UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported)
March 3, 2010
WATSON PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Its Charter)
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Nevada
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001-03305
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95-3872914 |
(State or Other Jurisdiction
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(Commission File Number)
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(IRS Employer |
of Incorporation)
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Identification No.) |
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311 Bonnie Circle |
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Corona, California
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92880 |
(Address of Principal Executive Offices)
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(Zip Code) |
Registrants telephone number, including area code: (951) 493-5300
(Former name or former address, if changed since last report): Not applicable.
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy
the filing obligation of the registrant under any of the following provisions:
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
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Pre-commencement communications pursuant to Rule 14d-2(b)
under the Exchange Act (17 CFR 240.14d-2(b)) |
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Pre-commencement communications pursuant to Rule 13e-4(c)
under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 1.01. Entry into a Material Definitive Agreement.
On March 3, 2010, Watson Pharmaceuