8(d)) provides that Purchaser owes a
payment to Seller, Purchaser shall pay Seller such amount due
(exclusive of the return of funds in the Retail Escrow Account
pursuant to Section 2.8(e)(iii)); and
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(iii) All amounts remaining in the Retail Escrow Account
(after giving effect to Section 2.8(e)(i), if
applicable), if any, shall be paid to Seller pursuant to the
terms of the Retail Escrow Agreement.
2.9 Escrow. At the Closing,
Purchaser shall, in addition to any other reductions to the
Purchase Price paid at Closing to be made pursuant to this
Article II, if any, withhold Fifteen Million Dollars
($15,000,000) (the Escrow Amount) from the
Purchase Price paid at Closing, which Escrow Amount shall be
delivered to the Escrow Agent for deposit into a separate escrow
account (the Escrow Account). The Escrow
Amount shall be held pursuant to the provisions of Escrow
Agreement. The Escrow Amount will be available to compensate
Purchaser for Losses as provided in Article X,
subject to the terms, conditions and limitations in the Escrow
Agreement. On the six (6)-month anniversary of the Closing Date,
Seven Million Five-Hundred Thousand Dollars ($7,500,000) (or
such lesser amount then remaining in the Escrow Account) shall
be released from the Escrow Account to Seller, provided
that, if any good faith claims for indemnification by Purchaser
have been made pursuant to this Agreement and remain unresolved
at such time and an amount equal to such unresolved good faith
claims would not remain in the Escrow Account following such
release from the Escrow Account, an amount equal to such good
faith claims shall remain in the Escrow Account and all other
amounts in the Escrow Account at such time, up to a maximum of
Seven Million Five-Hundred Thousand Dollars ($7,500,000), shall
be released from the Escrow Account to Seller. On the one
(1)-year anniversary of the Closing Date, all amounts then
remaining in the Escrow Account shall be released from the
Escrow Account to Seller, provided that, if any good
faith claims for indemnification by Purchaser have been made
pursuant to this Agreement and remain unresolved at such time,
an amount equal to such good faith claims shall remain in the
Escrow Account and all other amounts in the Escrow Account at
such time shall be released from the Escrow Account to Seller.
If any amounts remain in the Escrow Account after the one
(1)-year anniversary of the Closing Date in order to satisfy
unresolved good faith claims for indemnification made by
Purchaser pursuant to this Agreement, any and all such amounts
remaining in the Escrow Account following the resolution of such
claims, if any, shall be promptly released to Seller.
2.10 Risk of Loss. Until the
delivery to Purchaser pursuant to this Agreement, following the
Effective Time, any loss of or damage to the Purchased Assets
from fire, flood, casualty or any other similar occurrence shall
be the sole responsibility of Seller. As of the Effective Time,
title to the Purchased Assets shall be transferred to Purchaser.
After the delivery to Purchaser pursuant to
Section 3.2(a)(i) following the Effective Time,
Purchaser shall bear all risk of loss associated with the
Purchased Assets and shall be solely responsible for procuring
adequate insurance to protect the Purchased Assets against any
such loss.
ARTICLE III
Closing
3.1 Closing. Upon the terms and
subject to the conditions of this Agreement, the Closing shall
be held on a date following the satisfaction or waiver of all of
the conditions set forth in Article VII, which shall
be specified by Purchaser and be, if such conditions have been
satisfied by such time, no later than December 31, 2006,
such date (the Closing Date) and take place
through facsimile exchange of signature pages together with
email exchange of electronic files in
Adobe®
PDF file format containing copies of the executed documents,
unless the Parties otherwise agree. The Parties will exchange
(or cause to be exchanged) at the Closing the funds, agreements,
instruments, certificates and other documents, and do, or cause
to be done, all of the things respectively required of each
Party as specified in Section 3.2. The Closing shall
be deemed to have occurred at 11:59 p.m. eastern time on
such day on which the Closing occurs (the Effective
Time).
3.2 Transactions at Closing. At the
Closing, subject to the terms and conditions hereof:
(a) Sellers Actions and
Deliveries. Seller shall deliver or cause to be
delivered to Purchaser:
(i) the Inventory (which shall be delivered at the
facilities of ICS, Mallinckrodt, Elan,
and/or
Cardinal, as the case may be);
(ii) the forms of all of the Other Agreements have been
mutually agreed by the Parties and attached to this Agreement as
the appropriate Exhibits;
(iii) executed counterparts of each of the Other Agreements
to which it is a party;
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(iv) a letter from Seller to the FDA, duly executed by
Seller, transferring the rights to the Registrations to
Purchaser, in form and substance reasonably satisfactory to
Purchaser, set forth on Schedule 3.2(a)(iv) hereto;
(v) a certificate of a duly authorized officer of Seller
certifying as to the matters set forth in
Sections 7.2(a) and (b);
(vi) such other documents and instruments as may be
reasonably necessary to effect or evidence the Transactions,
including, without limitation reasonably stored and organized
Product Records;
(vii) executed Consents to the Assignments in the forms
that have been mutually agreed by the Parties with respect to
each party set forth on Schedule 2.5 hereto.
(b) Purchasers Actions and
Deliveries. Purchaser shall deliver or cause to
be delivered to Seller:
(i) the Purchase Price (subject to adjustments and
reductions as set forth in Section 2.6), by wire
transfer of immediately available funds directly to the Purchase
Price Bank Account designated by Seller;
(ii) the forms of all of the Other Agreements have been
mutually agreed by the Parties and attached to this Agreement as
the appropriate Exhibits;
(iii) executed counterparts of each of the Other Agreements
to which it is a party;
(iv) a letter from Purchaser to the FDA duly executed by
Purchaser, assuming responsibility for Registrations from
Seller, in form and substance reasonably satisfactory to Seller,
as set forth on Schedule 3.2(b)(iv);
(v) a certificate of a duly authorized officer of Purchaser
certifying as to the matters set forth in
Sections 7.3(a) and (b); and
(vi) such other documents and instruments as may be
reasonably necessary to effect or evidence the Transactions.
ARTICLE IV
Representations
and Warranties of Seller
Seller hereby represents and warrants to Purchaser, as of the
Execution Date, as follows:
4.1 Organization. Seller is a
corporation duly organized, validly existing and in good
standing under the laws of Delaware. Seller has all requisite
corporate power and authority to own, lease and operate, as
applicable, the Purchased Assets and to carry on the Product
Line Business as presently conducted.
4.2 Due Authorization. Seller has
all requisite corporate power and authority to execute, deliver
and perform its obligations under this Agreement and the Other
Agreements, and the execution and delivery of this Agreement and
the Other Agreements and the performance of all of its
obligations hereunder and thereunder have been duly authorized
by Seller. The execution and delivery of this Agreement and the
performance by Seller of its obligations hereunder have been
authorized by all requisite board and, only as of the Closing
Date, all requisite stockholder action.
4.3 No Conflicts;
Enforceability. The execution, delivery and
performance of this Agreement and the Other Agreements by Seller
(a) are not prohibited or limited by, and will not result
in the breach of or a default under, any provision of the
certificate of incorporation or bylaws of Seller or any
Subsidiary of Seller, (b) assuming all of the consents,
approvals, authorizations and permits described in
Section 4.7 have been obtained and all the filings
and notifications described in Section 4.7 have been
made and any waiting periods thereunder have terminated or
expired, except as would not reasonably be expected to have a
Material Adverse Effect, do not conflict with or result in
violation or breach of any Law applicable to Seller, and
(c) except as set forth on Schedule 4.3 of the
Seller Disclosure Schedule, does not conflict with, result in a
material breach of, constitute (with or without due notice or
lapse of time or both) a material default under, result in the
acceleration of obligations under, create in any party the right
to terminate, modify or cancel, or require any notice, consent
or waiver under, any agreement,
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including without limitation any Assigned Contracts, or
instrument binding on Seller prior to the Effective Time or any
applicable order, writ, injunction or decree of any court or
Governmental Authority to which Seller is a party or by which
Seller is bound or to which any of its Assets is subject. This
Agreement and the Other Agreements have been duly executed and
delivered by Seller, and constitute the legal, valid and binding
obligations of Seller, enforceable against Seller in accordance
with their respective terms, except as enforceability may be
limited or affected by applicable bankruptcy, insolvency,
moratorium, reorganization or other Laws of general application
relating to or affecting creditors rights generally.
4.4 Title; Assets. Except as set
forth on Schedule 4.4 of the Seller Disclosure
Schedule, Seller has good and valid title to the Purchased
Assets, whether by ownership, leases, licenses or other
instruments granting Seller the right to use the Purchased
Assets, in each case free and clear of all Encumbrances other
than the Permitted Encumbrances. Neither Seller nor any
Affiliate of Seller has any right, title or interest in or to
any product containing morphine or other opioid as an active
pharmaceutical ingredient in any stage of development. Seller
does not lease any manufacturing tools or test equipment
utilized in the conduct of the Product Line Business. The
Purchased Assets transferred to Purchaser pursuant to this
Agreement constitute all assets necessary and sufficient for the
conduct of the Product Line Business as has been conducted by
Seller and as is presently conducted by Seller, other than
permits issued by the U.S. Drug Enforcement Agency and
controlled substances permits issued by State Governmental
Authorities.
4.5 Intellectual Property.
(a) Schedule 4.5(a) of the Seller Disclosure
Schedule sets forth any and all Patents licensed, owned or
Controlled by Seller (i) pursuant to the Product License
and Supply Agreement,
and/or
(ii) relating to the Product or its use or manufacture.
(b) Included in the Product Intellectual Property are all
rights in and to any and all Intellectual Property necessary and
sufficient for the conduct of the Product Line Business as has
been conducted by Seller and as is presently conducted by
Seller, and all such rights are included in the Purchased Assets
transferred to Purchaser pursuant to this Agreement.
(c) Except as set forth on Schedule 4.5(c) of
the Seller Disclosure Schedule or as would not, individually or
in the aggregate, reasonably be expected to have a Material
Adverse Effect, all Intellectual Property necessary for the
conduct of the Product Line Business is under the Control of
Seller.
(d) Except as set forth on Schedule 4.5(d) of
the Seller Disclosure Schedule, (i) to Sellers
Knowledge the Product Intellectual Property is enforceable and
valid and (ii) none of the Product Intellectual Property
has been or is the subject of: (A) any pending adverse
judgment, injunction, order, decree or agreement restricting
(x) its use in connection with the Product or the Product
Line Business or (y) assignment or license thereof by
Seller; or (B) any threatened litigation or claim of
infringement threatened or made, in each case made in writing or
to Sellers Knowledge made otherwise; or (C) any
pending litigation; or (D) any requests for royalty
payments or offers for licenses to Intellectual Property which
would relate to the Product or the Product Line Business, in
each case made in writing or to Sellers Knowledge made
otherwise; or (E) to Sellers Knowledge any
discussions relating to any of the matters addressed by
Sections 4.5(d)(ii)(B) or (D).
(e) Except as set forth on Schedule 4.5(e) of
the Seller Disclosure Schedule, all Product Intellectual
Property is under the Control of Seller.
(f) Except as set forth on Schedule 4.5(f) of
the Seller Disclosure Schedule, (i) neither Seller nor any
of its Affiliates has granted any licenses to the Product
Intellectual Property to third parties; (ii) neither Seller
nor any of its Affiliates, nor to Sellers Knowledge, any
other Person, is party to any agreements with third parties that
materially limit or restrict use of the Product Intellectual
Property or require any payments for their use; and
(iii) to Sellers Knowledge, no other Person has any
joint ownership or royalty interest in the Product Intellectual
Property.
(g) Except as set forth on Schedule 4.5(g) of
the Seller Disclosure Schedule, (i) to Sellers
Knowledge, the use or sale of the Product in the Territory, and
the manufacture of the Product in the Territory or where
manufactured by or behalf of Seller for use or sale in the
Territory, does not and will not infringe any valid intellectual
property right
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of any third party, and (ii) neither Seller nor any of its
Affiliates has received written notice of a claim of any such
infringement.
(h) Seller has not received written notice of any
misappropriation or infringement of, any of the Product
Intellectual Property by any Person.
(i) All issuance, renewal, maintenance and other payments
that are or have become due with respect to the Product
Intellectual Property have been timely paid by or on behalf of
Seller, except as would not reasonably be expected to have a
Material Adverse Effect.
(j) To Sellers Knowledge, there are no actual or
threatened inventorship challenges, interferences declared or
assertions of invalidity with respect to any Patents included in
the Product Intellectual Property.
(k) (i) to Sellers Knowledge, the use of the
Product Mark(s) in the Territory does not infringe any
intellectual property right, including Trademark, of any third
party, and (ii) neither Seller nor any of its Affiliates
has received written notice of any such infringement claims.
(l) Seller and its Affiliates have taken reasonable
measures to maintain in confidence all Product Know-How, except
as would not reasonably be expected to have a Material Adverse
Effect.
(m) To Sellers Knowledge, except as set forth on
Schedule 4.5(m) of the Seller Disclosure Schedule,
no present or former employee or consultant of Seller and no
other Person owns or has any proprietary, financial or other
interest, direct or indirect, in the Product Intellectual
Property.
4.6 Litigation. Except as set forth
on Schedule 4.6 of the Seller Disclosure Schedule
and as would not reasonably be expected to have a Material
Adverse Effect or would prevent the consummation by Seller of
the Transactions, as of the Execution Date, to Sellers
Knowledge, there is no Action pending or threatened related to
the Product, the Product Line Business or the Transactions.
4.7 Consents. Except for the
Consents to Assignments required to be delivered by Seller to
Purchaser pursuant to Section 7.2(c), the approval
of the Required Seller Stockholders, any requisite filings under
the HSR Act and the expiration or termination of the waiting
period under the HSR Act, any other necessary premerger or
competition filings, and all of the filings and other actions
contemplated set forth on Schedule 4.7 of the Seller
Disclosure Schedule (including the letters to the FDA
contemplated by Sections 3.2(a)(iv) and
3.2(b)(iv), any applicable filings required under the
Exchange Act, any applicable Blue Sky Laws and the rules and
regulations of the Exchange, and as may be necessary as a result
of any facts or circumstances relating solely to Purchaser), no
notice to, filing with, authorization of, exemption by, or
consent of, any Person, including any Governmental Authority, is
required for Seller to consummate the Transactions, except where
the failure to make such filings or notifications, or obtain
such consents, approvals, authorizations or permits, would not,
individually or in the aggregate, reasonably be expected to have
a Material Adverse Effect
4.8 Taxes.
(a) There are no liens for Taxes (other than liens for
current Taxes not yet due and payable) on the Purchased Assets
or the Inventory.
(b) Except as set forth on Schedule 4.8, there
are no ongoing or pending or, to Sellers Knowledge,
threatened Actions or audits concerning any Tax Liability of
Seller attributable to or associated with any of the Purchased
Assets or the Product Line Business.
4.9 Employee Matters.
(a) Plans and Material
Documents. Schedule 4.9 of the Seller
Disclosure Schedule lists all material Seller Plans. Seller has
made available to Purchaser a true and complete copy of each
Seller Plan.
(b) Compliance. Each Seller Plan has been
operated in all material respects in accordance with its terms
and the requirements of all applicable Laws. Seller has
performed all material obligations required to be performed by
it under, is not in any material respect in default under or in
material violation of, and Seller has no Knowledge of any
material default or violation by any party to, any Seller Plan.
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(c) Qualification of Certain Plans. Each
Plan that is intended to be qualified under Section 401(a)
of the Code or Section 401(k) of the Code has timely
received a favorable determination or opinion letter from the
IRS covering all of the provisions applicable to the Seller Plan
for which determination or opinion letters are currently
available that the Seller Plan is so qualified and no fact or
event has occurred since the date of such determination or
opinion letter or letters from the IRS to adversely affect the
qualified status of any such Seller Plan or the exempt status of
any such trust.
(d) Collective Bargaining
Agreements. With respect to Product Employees,
(i) Seller is not a party to, or bound by, the terms of any
collective bargaining agreement, and is under no obligation to
collectively bargain with any labor organization as those terms
are interpreted under the federal National Labor Relations Act,
(ii) Seller has experienced no material labor difficulties
during the last five (5) years, (iii) there are
currently no labor disputes involving, by way of example,
strikes, work stoppages, slowdowns, picketing, or any other
forms or methods of interference with work or production, or any
other concerted action by Product Employees, (iv) there is
currently no existing or threatened grievance or other legal
action arising out of any collective bargaining agreement or
employment relationship of any kind or otherwise pending against
Seller, and (v) there are currently no charges or
proceedings before the National Labor Relations Board, or other
governmental agency.
(e) To Sellers Knowledge, all Product Employees are
authorized to work in the United States under the Immigration
Reform and Control Act of 1986, 8 U.S.C. § 1324a,
et seq.
(f) To Sellers Knowledge, no Product Employee intends
to terminate his or her employment with Seller,
(g) To Sellers Knowledge, (i) there are no
pending or threatened Actions (including unfair labor practice
and wage/hour charges) by any Product Employee against Seller,
and (ii) none of the Product Employees have been the
subject of any such actual or threatened proceedings within the
past two (2) years, except as set forth
on Schedule 4.9(g) of the Seller Disclosure
Schedule.
4.10 Compliance with Laws. Except
as set forth on Schedule 4.10 of the Seller
Disclosure Schedule:
(a) all Registrations employed in the Product Line Business
or necessary to the ongoing conduct of (i) the Product Line
Business, or (ii) to Sellers Knowledge, the
manufacture or supply of the Product for sale in the Territory,
are in full force and effect;
(b) except as set forth under Schedule 4.10(c)
of the Seller Disclosure Schedule, Seller and its conduct of the
Product Line Business are in material compliance with all
applicable Laws relating to the Product and the Purchased
Assets; and
(c) to Sellers Knowledge, no circumstances presently
exist which would reasonably be expected to lead to any loss of
or refusal to renew any Registrations employed in the Product
Line Business.
4.11 Regulatory Matters.
(a) All existing Registrations held by Seller as of the
date of this Agreement are set forth in
Schedule 1.1(j). Seller is the sole and exclusive
owner of the Registrations.
(b) To Sellers Knowledge, the Distribution of the
Product by Seller in the Territory has been conducted in
material compliance with the Registrations and all applicable
Laws, including the Act and the PDM Act.
(c) Except as set forth in Schedule 4.11(c) of
the Seller Disclosure Schedule, Seller has not received any
written or, to Sellers Knowledge, other notice of
proceedings from a Governmental Authority alleging that the
Product or any of the Purchased Assets or the ownership,
manufacturing, operation, storage, Distribution, warehousing,
packaging, labeling, handling
and/or
testing thereof is in material violation of any applicable Law.
(d) Seller has completed and filed all annual or other
reports required by the FDA in order to maintain the
Registrations to the extent required under the Product License
and Supply Agreement.
4.12 Government Product Contracts; Liability for
Cost and Pricing Data. (a) Seller has made
available to Purchaser true and correct copies of all Government
Product Contracts; provided that such copies may have
been redacted to prevent disclosure of information not related
to the Product.
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(b) Seller has made available to Purchaser true and correct
copies of Sellers Non-FAMP calculations and submissions,
with all supporting data, for the two (2) most recent
calendar quarters, as well as Sellers annual Federal
Ceiling Price (FCP) calculation and
submission for the FCP currently in effect, with all supporting
data.
(c) Seller has made available to Purchaser the FCP for
Product on Sellers FSS Contract.
(d) To Sellers Knowledge, there exists no claim for
Liability against Seller by any Governmental Authority as a
result of incomplete or Product-related defective pricing data
submitted to any Governmental Authority.
(e) Seller has made available to Purchaser all AMP and Best
Price related submissions regarding sales of the Product during
the period since the launch of the Product as submitted to the
Centers for Medicare and Medicaid Services.
4.13 Financial Statements. Each of
the consolidated financial statements (including, in each case,
any notes thereto) contained in Sellers SEC Filings, as
amended, supplemented or restated, if applicable, was prepared
in accordance with GAAP applied (except as may be indicated in
such filings and, in the case of unaudited quarterly financial
statements, as permitted by
Form 10-Q
under the Exchange Act) on a consistent basis during the periods
indicated (except as may be indicated in such filings), and
each, as amended, supplemented or restated, if applicable,
presented fairly, in all material respects, the consolidated
financial position of Seller as of the respective dates thereof
and the consolidated results of operations and cash flows of
Seller for the respective periods indicated therein (subject, in
the case of unaudited statements, to normal adjustments which,
individually or in the aggregate, are not reasonably expected to
have a Material Adverse Effect).
4.14 Warranties. Except as set
forth on Schedule 4.14 of the Seller Disclosure
Schedule, Seller has not made any warranties to its customers
with respect to the quality or absence of defects of the
Products which it has sold or have been sold on its behalf which
are in force as of the date hereof or with respect to which
claims are outstanding as of the date hereof. To Sellers
Knowledge, there are no claims pending, or threatened against
Seller with respect to the quality of, or existence of defects
in, any such Products and, to the Knowledge of Seller, there is
no legitimate basis for any such claim. Seller has made
available to Purchaser information which is accurate in all
material respects, regarding all returns of defective or expired
Products (other than Products damaged in transit), and all
credits and allowances for such defective or expired products
given or promised to customers during said period. Seller has
not paid or been required to pay or received a request or demand
for payment of any direct, incidental or consequential damages
to any Person in connection with any of such Products, except,
in each case, as would not reasonably be expected to have a
Material Adverse Effect.
4.15 Brokers, Etc. No broker,
investment banker, agent, finder or other intermediary acting on
behalf of Seller or under the authority of Seller, except for
UBS Securities LLC, is or will be entitled to any brokers
or finders fee or any other commission or similar fee
directly or indirectly in connection with any of the
Transactions.
4.16 Inventory and Equipment. To
Sellers Knowledge, (i) the Product Equipment and
Inventory are free from material defects, and (ii) the
Inventory is useable, saleable and merchantable in all material
respects.
4.17 Contracts.
(a) Other than the Pre-Existing Assigned Contracts, except
as set forth on Schedule 4.17(a) of the Seller
Disclosure Schedule, Seller is not a party to or bound by any
material Contract that is used primarily in or is necessary to
the operation or conduct of the Product Line Business.
(b) Except as set forth in Schedule 4.17(b) of
the Seller Disclosure Schedule,
(i) all Pre-Existing Assigned Contracts listed in
Schedule 1.1(b) are valid and binding on Seller and,
to Sellers Knowledge, are valid and binding on the other
party or parties thereto and in full force and effect;
(ii) Seller has performed all material obligations required
to be performed by it to date under the Pre-Existing Assigned
Contracts;
(iii) Seller is not (with or without the lapse of time or
the giving of notice, or both) in material breach or default in
any respect thereunder;
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(iv) to Sellers Knowledge, no third party to any
Pre-Existing Assigned Contract is (with or without the lapse of
time or the giving of notice, or both) in breach or default in
any respect thereunder; and
(v) Complete and correct copies of all Pre-Existing
Assigned Contracts listed in Schedule 1.1(b),
together with all modifications and amendments thereto and
material correspondence related thereto, have been made
available to Purchaser.
(c) With respect to those Assigned Contracts which Seller
does not deliver to Purchaser on or before Closing the written
consent of the parties to such Assigned Contracts regarding the
assignment to Purchaser, (i) the assignment of such
Assigned Contracts to Purchaser as contemplated by the
Transactions (X) is permitted under applicable Law,
(Y) shall not constitute a default or breach of under such
Assigned Contracts, and (ii) Seller has all rights and
consents necessary to effect such assignment to Purchaser as
contemplated by the Transactions, and (iii) upon such
assignment to Purchaser, Purchaser shall have all rights
necessary to exercise and enforce its rights (as assignee) under
such Assigned Contracts and to require performance of the other
parties to such Assigned Contracts.
4.18 Product Liability; Distributors;
Recalls. To Sellers Knowledge there is no
(X) fact relating to the Product that may impose upon the
Seller a duty to recall the Product or to warn customers of a
defect therein, or (Y) latent or overt design,
manufacturing or other defect in any Product. Except as set
forth on Schedule 4.18 of the Seller Disclosure
Schedule, Seller has not granted rights to any third party nor
appointed any third party as a licensee, distributor or
subdistributor of the Product. To Sellers Knowledge,
(i) there have been no recalls ordered by any Governmental
Authority with respect to the Product being sold by or on behalf
of Seller and (ii) each of the third parties appointed
by Seller as a licensee, distributor or subdistributor of the
Product identified on Schedule 4.18, if any, to
Sellers Knowledge, have obtained all approvals and
clearances necessary in order to market the Product in any and
all geographic areas in which they are marketed by or on behalf
of Seller.
4.19 Product Treatments; Product Returns;
Exporting and Manufacturing. Except as set forth
on Schedule 4.19, Seller has not offered any
promotional allowance (including, without limitation, any coupon
programs and
co-pay
assistance programs) to any customer nor has Seller or its
agents provided any customer-specific packaging or value added
services (other than displays) with respect to the Products.
Seller has processed all material returns or requests for
returns of the Products of which Seller is aware. Sellers
returns policy in effect prior to Closing and during the one
(1) year period prior to the Execution Date is attached
hereto as Schedule 4.19 of the Seller Disclosure
Schedule. During the one (1) year period prior to the
Execution Date, (i) Seller has processed returns consistent
with the foregoing returns policy, and (ii) except as would
not reasonably be expected to have a Material Adverse Effect,
(A) Seller has not refused to accept returns of any
Products and (B) no disputes arose with any customer of
Seller regarding any attempted return to Seller of any Product
sold by Seller. During the one (1) year period prior to the
Execution Date, no customer of Seller has refused to accept
further shipments of the Products. Seller does not have
outstanding any authorization to any of its customers to destroy
any of the Products in lieu of returning such product. Except as
set forth on Schedule 4.19 of the Seller Disclosure
Schedule, the Seller has not engaged in (i) any exporting
or manufacturing activities of or relating to any Product or the
Product Line Business, or (ii) Product Line Business
activities in Canada.
4.20 Customers, Suppliers and Third Party Service
Providers. Prior to the Execution Date, Seller
has provided Purchaser with a list of Sellers top ten
(10) customers by total sales of the Product for each of
the three (3) most recent calendar years (the
Customers). For purposes of this
Section 4.20, Customer shall mean any
entity contracting with Seller to purchase the Product whether
through written contract and without regard to the end user of
the goods in question. Since January 1, 2006, no supplier
or third party service provider of Seller providing goods or
services to the Product Line Business has indicated that it
shall stop, or materially decrease the rate of, providing
materials, products or services to Seller.
4.21 Medical Information. Prior to
the date hereof, Seller has provided Purchaser with access to
(a) a list of all serious adverse event reports and
periodic adverse event reports with respect to the Products that
have been filed by Seller since Sellers initial launch of
the Product, including any material correspondence or other
material documents relating thereto, complete copies of which
have been made available to Purchaser prior to the Effective
Date, (b) all payouts made by Seller since Sellers
initial launch of the Product to end-users in respect of claims
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relating to the Products and (c) all actual or threatened
claims made by end-users since Sellers initial launch of
the Product against Seller relating to the Product.
4.22 Disclaimer. EXCEPT AS
OTHERWISE EXPRESSLY PROVIDED IN THIS AGREEMENT, NONE OF THE
SELLER OR ITS REPRESENTATIVES MAKES OR HAS MADE ANY OTHER
REPRESENTATION OR WARRANTY, EXPRESS OR IMPLIED, WRITTEN OR ORAL,
AT LAW OR IN EQUITY, IN RESPECT OF THE PURCHASED ASSETS, ASSUMED
LIABILITIES, THE PRODUCT, THE PRODUCT INTELLECTUAL PROPERTY OR
THE PRODUCT LINE BUSINESS, INCLUDING ANY IMPLIED REPRESENTATION
OR WARRANTY WITH RESPECT TO (I) MERCHANTABILITY,
NON-INFRINGEMENT, SUITABILITY OR FITNESS FOR ANY PARTICULAR
PURPOSE, (II) THE OPERATION OF THE PRODUCT LINE BUSINESS BY
PURCHASER AFTER THE CLOSING IN ANY MANNER OTHER THAN AS USED AND
OPERATED BY SELLER OR, (III) THE PROBABLE SUCCESS OR
PROFITABILITY OF THE PRODUCT LINE BUSINESS AFTER THE CLOSING.
ARTICLE V
Representations
and Warranties of Purchaser
Purchaser represents and warrants to Seller as follows:
5.1 Organization. Purchaser is a
corporation duly organized and validly existing and in good
standing under the Laws of the place of its incorporation.
Purchaser has all requisite corporate power and authority to
own, lease and operate its properties and to carry on its
business as now being conducted.
5.2 Due Authorization. Purchaser
has all requisite corporate power and authority to execute,
deliver and perform its obligations under this Agreement and the
Other Agreements, and the execution and delivery of this
Agreement and the Other Agreements and the performance of all of
its obligations hereunder and thereunder have been duly
authorized by Purchaser and, to the extent required by Law,
contract or otherwise, its stockholders.
5.3 No Conflicts;
Enforceability. The execution, delivery and
performance of this Agreement and the Other Agreements by
Purchaser (a) are not prohibited or limited by, and will
not result in the breach of or a default under, any provision of
the certificate of incorporation or bylaws of Purchaser,
(b) assuming all of the consents, approvals, authorizations
and permits described in Section 5.5 have been
obtained and all the filings and notifications described in
Section 5.5 have been made and any waiting periods
thereunder have terminated or expired, conflict with any Law
applicable to Purchaser, and (c) does not conflict with,
result in a breach of, constitute (with or without due notice or
lapse of time or both) a default under, result in the
acceleration of obligations under, create in any party the right
to terminate, modify or cancel, or require any notice, consent
or waiver under, any material agreement or instrument binding on
Purchaser prior the Closing Date or any applicable order, writ,
injunction or decree of any court or Governmental Authority to
which Purchaser is a party or by which Purchaser is bound or to
which any of its Assets is subject, except for such prohibition,
limitation, default, notice, filing, permit, authorization,
consent, approval, conflict breach or default which would not
prevent or delay consummation by Purchaser of the Transactions.
This Agreement and the Other Agreements have been duly executed
and delivered by Purchaser, and constitute the legal, valid and
binding obligations of Purchaser, enforceable against Purchaser
in accordance with their respective terms, except as
enforceability may be limited or affected by applicable
bankruptcy, insolvency, moratorium, reorganization or other Laws
of general application relating to or affecting creditors
rights generally.
5.4 Litigation. There is no Action
pending or, to Purchasers knowledge, threatened, directly
or indirectly involving Purchaser (or to Purchasers
knowledge, any third party) that would prohibit, hinder, delay
or otherwise impair Purchasers ability to perform its
obligations hereunder or under the Other Agreements, including
the assumption of the Assumed Liabilities, would affect the
legality, validity or enforceability of this Agreement or the
Other Agreements, or prevent or delay the consummation of the
Transactions.
5.5 Consents. Except for the
requisite filings under the HSR Act and the expiration or
termination of the waiting period thereunder, any other
necessary premerger or competition filings, the letters to the
FDA contemplated by Sections 3.2(a)(iv) and
3.2(b)(iv), and as may be necessary as a result of any
facts or circumstances
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relating solely to Seller, no notice to, filing with,
authorization of, exemption by, or consent of, any Person,
including any Governmental Authority, is required for Purchaser
to consummate the Transactions.
5.6 Financing. Purchaser has
sufficient immediately available funds to pay, in cash, the
Purchase Price and all other amounts payable pursuant to this
Agreement and the Other Agreements or otherwise necessary to
consummate all the Transactions.
5.7 Brokers, Etc. No broker,
investment banker, agent, finder or other intermediary acting on
behalf of Purchaser or under the authority of Purchaser, except
for CitiGroup, is or will be entitled to any brokers or
finders fee or any other commission or similar fee
directly or indirectly in connection with any of the
Transactions.
ARTICLE IV
Covenants
Prior to Closing
6.1 Access to Information; Reporting;
Correspondence and Notices. Between the Execution
Date and the Closing Date, Seller shall, (i) afford
Purchaser and its Representatives access, during regular
business hours and upon reasonable agreed-upon times, to
Sellers personnel, personnel records (relating solely to
the Product Employees, if and to the extent permitted under
applicable Law, but in any event including date of hire, current
base salary, and severance for each Product Employee calculated
consistent with Schedule 9.1(a)(2)), and properties
pertaining primarily or exclusively to any of the Purchased
Assets, provided that such access shall not unreasonably
interfere with Sellers business and operations; and
(ii) copies of all Assigned Contracts or other
documentation constituting Purchased Assets. Without limiting
the generality of the foregoing, or being limited thereby,
Seller shall, at its own cost and expense, provide to Purchaser
on (1) the last Business Day of each calendar month
occurring prior to Closing, (2) daily for each of the five
(5) Business Days prior to Closing, and (3) on the
Closing Date, the following information and data
(Product Inventory Data):
(a) wholesale data comprised of (i) 852 reports from
each distribution services provider for the Product,
(ii) inventory balances as reported on 852 forms for each
wholesaler of the Product, (iii) morgue data
for each wholesaler of the Product, and
(iv) quarter-to-date
867 information for each wholesaler of the Product beginning
July 1, 2006 through the Closing Date;
(b) retail data comprised of (i) IMS prescription data
for the Product, and (ii) APROV study data for
the Product; and
(c) data relating to Inventory of Product held at ICS
including the lot numbers and expiration dates of such
Inventory, as well as Sellers out of pocket cost (without
markup and appropriately supported and documented in accordance
with GAAP) paid to Elan
and/or
Cardinal for all such units of Product.
Furthermore, Seller shall promptly provide Purchaser with
complete copies of any and all material correspondence, notices,
subpoenas, requests, demands, complaints or other written or
electronic communications received from, or sent by or behalf of
Seller to, (X) the third parties identified on
Schedule 2.5 and any other party to an Assigned
Contract, and (Y), to the extent such correspondence or other
communications relates to the Product or the Product Line
Business, to any of the top five (5) wholesalers of the
Product or the FDA, Health Canada, or any other Governmental
Authority, and (Z) any Person if it relates to any Material
Adverse Effect.
6.2 Conduct of the Product Line
Business. The Parties acknowledge that various
actions are desirable with respect to the smooth transition of
the Purchased Assets and Product Line Business from Seller to
Purchaser at the Effective Time and, consequently, Seller hereby
agrees to advise Purchaser from the date of this Agreement
through the Effective Time promptly following any material
developments or changes, if any, with respect to the Purchased
Assets or the Product Line Business. In addition, each of
Purchaser and Seller agree to advise the other Party promptly
upon becoming aware of any event, circumstance or development
arising subsequent to the date of this Agreement that would
result in any material breach of a representation, warranty or
covenant of such advising Party in this Agreement or that would
have the effect of making any representation or warranty of such
advising Party in this Agreement untrue or incorrect in any
material respect so as to cause the failure of any Closing
condition to be
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satisfied prior to or at the Closing. In addition to the
foregoing, to the extent consistent with applicable Law
throughout the period between the Execution Date and the
Effective Time:
(a) except as required by Law (including the Law of
fiduciary duties), neither Purchaser nor Seller shall take any
willful action reasonably likely to result in any material
representation or warranty made by such Party hereunder to
become untrue;
(b) subject to Section 6.3, Seller shall
exercise its reasonable best efforts to operate the Product Line
Business only in the ordinary course of business, consistent
with past practices and preserve intact in all material respects
the Purchased Assets and the Product Line Business, including,
to the extent that Seller currently has or currently purchases
wholesale data in support of the Product, Seller shall maintain
such wholesale data arrangements in all material respects;
(c) Seller shall not mortgage, pledge or subject the
Purchased Assets to any Encumbrance (other than Permitted
Encumbrances);
(d) Seller shall not enter into any Contracts (other than
Permitted Contracts) relating primarily or exclusively to the
Products or the Product Line Business;
(e) Seller shall not terminate Contracts that will
constitute Assigned Contracts at and as of the Effective Time;
(f) Seller shall use its commercially reasonable efforts to
maintain satisfactory relationships with and preserve the
goodwill of suppliers and customers providing products or
services primarily to or exclusively in connection with the
Product Line Business;
(g) Seller shall not transfer or grant any rights or
options in or to any of the Purchased Assets except for the
transfer of Inventory in the ordinary course of business
consistent with past practice;
(h) Seller shall not transfer or agree to transfer to any
third party any rights under any licenses, sublicenses or other
agreements with respect to any Product Intellectual Property;
(i) Seller shall pay all payables and Taxes relating to the
Product Line Business;
(j) Seller shall not fail to exercise any rights of renewal
with respect to any Assigned Contracts that by its terms would
otherwise expire and which Purchaser shall reasonably request
Seller to renew;
(k) Seller shall not (i) initiate any litigation or
arbitration actions or (ii) make any claims or demands for
breach against any party to any of the Assigned Contracts, or
threaten to take any such action;
(l) Seller shall not (i) enter into or modify any
employment agreement with a Product Employee; (ii) except
in the ordinary course consistent with past practice, increase
or improve wages or fringe benefits of Product Employees, or
(iii) promote, re-assign, transfer or change the job
description of any Product Employee; and
(l) Seller shall not agree to take any of the actions
specified in this Section 6.2.
6.3 Inventory. Seller shall
exercise its best efforts to reduce Inventory in commercial
(wholesale and retail) distribution channels to meet the
Wholesale Target and the Retail Target, provided,
however, that notwithstanding the foregoing
(i) Seller shall be entitled to ship Inventory after the
Execution Date and prior to Closing to the extent Seller
determines in its reasonable discretion that such shipments are
necessary to meet its ongoing cash requirements, and
(ii) such shipments shall not be a breach of this
Agreement; provided further Seller shall provide
Purchaser with advance written notice of any such shipments.
Seller shall give written notice to Purchaser of all Product
shipments made after the Execution Date promptly following each
shipment. Such notice shall set forth the quantity of the
Product shipped and, to the extent reasonably ascertainable, the
then current Inventory levels in commercial (wholesale and
retail) distribution channels.
6.4 Required Approvals and
Consents. As soon as reasonably practicable after
the Execution Date, the Parties shall make all filings required
to be made in order to consummate the Transactions, including
all filings under the HSR Act and any other necessary premerger
or competition filings in accordance with
Section 6.5.
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Seller shall also provide reasonable assistance with respect to
all filings that Purchaser elects to make which Purchaser, in
its reasonable discretion, deems legally necessary.
6.5 HSR Act.
(a) If required pursuant to applicable Law, each Party
shall file as soon as practicable, and in any event no later
than three (3) Business Days after the execution of a LOI
by the Parties, or if no LOI is executed by the Parties, after
the Execution Date except as mutually agreed otherwise, a
Notification and Report Form under the HSR Act with the United
States Federal Trade Commission and the Antitrust Division of
the United States Department of Justice, as well as any other
necessary premerger or competition filings. As deemed advisable,
each Party shall respond as promptly as practicable to any
inquiries or requests received from any Governmental Authority
in the Territory for additional information or documentation.
Each Party shall (i) promptly notify the other Party of any
communication to that Party or its Affiliates from any
Governmental Authority and, subject to applicable Law, permit
the other Party or the other Partys counsel to review in
advance any proposed written communication to any of the
foregoing; (ii) not participate, or permit its Affiliates
to participate, in any substantive meeting or discussion with
any Governmental Authority in respect of any filings,
investigation or inquiry concerning this Agreement unless it
consults with the other Party in advance and, to the extent
permitted by such Governmental Authority in the Territory, gives
the other Party the opportunity to attend and participate
thereat; and (iii) subject to applicable Law and any other
reasonable confidentiality obligations of the disclosing Party,
furnish the other Party with copies of all correspondence,
filings, and communication (and memoranda setting forth the
substance thereof) (including documents submitted as attachments
to each Partys Notification and Report Form under the HSR
Act) between such Party (its affiliates, and its respective
Representatives) on the one hand, and any Governmental Authority
or members of their respective staffs on the other hand, with
respect to this Agreement. The responsibility for any required
HSR Act filing fees shall be split 50/50 between Purchaser and
Seller.
(b) In furtherance and not in limitation of the other
covenants of the Parties contained herein, Purchaser shall have
the right, but not the obligation, to seek to remedy any
material competition concerns that any Governmental Authority
may have with respect to the consummation of the Transactions.
If any administrative, judicial or legislative Action is
instituted (or threatened to be instituted) challenging the sale
and purchase of the Purchased Assets or any of the Transactions
as violative of any anti-competition Law, Purchaser may, but
shall not be required to, elect to contest and resist any such
Action, and to have vacated, lifted, reversed or overturned any
decree, judgment, injunction or other order that is in effect
and that restricts, prevents or prohibits the consummation of
the Transactions. In the event Purchaser elects not to seek to
remedy any such competition concerns of a Governmental Authority
after being given notice thereof, Seller may terminate this
Agreement by giving notice of termination to Purchaser. Seller
shall cooperate in a commercially reasonable manner with any
efforts of Purchaser to remedy any such competition concerns of
a Governmental Authority.
6.6 Proxy Statement; Seller Stockholders
Meeting.
(a) Proxy Statement. As promptly as
practicable after the Execution Date, Seller shall prepare and
file with the SEC a proxy statement relating to Seller
Stockholders Meeting (together with any amendments thereof
or supplements thereto, the Proxy Statement).
Seller, after consultation with Purchaser, will use commercially
reasonable efforts to respond to any comments made by the SEC
with respect to the Proxy Statement and to make any further
filings in connection therewith Seller in its reasonable
discretion deems necessary or appropriate. Purchaser shall
furnish all information as Seller may reasonably request in
connection with such actions and the preparation of the Proxy
Statement. As promptly as practicable after the clearance of the
Proxy Statement by the SEC, Seller shall mail the Proxy
Statement to its stockholders. Subject to
Section 6.7, the Proxy Statement shall include the
Seller Recommendation. Seller will notify Purchaser, promptly
after it receives notice thereof, of any request by the SEC for
amendment of the Proxy Statement or comments thereon and
responses thereto or requests by the SEC for additional
information. Seller shall supply Purchaser with copies of all
written correspondence between Seller or any of its
Representatives, on the one hand, and the SEC or the SECs
staff or any other governmental officers, on the other hand,
with respect to the Proxy Statement or the Transactions;
provided, however, that nothing herein shall obligate
Seller to disclose any written information submitted to the SEC
for which Seller has obtained confidential treatment thereof
from the SEC. If at any time prior to the Effective Time, any
event or circumstance relating to Purchaser or any Affiliate of
Purchaser, or their respective Representatives,
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should be discovered by Purchaser which should be set forth in
an amendment or a supplement to the Proxy Statement, Purchaser
shall promptly inform Seller. If at any time prior to the
Effective Time, any event or circumstance relating to Seller or
any Subsidiary of Seller, or their respective Representatives,
should be discovered by Seller which should be set forth in an
amendment or a supplement to the Proxy Statement, Seller shall
promptly inform Purchaser. All documents that Seller is
responsible for filing in connection with the Transactions will
comply as to form and substance in all material respects with
the applicable requirements of the Exchange Act and other
applicable Laws.
(b) Information Supplied. The Proxy
Statement is Sellers document and Seller shall be and
remain solely responsible for its contents. All documents that
Seller is responsible for filing with the SEC in connection with
the Transactions will comply as to form in all material respects
with the applicable requirements of the Exchange Act and will
not contain any untrue statement of a material fact, or omit to
state any material fact required to be stated therein in order
to make the statements therein, in light of the circumstances
under which they were made, not misleading.
(c) Seller Stockholders
Meeting. Subject to this Section 6.6,
Seller shall mail the Proxy Statement to its stockholders and
call and hold a meeting of its stockholders (the Seller
Stockholders Meeting) in accordance with
Sellers bylaws and applicable Law as promptly as
practicable following the date on which the Proxy Statement is
cleared by the SEC for the purpose of obtaining the approval of
the Required Seller Stockholders. Subject to Sellers
fiduciary duties and applicable Law, Seller will use its
commercially reasonable efforts to solicit from its stockholders
proxies in favor of the adoption and approval of this Agreement
and the Transactions, and will take all other reasonable action,
if any, deemed necessary by Seller to secure the approval of its
stockholders (by vote or consent) required by applicable Law,
Sellers certificate of incorporation and bylaws, each as
amended to date, and, if applicable, all Contracts binding on
Seller. The Proxy Statement will contain the Seller
Recommendation; provided, however, that no director or
officer of Seller shall be required to violate any fiduciary
duty or other requirement imposed by Law in connection therewith.
(d) Convertible Notes. Prior to Seller
Stockholders Meeting, Seller shall mail to each of the
holders of the Convertible Notes a notice of redemption pursuant
to Section 3.04 of the Indenture entered into by Seller and
dated as of November 26, 2002. Without limiting the
foregoing or being limited thereby, Seller shall have redeemed
or converted all of the Convertible Notes by the earlier of the
Closing Date or the Outside Date. Seller shall not disperse or
otherwise distribute to any of its stockholders any proceeds
from any sale of Sellers assets prior to (i) the
redemption or conversion of all of the Convertible Notes and
(ii) repayment in full of any indebtedness owed to
Purchaser by Seller.
(e) No Restriction. Nothing in this
Section 6.6 shall be deemed to prevent Seller or the
board of directors of Seller from taking any action they are
permitted or required to take under, and in compliance with,
Section 6.6 or are required to take under applicable
Law. Nothing contained in this Agreement shall give Purchaser,
directly or indirectly, the right to control or direct
Sellers or its Subsidiaries operations prior to the
Effective Time.
6.7 No Negotiation. Between the
Execution Date and the Closing Date, Seller agrees it shall not,
and shall cause its Affiliates and Representatives not to,
directly or indirectly, take any action to (i) solicit,
initiate or facilitate any Acquisition Proposal, (ii) as to
any such Acquisition Proposal, participate in any way in
discussions or negotiations with, or furnish any non-public
information to, any Person that has made an Acquisition Proposal
or (iii) enter into any agreement with respect to any
Acquisition Proposal; provided, however, that, at any
time prior to the Closing Date, Seller shall, following the
provision of notice to Purchaser, be permitted to:
(a) participate in any discussions or negotiations with,
and provide any non-public information (other than any
confidential information of Purchaser or any non-public
financial or other material terms of this Agreement) to, any
Person in response to an Acquisition Proposal by any such
Person, if the board of directors of Seller determines that
there is a reasonable likelihood that such Acquisition Proposal
could lead to a Superior Proposal;
(b) if Seller has received an Acquisition Proposal from a
third party and the board of directors of Seller determines that
such Acquisition Proposal constitutes a Superior Proposal,
effect a change in the Seller Recommendation or enter into an
agreement with respect to such Acquisition Proposal;
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(c) effect a change in the Seller Recommendation if the
board of directors of Seller determines that doing so is
consistent with its fiduciary duties to Sellers
stockholders under applicable Law; and
(d) take and disclose to Sellers stockholders a
position with respect to any tender offer or exchange offer by a
third party or amend or withdraw such a position in accordance
with
Rule 14d-9
and
Rule 14e-2
of the Exchange Act.
6.8 Notifications. Between the
Execution Date and the Closing Date, Seller, on the one hand,
and Purchaser, on the other hand, shall promptly notify the
other Party in writing of any fact, change, condition,
circumstance or occurrence or nonoccurrence of any event of
which it is aware that will or is reasonably likely to result in
any of the conditions set forth in Article VII
becoming incapable of being satisfied; provided, however,
that the delivery of any notice pursuant to this
Section 6.8 shall not limit or otherwise affect the
remedies available hereunder to the Party receiving such notice.
6.9 Product Packaging.
(a) Following the Execution Date, Purchaser shall exercise
its reasonable best efforts to obtain its own NDC number for the
Product and develop and obtain governmental approval of its own
proposed packaging for the Product for use by Purchaser upon
Closing, in each case at Purchasers sole cost and expense
(including, without limitation, any fees, expenses or costs
associated with converting at Purchasers request existing
Inventory to reflect Purchasers packaging for the Product).
(b) In order ensure the Parties compliance with Drug
Enforcement Administration guidelines and requirements and to
facilitate a more efficient transfer of the Product and Product
Line Business to Purchaser upon Closing, Seller shall, in
cooperation with Purchaser, use commercially reasonable efforts
(i) to arrange, effective upon a date mutually agreed upon
by the Parties, for Elan and Cardinal to appropriately hold and
store in unlabeled bottles (e.g., bright stock) at
their respective manufacturing sites all production of Product
currently scheduled to be produced and shipped to ICS between
execution and Closing; and (ii) upon appropriate lead time,
to arrange for Elan and Cardinal to label such Product using
labeling made available by Purchaser but retain possession of
such packaged Product until the date of Closing. In the event
this Agreement is terminated, Purchaser shall pay for all
reasonable costs and expenses to label with Sellers label
all such Purchaser labeled Product.
6.10 Further Assurances; Further Documents.
(a) As of the Execution Date, each of the Parties shall use
its commercially reasonable efforts, in the most expeditious
manner practicable, (i) to satisfy or cause to be satisfied
all the conditions precedent that are set forth in
Article VII, as applicable to each of them,
(ii) to cause the Transactions to be consummated, and
(iii) without limiting the generality of the foregoing, to
obtain all consents and authorizations of third parties and to
make all filings with, and give all notices to, third parties
that may be necessary or reasonably required on its part in
order to consummate the Transactions.
(b) Each of Purchaser and Seller shall, and shall cause its
respective Affiliates to, at the request of another Party,
execute and deliver to such other Party all such further
instruments, assignments, assurances and other documents as such
other Party may reasonably request in connection with the
carrying out of this Agreement and the Transactions.
ARTICLE VII
Conditions
to Closing
7.1 Conditions Precedent to Obligations of
Purchaser and Seller. The respective obligations
of Purchaser and Seller to consummate the Transactions on the
Closing Date are subject to the satisfaction or waiver (in
accordance with Section 12.7) at or prior to the
Closing Date of the following conditions:
(a) Litigation. No preliminary or
permanent injunction or other order has been issued by any court
or by any Governmental Authority, body or authority which
enjoins, restrains, prohibits or makes illegal pursuant to
applicable Law the Transactions on the Closing Date.
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(b) HSR Act. Any waiting period (and any
extension thereof) under the HSR Act applicable to the
Transactions has expired or been terminated.
(c) Stockholder Approval. The Required
Seller Stockholders shall have approved stockholder resolutions
authorizing Seller to consummate the Transactions.
7.2 Conditions Precedent to Purchasers
Obligations. Purchasers obligations to
consummate the Transactions shall be subject to the fulfillment
of each of the following additional conditions, any one or more
of which may be waived, at Purchasers sole discretion, in
writing by Purchaser:
(a) Representations and Warranties. The
representations and warranties of Seller contained in
Article IV shall be true and correct in all material
respects as of the Execution Date and true and correct in all
material respects as of the Effective Time as though made on and
as of the Effective Time (except that those representations and
warranties which address matters only as of a particular date
need only be true and correct as of such date).
(b) Performance. Seller shall have
performed and complied in all material respects with each of the
covenants, agreements and obligations Seller is required to
perform under this Agreement on or before the Closing.
(c) Consents. All Consents to the
Assignments shall have been duly executed and delivered to
Purchaser; provided that with respect to each of Sellers
Contracts with ICS or Stericycle (formerly Universal Solutions
International Inc.) relating to the Product, if, prior to
Closing Purchaser shall have entered into its own contracts with
such third parties regarding Purchasers conduct of the
Product Line Business following Closing, Seller shall be
relieved of its obligation to obtain Consent to Assignment of
such Contracts.
(d) Officers Certificate. Purchaser
shall have received a certificate executed by a duly elected,
qualified and acting officer of Seller certifying to the
satisfaction of the conditions set forth in
Sections 7.2(a) and (b).
(e) Other Agreements. Seller shall have
duly executed and delivered to Purchaser the Other Agreements.
(f) Convertible Notes. Seller shall have
redeemed or converted all of the Convertible Notes.
7.3 Conditions Precedent to Sellers
Obligations. Sellers obligation to
consummate the Transactions shall be subject to the fulfillment
of each of the following additional conditions, any one or more
of which may be waived, at Sellers sole discretion, in
writing by Seller:
(a) Representations and Warranties. Each
of the representations and warranties of Purchaser contained in
Article V shall be true and correct in all material
respects as of the Execution Date and as of the Effective Time
as though made on and as of the Effective Time (except that
those representations and warranties which address matters only
as of a particular date need only be true and correct as of such
date).
(b) Performance. Purchaser shall have
performed and complied in all material respects with each of the
covenants, agreements and obligations Purchaser is required to
perform under this Agreement on or before the Closing.
(c) Officers Certificate. Seller
shall have received a certificate executed by a duly elected,
qualified and acting officer of Purchaser certifying to the
satisfaction of the conditions set forth in
Sections 7.3(a) and (b).
(d) Other Agreements. Purchaser shall
have duly executed and delivered the Other Agreements to Seller.
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ARTICLE VIII
Additional
Covenants
8.1 Confidentiality; Publicity.
(a) The terms of the Confidentiality Agreement shall apply
to any information provided to Seller or Purchaser pursuant to
this Agreement.
(b) The Parties shall jointly agree upon the necessity and
content of any press release in connection with the execution of
this Agreement and the matters contemplated hereby as well as
the Closing of the Transactions hereunder. Any other
publication, news release or other public announcement by a
Party relating to this Agreement or to the performance hereunder
shall first be reviewed and consented to in writing by the other
Party; provided, however, that notwithstanding any
contrary term contained in the Confidentiality Agreement,
(i) any disclosure that is required by Law as advised by
the disclosing Partys counsel may be made without the
prior written consent of the other Party, provided a copy of
such disclosure is provided to the other Party prior to any such
legally required disclosure, and (ii) any Party may issue a
press release or public announcement if the contents of such
press release or public announcement have previously been made
public other than through a breach of this Agreement by the
issuing Party, without the prior written consent of the other
Party. To the extent practicable, the disclosing Party shall
give at least three (3) Business Days advance notice of any
such legally required disclosure to the other Party, and such
other Party may provide any comments on the proposed disclosure
during such period and if not practicable, such lesser
practicable period, if any. Notwithstanding any contrary term
contained in the Confidentiality Agreement, to the extent that
either Party determines that it or the other Party is required
to file or register this Agreement, a summary thereof or a
notification thereof to comply with the requirements of an
applicable stock exchange, Exchange regulation, New York Stock
Exchange regulation or Nasdaq regulation or any Governmental
Authority, including without limitation the SEC, such Party
shall give at least two (2) Business Days advance written
notice of any such required disclosure to the other Party. Prior
to making any such filing, registration or notification, the
Parties shall reach mutual agreement with respect thereto
regarding any confidential treatment request. The Parties shall
cooperate, each at its own expense, in such filing, registration
or notification, including without limitation such confidential
treatment request, and shall execute all documents reasonably
required in connection therewith.
8.2 Availability of Records. After
the Closing, Seller, on the one hand, and Purchaser, on the
other hand, shall make available to each other Party and its
Affiliates and Representatives during normal business hours when
reasonably requested, all Product Records in its possession and
shall preserve all such information, records and documents until
the later of: (i) six (6) years after the Closing;
(ii) the expiration of all statutes of limitations for
assessing or collecting Taxes for periods ending on or prior to
the Closing and periods including the Closing Date, including
extensions thereof applicable to Seller or Purchaser; or
(iii) the required retention period under any applicable
Laws for all such information, records or documents (it being
understood that the Parties shall not be required to provide any
Tax Returns to any Person, other than as required by applicable
Laws). Purchaser and Seller shall also make available to each
other during normal business hours, when reasonably requested,
personnel responsible for preparing or maintaining information,
records and documents, in connection with Tax matters,
governmental contracts, litigation or potential litigation, each
as it relates to the Product, Product Line Business, Purchased
Assets or Assumed Liabilities prior to the Closing Date (with
respect to Seller) or from and after the Closing Date (with
respect to Purchaser), including product liability and general
insurance liability.
8.3 Notification of
Customers. Promptly after the Closing, Purchaser
and Seller shall jointly notify all wholesale distributors of
the Product (a) of the transfer of the Purchased Assets to
Purchaser, (b) that all purchase orders for the Product
received by Seller or any of its Affiliates prior to the Closing
Date but not shipped prior to 11:59 p.m. eastern time on or
prior to the Business Day immediately preceding the Closing Date
will be transferred to Purchaser (provided that to the
extent that any purchase order cannot be so transferred, Seller
and Purchaser shall cooperate with each other to ensure that
such purchase order is filled and that Purchaser receives the
same economic benefit and assumes the same Liability associated
with filling such purchase order as if such purchase order had
been so transferred), and (c) that all purchase orders for
the Product received after the Closing Date should be sent to
the Persons and addresses as directed by Purchaser.
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8.4 Product Returns, Rebates and Chargebacks.
(a) Product Returns.
(i) Purchaser shall be responsible for all Product returns
from and after the Closing Date other than with respect to any
returns of the Product sold prior to the Effective Time for
which Seller shall be and remain responsible for processing
after the Closing Date. A list of all lot numbers of Product
sold by Seller since the launch of the Product and to the
Closing Date is attached at Schedule 8.4(a). The
Parties shall use, and cause any third party return processing
service providers to use, the foregoing list to determine which
Party shall be responsible for returns of a particular lot of
Product.
(ii) The Party responsible for the returns of the Product
in a given lot number
and/or NDC
shall be responsible for processing such returns as well as be
financially responsible for such returns. Seller and Purchaser
shall issue joint instructions in writing to third parties from
which Product returns may be expected hereunder and otherwise
reasonably cooperate with one another to help ensure Product
returns are made in an appropriate manner.
(iii) Notwithstanding any provision herein to the contrary,
Purchaser and its Affiliates shall not take any action with the
intention of encouraging or otherwise affirmatively causing
Sellers customers and distributors to return Products.
(b) Government Rebates.
(i) Seller shall be responsible for all claims for all
rebates pursuant to any governmental rebate program
(Government Rebates) for Products dispensed
prior to the Effective Time; provided that Sellers
responsibility with respect to such Government Rebates shall
terminate 180 days following the Closing Date (the
Rebate Tail Period) and, after the
termination of the Rebate Tail Period, Purchaser shall be
responsible for legally and accurately calculated Government
Rebates owed by Seller for Products dispensed prior to the
Effective Time (to the extent not previously paid by Seller)
and, in addition, for the avoidance of doubt, Purchaser shall be
responsible for all Government Rebates for Products dispensed
after the Effective Time. Purchaser acknowledges that Seller
will require certain information from Purchaser in order to
calculate the Government Rebates for Product bearing NDC numbers
of Seller or any of its Affiliates. Seller acknowledges that
Purchaser will require certain information from Seller to meet
its obligations with regard to pricing and calculating
Government Rebates. Accordingly, the Parties agree that, from
and after the Closing Date until the date which is one
(1) calendar year after the expiration date of the last lot
of Product produced with any NDC number of Seller, each Party
shall reasonably cooperate with the other Party in connection
with appropriately submitting to the Centers for Medicare and
Medicaid Services, and in providing to the other Party, the
following information: (a) the Best Price for each Product
identified by NDC number, (b) the average
manufacturer price (AMP) (as defined
under the Social Security Act, 42 U.S.C.
§ 1396r-8(k)(1))
for each Product identified by the NDC number, (c) all data
used by Purchaser or Seller to calculate the AMP and Best Price
for each Product identified by NDC number, and (d) any
additional pricing
and/or
claims data or other information related to such Medicaid issues
reasonably requested by the other Party. Without limiting the
generality of the foregoing, or being limited thereby, Purchaser
shall make all appropriate filings (even after Closing, as
necessary) with the Centers for Medicare and Medicaid Services
in regard to all pre-Closing sales of Product, including any
filings covering Sellers sales of Product in a partial
calendar quarter period leading up the Closing Date.
(ii) Purchaser shall pay or reimburse Seller for legally
and accurately calculated Government Rebates owed by Seller to
any Governmental Authority (to the extent not previously paid by
Seller) following the termination of Government Rebate Tail
Period; provided, that the Parties acknowledge that
Government Rebates are billed on a calendar quarter basis and,
to the extent that Purchasers reimbursement obligations
under this Section 8.4(b)(ii) commence following the
first (1st) day of any calendar quarter, Purchaser shall
reimburse Seller in an amount equal to the total amount of the
Government Rebates billed to Seller for such quarter, multiplied
by a fraction, the numerator of which shall be the number of
days elapsed during such quarter for which Purchaser has a
reimbursement obligation under this Section 8.4(b),
and the denominator of which shall be the number of days elapsed
during such calendar quarter. Seller shall submit an invoice to
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Purchaser for the amount due from Purchaser to Seller hereunder
within ten (10) Business Days after receipt by Seller of
any claim for a Government Rebate for which Purchaser may be
responsible under this
Section 8.4(b). Purchaser shall make all
payments due under this Section 8.4(b) to Seller
upon receipt by Purchaser of invoices from Seller that describe
the requested payments in reasonable detail. IN NO EVENT SHALL
SELLER OR ANY GOVERNMENTAL AUTHORITY CLAIM, AND PURCHASER SHALL
NOT BE OBLIGATED TO REIMBURSE SELLER FOR OR PAY ANY GOVERNMENTAL
AUTHORITY FOR ANY GOVERNMENT REBATES THAT ARE NOT OWED BY SELLER
OR ARE NOT BASED UPON LEGALLY AND ACCURATELY CALCULATED
INFORMATION SUBMITTED TO GOVERNMENTAL AUTHORITIES BY SELLER.
(iii) If Purchaser disputes in good faith any Government
Rebate claimed by Seller to be owed by Purchaser to Seller under
any invoice submitted to Purchaser pursuant to
Section 8.4(b)(ii), Purchaser shall provide notice
to Seller within ten (10) Business Days of receipt of such
invoice requesting that Seller notify the applicable
Governmental Authority that Purchaser disputes such claim and
the reasonable basis therefor. Seller shall, to the extent not
part of the Purchased Assets, provide to Purchaser, upon
Purchasers reasonable request, copies of any documents and
records evidencing the original Government Rebate claims and any
resubmission of such claims and data relating to unit Government
Rebate calculations that are reasonably necessary to enable
Purchaser to resolve such disputed amount. Purchaser shall be
responsible for managing the dispute and amount owed under any
such disputed Government Rebate, and Seller shall provide
reasonable assistance to Purchaser in its dispute thereof;
provided that Purchaser shall reimburse Seller for any
and all reasonable costs and expenses incurred by Seller as a
result of Purchasers dispute of such Government Rebate.
(iv) Notwithstanding the other provisions of this
Section 8.4, the Parties acknowledge that the VA
National Acquisition Center must approve the addition of the
Product to Purchasers Federal Supply Schedule
(FSS) Contract and the removal of the Product
from Sellers FSS Contract before the responsibility of
processing such chargebacks is transferred from Seller to
Purchaser. Until such approval is obtained, Seller shall
continue to be responsible for processing the FSS chargebacks on
Purchasers behalf, at Purchasers sole costs and
expense (with Purchaser promptly paying such costs and expenses
as they become due or promptly reimbursing Seller for such costs
as paid by Seller), in each case in a manner consistent with
this Agreement. Seller shall provide Purchaser with all
information reasonably related to the Product and the prices
thereof that Purchaser reasonably requires in order to comply
with applicable rules and regulations relating to P.L. 102-585
as it relates to the FSS. When requested, such information shall
be provided by Seller to Purchaser as promptly as practicable.
(v) Schedule 8.4(b) sets forth the
Best Price (as defined at 42 U.S.C.
§ 1396r-8(c)(1)(C))
and AMP reported by Seller for the Product for the two most
recently ended calendar quarters.
(c) Commercial Rebates. Seller shall be
responsible for all claims for all commercial rebates for
Products sold prior to the Effective Time; provided that
Sellers responsibility with respect to such commercial
rebates shall terminate upon termination of the Rebate Tail
Period and thereafter Purchaser shall be responsible for
commercial rebates (to the extent not already paid by Seller)
for Products sold prior to the Effective Time and, in addition,
for the avoidance of doubt, Purchaser shall be responsible for
all claims for commercial rebates for Products sold after the
Effective Time. Schedule 8.4(c) hereto contains a
list of all commercial rebate agreements, commercial chargeback
agreements and Medicare Part D agreements in which the
Product is included (Commercial Rebate
Agreements). Seller and Purchaser agree that Purchaser
shall continue to honor all such Commercial Rebate Agreements
following the Effective Time; provided, however, that
Seller shall exercise its reasonable best efforts to terminate
each such Commercial Rebate Agreement promptly following the
Closing and no later than ten (10) Business Days thereafter
and shall notify Purchaser in writing of such terminations in
accordance with the applicable agreement. Upon termination of
such agreements, Sellers Liability for such rebates and
chargebacks shall cease. Seller shall be responsible at
Sellers sole cost and expense for the processing, payment,
administration, support, and termination of all such Commercial
Rebate Agreements. To the extent that Purchaser processes
commercial rebates and chargebacks that are the responsibility
of Seller, Seller shall reimburse Purchaser within thirty
(30) days of receipt of Purchasers invoices for the
same together with appropriate documentation supporting such
claim, including without limitation, the lot numbers, NDC
number, the party/customer filing for the rebates and
chargebacks and identification of the contract under which the
Product in question with purchased. Similarly, to the extent
that Seller
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processes commercial rebates and chargebacks for Product sold
under Sellers NDC by or on behalf of Purchaser after the
Effective Time, Purchaser shall reimburse Seller within thirty
(30) days of receipt of Sellers invoices for the
same. Any disputes with respect to such amounts due (and the
related costs of any Accountants incurred in connection
therewith, if any) shall be resolved in the manner set forth in
Section 2.8(d).
(d) Credits Shelf Stock
Adjustments. Notwithstanding the foregoing,
Purchaser and Seller agree that (i) Seller shall not be
responsible for credits shelf stock adjustments to the extent
resulting from price decreases initiated by Purchaser after
Closing and (ii) any such payments by Seller shall be made
on the terms and conditions comparable to Sellers rebate
obligations as of the Closing with respect to each commercial
customer and shall be based on Sellers terms of agreement
with the respective contract. To the extent that Seller
processes such claims, Purchaser shall reimburse Seller within
thirty (30) days of receipt of invoices that describe the
requested payments in reasonable detail.
8.5 Accounts Receivable. The
Parties acknowledge and agree that all Accounts Receivable are
and shall after Closing remain the property of Seller and
Sellers Affiliates and shall be collected by Seller or
Sellers Affiliates subsequent to the Closing. In the event
that, subsequent to the Closing, Purchaser or Purchasers
Affiliates receives any payments from any obligor with respect
to an Account Receivable outstanding on the Closing Date, then
Purchaser shall within thirty (30) days of receipt of such
payment remit the full amount of such payment to Seller. In the
case of the receipt by Purchaser of any payment from any obligor
of both Seller and Purchaser then, unless otherwise specified by
such obligor, such payment shall be applied first to amounts
owed to Purchaser with the excess, if any, remitted to Seller.
In the event that, subsequent to the Closing, Seller or
Sellers Affiliates receives any payments from any obligor
with respect to an account receivable of Purchaser for any
period after the Closing Date, then Seller shall within thirty
(30) days of receipt of such payment remit the full amount
of such payment to Purchaser. In the case of the receipt by
Seller of any payment from any obligor of both Seller and
Purchaser then, unless otherwise specified by such obligor, such
payment shall be applied first to amounts owed to Seller with
the excess, if any, remitted to Purchaser.
8.6 Regulatory Matters.
(a) From and after the Closing Date, Purchaser, at its
cost, shall be solely responsible and liable for (i) taking
all actions, paying all fees and conducting all communication
with the appropriate Governmental Authority required by Law in
respect of the Registrations, including preparing and filing all
reports (including adverse drug experience reports) with the
appropriate Governmental Authority (whether the Product is sold
before or after transfer of such Registrations),
(ii) taking all actions and conducting all communication
with third parties with respect to Product sold pursuant to such
Registrations (whether sold before or after transfer of such
Registrations), including responding to all complaints in
respect thereof, including complaints related to tampering or
contamination, and (iii) investigating all complaints and
adverse drug experiences with respect to Product sold pursuant
to such Registrations (whether sold before or after transfer of
such Registrations).
(b) From and after the Closing Date, Seller promptly (and
in any event within the time periods required by Law) shall
notify Purchaser within three (3) Business Days if Seller
receives a complaint or a report of an adverse drug experience
with respect to the Product, but within twenty-four
(24) hours if Seller receives a complaint or a report of a
serious adverse drug experience. In addition, Seller shall
cooperate with Purchasers reasonable requests and use
commercially reasonable efforts to assist Purchaser in
connection with the investigation of and response to any
complaint or adverse drug experience related to the Product sold
by Seller.
(c) From and after the Closing Date, Purchaser, at its
cost, shall be solely responsible and liable for conducting all
voluntary and involuntary recalls of units of the Product sold
pursuant to such Registrations (whether sold before or after
transfer of such Registrations), including recalls required by
any Governmental Authority and recalls of units of the Product
sold by Seller deemed necessary by Seller in its reasonable
discretion; provided, however, that Seller shall promptly
reimburse Purchaser for all reasonable expenses and costs
incurred by Purchaser relating to recalls (whether voluntary or
required by any Governmental Authority) relating to Product sold
by or on behalf of Seller prior to the Closing, including
without limitation the costs of notifying customers, the costs
associated with shipment of such recalled Product, the price
paid for such Product, and reasonable credits extended to
customers in connection with the recall. Seller promptly shall
notify Purchaser in the event that a recall of the Product sold
by Seller is necessary.
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8.7 Website Information. As soon as
practicable following the Closing Date, but in no event less
than ten (10) Business Days following the Closing Date,
Seller shall remove all references to the Product from the
Product Information and Research and
Development sections of its website; provided upon
request of Purchaser, Seller shall place a link to website(s)
designated by Purchaser.
8.8 Tax Matters.
(a) Seller and Purchaser shall reasonably cooperate with
one another to lawfully minimize all Transfer Taxes, and
resulting Transfer Taxes, if any, shall be split by Purchaser
and Seller 50/50. Seller and Purchaser shall cooperate in
preparing and timely filing all Tax Returns and other
documentation relating to such Transfer Taxes as may be required
by applicable Tax Law.
(b) Seller and Purchaser hereby waive compliance with any
bulk sales Laws (including any requirement to
withhold any amount from payment of the Purchase Price)
applicable to the sale to Purchaser of the Purchased Assets and
the Inventory by Seller.
8.9 Government Product Contracts.
(a) After the Effective Time, Purchaser shall honor and
perform all Liabilities of Seller arising after the Effective
Time under and pursuant to each Government Product Contract with
respect to supplying the Product to the applicable party
pursuant to such Government Product Contract until such time as
the VA permits Purchaser add the Product to its FSS Contract.
Seller agrees that, except as otherwise required by applicable
Law, after the Effective Time it will not take any action with
respect to any Government Product Contract that would, to
Sellers Knowledge, extend the term of such Government
Product contract with respect to the Product or otherwise
adversely affect Purchaser or the Product Line Business, without
the prior consent of Purchaser. Seller may enter into a separate
agreement with such government party, provided that such
agreements do not contain any provisions relating to the Product
or the Product Line Business.
(b) Seller shall provide Purchaser with all information and
data reasonably requested by Purchaser necessary for Purchaser
to add the Product to its FSS Contract to the extent not
included in the Purchased Assets. Seller shall terminate the
rights and obligations of Seller with respect to the Product
under each such government product contract, to the extent
permitted by the terms thereof and to the extent permitted by,
and in accordance with, applicable Law, as soon as reasonably
practicable after notification from Purchaser that the Product
has been added to Purchasers FSS Contract.
(c) Seller shall provide Purchaser all data related to
Sellers sales of Product necessary for Purchaser to
calculate a new Federal Ceiling Price under the Veterans Health
Care Act, 38 U.S.C. § 8126.
8.10 Insurance. Seller shall
maintain, at its expense, general liability insurance together
with product liability coverage for sales of the Product made
prior to the Closing Date, which shall be written by A-rated
insurance carriers as rated by A.M. Best Company, having a
limit of not less than Ten Million Dollars ($10,000,000) in
the aggregate, for a period of three (3) years following
the Closing Date. Such insurance shall name each of King, King
R&D and their respective Affiliates as additional named
insureds. Seller shall provide to Purchaser thirty
(30) days prior written notice of any cancellation or
change in any of the foregoing coverage. Prior to Closing and
thereafter upon request of Purchaser, Seller shall provide to
Purchaser certificates of insurance evidencing the foregoing
coverage.
8.11 Product Promotion.
(a) Purchaser shall exercise commercially reasonable
efforts to promote the Product during the Royalty Term.
Commercially reasonable efforts to promote shall mean (except to
the extent the FDA, the U.S Drug Enforcement Administration or a
court of competent jurisdiction finally and conclusively
determines that Purchaser is legally prohibited from doing so):
(a) for the period during the Royalty Term from the Closing
Date through December 31, 2008, that Purchaser shall cause
to be performed a minimum of 15,000 PDEs per calendar month
(pro-rated for partial months); and (b) for the period
during the Royalty Term from January 1, 2009 through
December 31, 2009, that Purchaser shall cause to be
performed a minimum of 10,000 PDEs per month (pro-rated for
partial months); provided that, in each case, such PDEs
shall be calculated on a quarterly basis. Thereafter, during the
remainder of
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the Royalty Term, commercially reasonable efforts shall mean at
least the same degree of effort as exercised in the promotion of
Purchasers other products of a similar market size, patent
life and similar commercial opportunity.
(b) Purchaser shall exercise commercially reasonable
efforts to explore alternate formulations and derivations of the
Product which utilize the same single active ingredient as the
Product.
(c) During the Royalty Term, Purchaser shall not market in
the Territory for once-daily administration any controlled
release solid oral dosage formulation containing morphine and
its salts as its sole active ingredient, other than Product.
(d) Purchaser confirms that it has received a copy of the
Product License and Supply Agreement. Purchaser agrees that it
shall be bound by the provisions of the Product License and
Supply Agreement and shall perform in accordance with its terms
all the obligations which by the terms of the Product License
and Supply Agreement are required to be performed by Seller.
Without limiting the foregoing, Purchaser acknowledges the
foregoing covenant shall continue throughout the duration of the
Royalty Term.
8.12 Advisory Fees, etc. Seller
will provide for the transfer, on the Closing Date, to UBS
Securities LLC (who is an intended third-party beneficiary of
this paragraph) a cash amount sufficient to pay in full all
amounts due and payable to UBS Securities LLC in connection with
the Transactions.
ARTICLE IX
Employee
Matters
9.1 Employee Offers.
(a) Effective as of the Effective Time, Purchaser or an
Affiliate of Purchaser shall offer to employ, on an at-will
basis, each of the Product Employees listed on
Schedule 9.1(a)(1) (provided that such list shall in
no event exceed eighty-seven (87) individuals, and after
review of the employment records and/or interview of each listed
individual (which in no event shall occur prior to HSR
approval), Purchaser, in its discretion, may decline to offer
employment to any Product Employee for valid, job-related
reasons and provided further that Purchaser, in its discretion,
will determine its staffing needs and therefore the aggregate
number of Product Employees to be offered employment and the
tasks to be performed by them) so long as (i) each such
employee is currently performing his or her regular tasks during
what have been customarily scheduled work hours for its
salespersons; (ii) as of the Effective Time, each such
employee is then able to perform the essential functions of the
positions to be offered by Purchaser, with or without reasonable
accommodation, and (iii) each such employee is already
subject to or, prior to hire by Purchaser, signs a trade secret,
confidentiality, work for hire, non-compete, and any
other similar agreement or agreements proffered by and with
Purchaser, with such employment, if accepted, to commence as of
the Effective Time. Such offers of employment shall be delivered
to applicable Product Employees at least five (5) Business
Days prior to the Closing or as soon as practicable thereafter
but, in any event, prior to the Closing. The Product Employees
who become employed by Purchaser are herein referred to as the
Hired Employees.
(b) On or before the effective date of hire by Purchaser,
Seller shall terminate the employment of each Hired Employee and
all Hired Employees shall cease participation in all Seller
Plans, subject to the terms of such plans.
(c) All Product Employees on Schedule 9.1(a)(1)
who receive no employment offers from Purchaser will remain
employees of Seller, or, at Sellers option, Seller will
sever their employment. If such employment severance occurs
within ten (10) Business Days following the Closing Date,
Seller shall treat such Product Employees as terminated
employees under the severance pay policy attached hereto as
Schedule 9.1(a)(2), and, to the extent they are
eligible for severance pay under such policy, will, at
Sellers discretion, offer them severance pay consistent
with Schedule 9.1(a)(2). Purchaser agrees to reimburse
Seller for the amount of severance pay paid out to such severed
Product Employees only to the extent (i) Purchaser has not
offered employment to such Product Employees pursuant to
Section 9.1(a) above, and (ii) such severance
pay is properly paid out in accordance with the severance pay
policy attached hereto as Schedule 9.1(a)(2), including
without limitation that each such severance pay-eligible Product
Employee submits to Seller and Purchaser a valid, binding,
signed release of all possible legal claims against Seller and
Purchaser in a form and in substance acceptable to Seller and
Purchaser. Seller shall otherwise remain solely liable for the
severance of such severed Product Employees.
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(d) Seller, at the request of Purchaser, shall enforce, now
or in the future, any non-competition, non-solicitation,
confidentiality, trade secret or like agreements between Seller
and any of its employees, including any Product Employees, who
have any confidential knowledge or information about the Product
Line Business or have had any role in Distribution of the
Product.
9.2 Benefits.
(a) Seller shall pay out to each Hired Employees any and
all vacation pay, personal pay, and sick leave benefits earned
but not yet used as of the date on which each such employee
terminates employment with Seller in order to commence
employment with Purchaser.
(b) Seller shall retain responsibility for and continue to
pay all workers compensation, medical and dental and
similar plan benefits for each Hired Employee with respect to
claims incurred by such Hired Employee or his or her covered
dependents under the Seller Plans prior to the Closing Date and
beyond the Closing Date, to the extent the benefit-triggering
event occurred prior to Closing and Liability continues after
Closing. Without limiting the generality of
Section 9.2, Seller and its Affiliates shall retain
sole responsibility for all Liabilities in respect of
continuation coverage of health insurance under
Section 4980B of the Code or Part 6 of Title I of
ERISA or other similar state or local law to Product Employees
and any other current and former employees of Seller and their
Affiliates and their eligible dependents with respect to
qualifying events (as defined in Section 4980B
of the Code) occurring prior to the Closing Date. Purchaser
shall be responsible for satisfying all obligations under
Section 4980B of the Code or Part 6 of Title I of
ERISA or other similar state or local law with respect to any
Hired Employee with respect to qualifying events
occurring on or after the Closing Date.
9.3 WARN Act. Purchaser shall be
responsible for all Liabilities, obligations, costs, claims,
proceedings and demands, under the WARN Act, or any state plant
closing or notification law, or similar Law in other
jurisdictions, arising out of, or relating to, (i) in
respect of Product Employees, the failure of Purchaser to offer
employment to Product Employees in accordance with
Section 9.1(a), or (ii) in respect of Hired
Employees, any actions taken by Purchaser or its Affiliates on
or after the Closing Date; so long as any information provided
by Seller and relied upon by Purchaser is accurate, and with the
further understanding, that Purchaser shall not be responsible
for any such Liabilities, obligations, costs, claims,
proceedings and demands to or in respect of any employees of
Seller other than the Product Employees.
9.4 Employee Information. Following
the Execution Date, Seller shall use commercially reasonable
efforts to provide Purchaser with all information and data
reasonably requested by Purchaser in connection with
Purchasers rights and obligations under this
Article IX, including exchanging information and
data relating to employee employment history and benefits and
employee benefit plan coverages (except to the extent prohibited
by applicable Law).
ARTICLE X
Indemnification
10.1 Indemnification by Seller. For
purposes of determining the existence and amount of
Sellers indemnification obligations hereunder, a breach of
Sellers representations or warranties shall be determined
without regard to any limitation or qualification as to
materiality or Material Adverse Effect (or similar concept) set
forth in such representation or warranty. Seller shall indemnify
Purchaser and its Affiliates and their respective, officers,
directors, employees, stockholders, agents and Representatives
against, and hold them harmless from, any Losses, to the extent
arising from:
(a) any breach of any representation or warranty of Seller
contained in this Agreement or Sellers Officers
Certificate;
(b) any pre-Closing activities of Seller, including but not
limited to Sellers returns pertaining to sales of the
Product before the Closing or termination of this Agreement;
(c) any breach of any covenant of Seller contained in this
Agreement;
(d) any Excluded Liabilities; and
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(e) any fees, expenses or other payments incurred or owed
by Seller to any brokers, financial advisors or comparable other
Persons retained or employed by it in connection with the
Transactions.
10.2 Indemnification by
Purchaser. Purchaser shall indemnify Seller and
its Affiliates and their respective officers, directors,
employees, stockholders, agents and Representatives against, and
agrees to hold them harmless from, any Losses, to the extent
arising from or in connection with or otherwise with respect to:
(a) any breach of any representation or warranty of
Purchaser contained in this Agreement or Purchasers
Officers Certificate;
(b) any breach of any covenant of Purchaser contained in
this Agreement;
(c) any Assumed Liability; and
(d) any fees, expenses or other payments incurred or owed
by Purchaser to any brokers, financial advisors or other
comparable Persons retained or employed by it in connection with
the Transactions.
10.3 Procedures.
(a) In order for a Party (the Indemnified
Party) to be entitled to any indemnification provided
for under this Agreement in respect of, arising out of or
involving a claim made by any Person against the Indemnified
Party (a Third Party Claim), such Indemnified
Party must notify the indemnifying party (the
Indemnifying Party) in writing (and in
reasonable detail) of the Third Party Claim within
fifteen (15) Business Days after receipt by such
Indemnified Party of notice of the Third Party Claim;
provided, however, that failure to give such notification
shall not affect the indemnification provided hereunder except
to the extent the Indemnifying Party shall have been actually
prejudiced as a result of such failure (except that the
Indemnifying Party shall not be liable for any expenses incurred
during the period in which the Indemnified Party failed to give
such notice). Thereafter, the Indemnified Party shall deliver to
the Indemnifying Party, within five Business Days after
the Indemnified Partys receipt thereof, copies of all
notices and documents (including court papers) received by the
Indemnified Party relating to the Third Party Claim.
(b) If a Third Party Claim is made against an Indemnified
Party, the Indemnifying Party shall be entitled to participate
in the defense thereof and, if it so chooses, to assume the
defense thereof with counsel selected by the Indemnifying Party.
If the Indemnifying Party assumes such defense, the Indemnified
Party shall have the right to participate in the defense thereof
and to employ counsel, at its own expense, separate from the
counsel employed by the Indemnifying Party, it being understood
that the Indemnifying Party shall control such defense. The
Indemnifying Party shall be liable for the reasonable fees and
expenses of counsel employed by the Indemnified Party for any
period during which the Indemnifying Party has not assumed the
defense thereof (other than during any period in which the
Indemnified Party shall have failed to give notice of the Third
Party Claim as provided above). If the Indemnifying Party
chooses to defend or prosecute a Third Party Claim, all
Indemnified Parties shall cooperate in the defense or
prosecution thereof. Such cooperation shall include the
retention and (upon the Indemnifying Partys request) the
provision to the Indemnifying Party of records and information
that are reasonably relevant to such Third Party Claim, and
making employees and Representatives available on a mutually
convenient basis to provide additional information and
explanation of any material provided hereunder or other matters
reasonably related to such Third Party Claim. Whether or not the
Indemnifying Party assumes the defense of a Third Party Claim,
the Indemnified Party shall not admit any liability with respect
to, or settle, compromise or discharge, such Third Party Claim
without the Indemnifying Partys prior written consent
(which consent shall not be unreasonably withheld). If the
Indemnifying Party assumes the defense of a Third Party Claim,
the Indemnified Party shall agree to any settlement, compromise
or discharge of a Third Party Claim that the Indemnifying Party
may recommend and that by its terms obligates the Indemnifying
Party to pay the full amount of the Losses in connection with
such Third Party Claim, which releases the Indemnified Party
completely in connection with such Third Party Claim and that
would not otherwise materially adversely affect the Indemnified
Party.
(c) In the event any Indemnified Party should have a claim
against any Indemnifying Party under Section 10.1 or
10.2 that does not involve a Third Party Claim being
asserted against or sought to be collected from such Indemnified
Party, the Indemnified Party shall deliver notice of such claim
with reasonable promptness to the Indemnifying Party, but in any
event not later than five (5) Business Days after the
Indemnified Party determines
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that it has or could have a claim to indemnification hereunder,
stating the amount of Loss, if known, and method of computation
thereof, and containing a specific reference to the provisions
of this Agreement in respect of which such right of
indemnification is claimed or arises. The failure by any
Indemnified Party so to notify the Indemnifying Party shall not
relieve the Indemnifying Party from any indemnification
obligation that it may have to such Indemnified Party under
Section 10.1 or 10.2, as applicable, except
to the extent that the Indemnifying Party is prejudiced by such
failure. If the Indemnifying Party disputes that it has an
indemnification obligation with respect to such claim, the
Indemnifying Party shall deliver notice of such dispute with
reasonable promptness and the Indemnifying Party and the
Indemnified Party shall proceed in good faith to negotiate a
resolution of such dispute for a period of
thirty (30) days following the receipt by the
Indemnified Party of such dispute notice. If the Indemnified
Party and the Indemnifying Party have not resolved such dispute
during such time period through good faith negotiations, such
dispute shall be resolved by litigation in an appropriate court
of competent jurisdiction or other mutually agreeable
non-judicial dispute resolution mechanism.
10.4 Certain Limitations on Indemnification
Obligations. Purchaser shall not be entitled to
receive any indemnification payments under this
Article X unless and until the aggregate amount of
all indemnifiable Losses incurred by Purchaser equals One
Million Five Hundred Thousand Dollars ($1,500,000) (the
Basket Amount), whereupon Purchaser shall be
entitled to receive in full indemnity payments for all such
Losses that exceed the Basket Amount; provided that the
maximum aggregate amount of indemnification payments under this
Article X to which Purchaser shall be entitled shall
not exceed Forty Million Dollars ($40,000,000); provided
further that Purchaser shall not be permitted to submit a
claim for indemnification if aggregate Losses with respect to
such claim are less than Two Thousand Five Hundred Dollars
($2,500).
10.5 Set-Off. Any indemnifiable
Losses to which Purchaser is entitled pursuant to the provisions
of this Article X shall be satisfied as follows: first,
such Losses shall be satisfied from the Escrow Account pursuant
to the terms of the Escrow Agreement; second, subject to the
provisions of this Article X, such Losses shall be
set-off against Royalties then accrued but not paid to Seller
hereunder to the extent no amounts remain in the Escrow Account;
and third, to the extent, and only to the extent, unable to be
satisfied from the Escrow Account and the Royalties, directly
from Seller. Any payment for indemnifiable Losses determined to
be due to Purchaser pursuant to this Article X from
the Escrow Account, or any set-off against Royalties due and
payable to Seller for indemnifiable Losses determined to be due
to Purchaser pursuant to this Article X, shall be
made within ten (10) days following the determination
(in accordance with this Article X) of the
amount of such indemnifiable Losses due and payable to Purchaser.
10.6 Survival. Sellers
indemnification obligation hereunder shall survive sixteen
(16) months after the Closing Date, provided,
however, that Sellers indemnification obligation for
Sellers breach of Sections 4.2, 4.4 or
4.9 shall survive for a period of thirty (30) months
after the Closing Date. Notwithstanding the foregoing,
indemnification obligations of an Indemnifying Party shall
survive the foregoing termination dates with respect to matters
that the Indemnified Party has in good faith provided notice to
the Indemnifying Party prior to the applicable termination date
pursuant to Section 10.3 above, and the Indemnifying
Partys obligation shall be tolled until such matters are
definitively resolved.
ARTICLE XI
Termination
and Survival
11.1 Termination.
(a) This Agreement may be terminated:
(i) at any time before the Closing Date by mutual written
consent of Purchaser and Seller; or
(ii) by either Party, in writing, if the Transactions have
not been consummated on or before December 31, 2006 (the
Outside Date), provided that such
failure is not due to the failure of the Party seeking to
terminate this Agreement to comply in all material respects with
its obligations under this Agreement; or
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(iii) by either Party if the adoption of this Agreement by
the Required Seller Stockholders shall not have been obtained at
Sellers Stockholders Meeting (or at any adjournment
thereof) by reason of the failure to obtain the required
vote; or
(iv) by either Party, if a material breach of any provision
of this Agreement has been committed by the other Party, such
breach has not been waived and such breach is not cured within
sixty (60) days after written notice thereof.
(b) This Agreement may be terminated by Seller before
Closing, in writing,if:
(i) (A) any representation or warranty of Purchaser
set forth in this Agreement shall have become untrue in any
material respect or Purchaser has materially breached any
covenant or agreement of Purchaser set forth in this Agreement,
and (B) such breach or misrepresentation is not capable of
being cured prior to the Outside Date;
(ii) a material breach of any provision of this Agreement
has been committed by Purchaser, such breach has not been waived
by Seller and such breach is not cured by Purchaser within ten
(10) days after written notice thereof or, in the
reasonable determination of Seller, is incapable of being cured
by Purchaser; or
(iii) the board of directors of Seller determines that an
Acquisition Proposal is a Superior Proposal, in which case
Seller must, within two (2) days thereafter, provide
Purchaser written notice of such determination.
(c) This Agreement may be terminated by Purchaser before
Closing, in writing, if:
(i) (A) any representation or warranty of Seller set
forth in this Agreement shall have become untrue in any material
respect or Seller has materially breached any covenant or
agreement of Seller set forth in this Agreement, and
(B) such breach or misrepresentation is not capable of
being cured prior to the Outside Date;
(ii) a material breach of any provision of this Agreement
has been committed by Seller and such breach is not cured by
Seller within ten (10) days after written notice thereof
or, in the reasonable determination of Purchaser, is incapable
of being cured by Seller; or
(iii) if, prior to obtaining the approval of this Agreement
by the Required Seller Stockholders (A) Seller has failed
to include the Seller Recommendation in the Proxy Statement or
(B) the board of directors of Seller approves or recommends
an Acquisition Proposal to Sellers stockholders or
approves or recommends that its stockholders tender their shares
of Sellers common stock in any tender offer or exchange
offer that is an Acquisition Proposal; or
(iv) Purchaser has received written notice from Seller
indicating that Sellers board of directors has determined
that an Acquisition Proposal is a Superior Proposal.
11.2 Procedure and Effect of
Termination.
(a) Upon termination of this Agreement by Seller or
Purchaser pursuant to Section 11.1, written notice
thereof shall forthwith be given to the other Party and this
Agreement shall terminate forthwith and become void and there
shall be no Liability or obligation on the part of the Parties
or their respective Representatives. Termination of this
Agreement shall terminate all outstanding obligations and
liabilities between the Parties arising from this Agreement
except those described in: (i) Section 8.1,
this Article XI and Article XII;
(ii) the Confidentiality Agreement; and (iii) any
other provisions of this Agreement which by their nature are
intended to survive any such termination.
(b) In the event that this Agreement is terminated by
Seller pursuant to (i) Section 11.1(b)(iii) or
(ii) by Purchaser pursuant to Sections 11.1(c)(iii)
or (iv), Seller shall pay King a fee equal to Twelve
Million Dollars ($12,000,000) (the Termination
Fee) by wire transfer of immediately available funds
to an account designated by King in writing. The Termination Fee
shall be paid promptly, but in no event later than three
(3) Business Days after the date of receipt by Seller of
such wiring instructions. Receipt of the Termination Fee shall
be Purchasers sole and exclusive remedy against Seller for
accepting a Superior Proposal.
(c) In the event that this Agreement is terminated by
Seller pursuant to Section 11.1(b)(i) or
Section 11.1(b)(ii) then, in addition to any other
remedies available to Seller under this Agreement, Purchaser
shall pay to Seller within
A-37
two (2) Business Days after the receipt of a notice
therefor an amount equal to Sellers reasonable
out-of-pocket
expenses in connection with the negotiation, execution and
delivery of this Agreement and the actions taken in furtherance
of the consummation of this Agreement, by wire transfer of
immediately available funds to an account designated by Seller
in writing.
(d) In the event that this Agreement is terminated by
Purchaser pursuant to Section 11.1(c)(i) or
Section 11.1(c)(ii) then, in addition to any other
remedies available to Purchaser under this Agreement, Seller
shall pay to King within two (2) Business Days after the
receipt of a notice therefor an amount equal to Purchasers
reasonable
out-of-pocket
expenses in connection with the negotiation, execution and
delivery of this Agreement and the actions taken in furtherance
of the consummation of this Agreement, by wire transfer of
immediately available funds to an account designated by King in
writing.
ARTICLE XII
Miscellaneous
12.1 Assignment; Binding
Effect. This Agreement shall be binding upon and
inure to the benefit of the Parties hereto and their respective
successors and assigns; provided, however, that
Purchaser may not sell, transfer, assign, license, sublicense,
delegate, pledge or otherwise dispose of, whether voluntarily,
involuntarily, by operation of Law or otherwise, this Agreement
or any of its rights or obligations under this Agreement without
the prior written consent of Seller, which consent may be
granted, withheld or conditioned at Sellers sole and
absolute discretion; provided, further
notwithstanding the foregoing Purchaser may assign its
rights under this Agreement as security to one or more financial
institutions providing financing (not in relation to the Closing
of the Transactions contemplated hereunder) to Purchaser and may
be assigned pursuant to the terms of the relevant security
agreement; provided, further, that any permitted
assignment shall protect Sellers rights under this
Agreement.
12.2 Expenses. Except as otherwise
specified herein, each Party shall bear its own expenses with
respect to the Transactions.
12.3 Notices. All notices,
requests, claims, demands and other communications hereunder
shall be in writing and shall be deemed to have been duly given
(a) when received if delivered personally, (b) upon
receipt, if sent by registered or certified mail (postage
prepaid, return receipt requested) and (c) the day after it
is sent, if sent for next-day delivery to a domestic address by
overnight mail or courier, to the Parties at the following
addresses:
If to Seller, to:
Ligand Pharmaceuticals Incorporated
10275 Science Center Drive
San Diego, California 92121
Attention: General Counsel
with a copy sent concurrently to:
Latham & Watkins LLP
12636 High Bluff Drive, Suite 400
San Diego, California 92130
Attn: Scott Wolfe
Attn: Faye Russell
If to Purchaser, to:
King Pharmaceuticals, Inc.
501 Fifth Street
Bristol, Tennessee 37620
Attention: General Counsel, Legal Affairs
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with copies sent concurrently to:
King Pharmaceuticals, Inc.
400 Crossing Boulevard
Bridgewater, New Jersey 08807
Attention: General Counsel, Legal Affairs
Reed Smith LLP
Princeton Forrestal Village
136 Main Street, Suite 250
Princeton, New Jersey 08540
Attn: Andres Liivak
provided, however, that if any Party shall have
designated a different address by notice to the others, then to
the last address so designated.
12.4 Severability. If any term,
provision, covenant or restriction of this Agreement is held by
a court of competent jurisdiction or other authority to be
invalid, void, unenforceable or against its regulatory policy
such determination shall not affect the enforceability of any
others or of the remainder of this Agreement.
12.5 Entire Agreement. This
Agreement may not be amended, supplemented or otherwise modified
except by an instrument in writing signed by all of the Parties
hereto. This Agreement, the Other Agreements and the
Confidentiality Agreement contain the entire agreement of the
Parties hereto with respect to the Transactions, superseding all
negotiations, prior discussions and preliminary agreements made
prior to the Execution Date
12.6 No Third Party
Beneficiaries. Except as otherwise set forth
under Article IX, this Agreement is solely for the
benefit of the Parties hereto and their respective Affiliates
and no provision of this Agreement shall be deemed to confer
upon any third parties any remedy, claim, Liability,
reimbursement, claim of action or other right in excess of those
existing without reference to this Agreement.
12.7 Waiver. The failure of any
Party to enforce any condition or part of this Agreement at any
time shall not be construed as a waiver of that condition or
part, nor shall it forfeit any rights to future enforcement
thereof.
12.8 Governing Law;
Jurisdiction. Except for federal Laws referenced
in this Agreement, and except as superseded by federal Law, this
Agreement (including any claim or controversy arising out of or
relating to this Agreement) shall be governed by the law of the
State of New York without regard to conflict of law principles
that would result in the application of any Law other than the
Law of the State of New York. All Actions arising out of or
relating to this Agreement shall be heard and determined
exclusively in the Court of Chancery of the State of Delaware,
and any appellate court from any thereof, in any Action arising
out of or relating to this Agreement, the Other Agreements, the
Transactions or for recognition or enforcement of any judgment
relating thereto, and each of the Parties hereby irrevocably and
unconditionally (a) agrees not to commence any such Action
except in such courts, (b) agrees that any claim in respect
of any such Action may be heard and determined in the Court of
Chancery of the State of Delaware, (c) waives, to the
fullest extent it may legally and effectively do so, any
objection which it may now or hereafter have to the laying of
venue of any Action in the Court of Chancery of the State of
Delaware, and (d) waives, to the fullest extent permitted
by Law, the defense of an inconvenient forum to the maintenance
of such Action in the Court of Chancery of the State of
Delaware. Each of the Parties hereto agrees that a final
judgment in any such Action shall be conclusive and may be
enforced in other jurisdictions by suit on the judgment or in
any other manner provided by Law. Each Party to this Agreement
irrevocably consents to service of process in the manner
provided for notices in Section 12.4. Nothing in
this Agreement will affect the right of any Party to this
Agreement to serve process in any other manner permitted by Law.
12.9 Injunctive
Relief. Notwithstanding anything to the contrary
in this Agreement, either Party will have the right to seek
temporary injunctive relief in any court of competent
jurisdiction as may be available to such Party under the Laws
applicable in such jurisdiction with respect to any matters
arising out of the other Partys performance of its
obligations under this Agreement. Either Party agrees that in
the event the other Party institutes an appropriate Action
seeking injunctive/equitable relief for specific performance
under this Agreement, the Party seeking such relief shall not be
required to provide the other Party with service of process of a
complaint and
A-39
summons under the procedures set forth in any Canadian or other
non-United States judicial process or system. Under such
circumstances, the Party seeking such relief need only provide
the other Party with two copies of a true, correct and lawfully
issued summons and complaint, via Federal Express (priority
delivery).
12.10 Headings. The headings of the
sections and subsections of this Agreement are inserted for
convenience only and shall not be deemed to constitute a part
hereof.
12.11 Counterparts. This Agreement
may be executed manually, electronically in
Adobe®
PDF file format, or by facsimile by the Parties, in any number
of counterparts, each of which shall be considered one and the
same agreement and shall become effective when a counterpart
hereof shall have been signed by each of the Parties and
delivered to the other Party.
12.12 Schedules. Purchaser agrees
that any disclosure by Seller in any Schedule attached hereto
shall not establish any threshold of materiality or concede the
materiality of any matter or item disclosed.
12.13 Construction. The language in
all parts of this Agreement shall be construed, in all cases,
according to its fair meaning. The Parties acknowledge that each
Party and its counsel have reviewed and revised this Agreement
and that any rule of construction to the effect that any
ambiguities are to be resolved against the drafting Party shall
not be employed in the interpretation of this Agreement.
* * * * * * * * * *
A-40
IN WITNESS WHEREOF, the Parties hereto have caused this
Agreement to be executed by their respective duly authorized
officers as of the date first above written.
LIGAND PHARMACEUTICALS INCORPORATED
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By:
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/s/ Henry
F. Blissenbach
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Name:
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Henry F. Blissenbach
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KING PHARMACEUTICALS, INC.
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By:
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/s/ Brian
A. Markison
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KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC.
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By:
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/s/ Brian
A. Markison
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A-41
ANNEX B
Opinion of UBS Securities LLC
[LETTERHEAD OF UBS SECURITIES LLC]
September 6, 2006
The Board of Directors
Ligand Pharmaceuticals Incorporated
10275 Science Center Drive
San Diego, California 92121
Dear Members of the Board:
We understand that Ligand Pharmaceuticals Incorporated, a
Delaware corporation (Ligand), is considering a
transaction whereby King Pharmaceuticals, Inc., a Tennessee
corporation (King), and its wholly owned subsidiary,
King Pharmaceuticals Research and Development, Inc., a Delaware
corporation (King R&D), will purchase from
Ligand all of its rights in and to certain finished dosage
strengths of the once-daily oral dosage microparticulate
formulation developed by Elan Corporation (Elan)
currently marketed by Ligand as
Avinza®,
other dosage strengths, reformulations or derivations thereof
and any other product sold or distributed under the
Avinza®
trademark (the Product) and certain related assets
(such rights and assets to be purchased from Ligand, the
Purchased Assets). Pursuant to the terms of the
Purchase Agreement, dated as of September 6, 2006 (the
Purchase Agreement), among King, King R&D and
Ligand, Ligand will transfer to King and King R&D the
Purchased Assets and specified liabilities (the
Transaction) for initial consideration of
$312.75 million (the Initial Consideration),
subject to adjustment as specified in the Purchase Agreement,
consisting of $265.0 million in cash and the assumption of
Ligands payment obligation of $47.75 million to
Organon Pharmaceuticals USA Inc. (or reimbursement to Ligand of
such amount to the extent paid by Ligand prior to the closing of
the Transaction). The Purchase Agreement also provides that,
beginning on the later of the closing date of the Transaction or
January 1, 2007 until November 25, 2017, King will
make royalty payments to Ligand based on the Net Sales (as
defined in the Purchase Agreement) of the Product in accordance
with a specified schedule (the Royalty Payments and,
together with the Initial Consideration, the Aggregate
Consideration). The terms and conditions of the
Transaction are more fully set forth in the Purchase Agreement.
You have requested our opinion as to the fairness, from a
financial point of view, to Ligand of the Aggregate
Consideration to be received by Ligand in the Transaction.
UBS Securities LLC (UBS) has acted as financial
advisor to Ligand in connection with the Transaction and will
receive a fee for its services, a portion of which is payable in
connection with this opinion and a significant portion of which
is contingent upon consummation of the Transaction. UBS in the
past has provided, and currently is providing, investment
banking services to Ligand unrelated to the proposed
Transaction, for which UBS received and expects to receive
compensation. In the past, UBS has provided investment banking
services to King unrelated to the proposed Transaction, for
which UBS received compensation. In the ordinary course of
business, UBS, its successors and affiliates may hold or trade,
for their own accounts and the accounts of their customers,
securities of Ligand and King and, accordingly, may at any time
hold a long or short position in such securities.
Our opinion does not address the relative merits of the
Transaction as compared to other business strategies or
transactions that might be available with respect to the
Purchased Assets or Ligands underlying business decision
to effect the Transaction. Our opinion does not constitute a
recommendation to any stockholder of Ligand as to how such
stockholder should vote or act with respect to the Transaction.
At your direction, we have not been asked to, nor do we, offer
any opinion as to the terms, other than the Aggregate
Consideration to the extent expressly specified herein, of the
Purchase Agreement or any related documents or the form of the
Transaction. In rendering this opinion, we have assumed, with
your consent, that (i) Ligand, King and King R&D will
comply with all material terms of the Purchase Agreement and
related documents and (ii) the Transaction will be
consummated in accordance with the terms of the Purchase
Agreement and related documents without any adverse waiver or
The Board of Directors
Ligand Pharmaceuticals Incorporated
September 6, 2006
Page 2
amendment of any material term or condition thereof. We have
also assumed that all governmental, regulatory or other consents
and approvals necessary for the consummation of the Transaction
will be obtained without any material adverse effect on the
Purchased Assets, Ligand, King or the Transaction.
In arriving at our opinion, we have, among other things:
(i) reviewed certain publicly available business and
financial information relating to the Purchased Assets and King;
(ii) reviewed certain internal financial information and
other data relating to the Purchased Assets that were provided
to us by the management of Ligand and not publicly available,
including financial forecasts and estimates (including forecasts
and estimates as to Net Sales anticipated by the management of
Ligand to be achieved by King) prepared by the management of
Ligand; (iii) conducted discussions with members of the
senior management of Ligand concerning the Purchased Assets;
(iv) reviewed publicly available financial and stock market
data with respect to certain companies we believe to be
generally relevant; (v) compared the financial terms of the
Transaction with the publicly available financial terms of
certain other transactions we believe to be generally relevant;
(vi) reviewed the Purchase Agreement and certain related
documents; and (vii) conducted such other financial
studies, analyses and investigations, and considered such other
information, as we deemed necessary or appropriate. At your
direction, we contacted third parties to solicit indications of
interest in a possible transaction with Ligand and held
discussions with certain of these parties prior to the date
hereof.
In connection with our review, with your consent, we have not
assumed any responsibility for independent verification of any
of the information provided to or reviewed by us for the purpose
of this opinion and have, with your consent, relied on such
information being complete and accurate in all material
respects. In addition, with your consent, we have not made any
independent evaluation or appraisal of any assets (including the
Purchased Assets) or liabilities (contingent or otherwise) of
Ligand, nor have we been furnished with any such evaluation or
appraisal. With respect to the financial forecasts and estimates
(including forecasts and estimates as to Net Sales) referred to
above, we have assumed, at your direction, that they have been
reasonably prepared on a basis reflecting the best currently
available estimates and judgments of the management of Ligand as
to the future performance of the Purchased Assets and as to Net
Sales. In addition, we have assumed, with your approval, that
the forecasts and estimates as to Net Sales referred to above
will be achieved at the times and in the amounts projected. We
also have relied, at your direction, without independent
verification or investigation, upon the assessments of the
management of Ligand as to the Product and the risks associated
therewith (including the potential impact of drug competition).
Our opinion is necessarily based on economic, monetary, market
and other conditions as in effect on, and the information
available to us as of, the date hereof.
Based upon and subject to the foregoing, it is our opinion that,
as of the date hereof, the Aggregate Consideration to be
received by Ligand in the Transaction is fair, from a financial
point of view, to Ligand.
This opinion is provided for the benefit of the Board of
Directors in connection with, and for the purpose of, its
evaluation of the Transaction.
Very truly yours,
UBS SECURITIES LLC
B-2
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The
Board of Directors recommends a vote FOR Items 1, 2 and 3.
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Please
Mark Here
for Address
Change or
Comments
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o
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SEE REVERSE SIDE |
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FOR |
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AGAINST |
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ABSTAIN |
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1. To approve the sale of all or
substantially all of our assets under
Delaware law through the sale of our
rights in and to AVINZA® (morphine
sulfate extended-release capsules), in
the United States, its territories and
Canada, pursuant to the asset purchase
agreement.
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2. To amend Ligands 2002 Stock
Incentive Plan to allow equitable
adjustments to be made to options
outstanding under the plan in the event
of the payment of a large non-recurring
cash dividend.
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3. To approve the adjournment of
the special meeting, if necessary, to
facilitate the approval of proposals 1
or 2, including to permit the
solicitation of additional proxies if
there are not sufficient votes at the
time of the special meeting to
establish a quorum or to approve
proposals 1 or 2.
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4. To transact such other business
as may properly be brought before the
special meeting or any adjournment or
postponement thereof.
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Choose MLinkSM for fast, easy and secure 24/7 online access
to your future proxy materials, investment plan statements,
tax documents and more. Simply log on to Investor
ServiceDirect® at www.melloninvestor.com/isd where
step-by-step instructions will prompt you through enrollment. |
NOTE: Please sign as name appears hereon. Joint owners should each sign. When signing as
attorney, executor, administrator, trustee or guardian, please give full title as such. If signing
for a corporation, give your title. When shares are in the names of more than one person, each
should sign.
5 FOLD AND DETACH HERE 5
Vote by Internet or Telephone or Mail
24 Hours a Day, 7 Days a Week
Internet and telephone voting is available through 11:59 PM Eastern Time
the day prior to Special meeting day.
Your
Internet or telephone vote authorizes the named proxies to vote your shares in the same manner
as if you marked, signed and returned your proxy card.
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Internet |
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http://www.proxyvoting.com/lgnd |
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Use the Internet to vote your
proxy. Have your proxy card in hand
when you access the web site.
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Telephone |
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1-866-540-5760 |
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Use any touch-tone telephone
to vote your proxy. Have your proxy
card in hand when you call.
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Mail |
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Mark, sign and date your proxy card and return it in the enclosed postage-paid envelope.
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If you vote your proxy by Internet or by telephone,
you do NOT need to mail back your proxy card.
You can view the Proxy Statement on the
internet at www.ligand.com on the Investor Relations page
PROXY
THIS PROXY IS SOLICITED ON BEHALF OF THE BOARD OF DIRECTORS OF
LIGAND PHARMACEUTICALS INCORPORATED
The
undersigned hereby appoints Henry F. Blissenbach and Warner R. Broaddus, as proxies, jointly
and severally, with full power of substitution to vote all shares of stock which the undersigned is
entitled to vote at the Special Meeting of Stockholders of Ligand Pharmaceuticals Incorporated to be
held at . local time at the La Jolla Marriott located at 4240 La Jolla Village Drive, La
Jolla, California, 92037 on , 2006, or at any postponements of adjournments
thereof, as specified on the reverse side, and to vote in their discretion on such other business
as may properly come before the Special Meeting and any adjournments thereof.
(Continued and to be marked, dated and signed, on the other side)
Address Change/Comments (Mark the corresponding box on the reverse side)
5 FOLD AND DETACH HERE 5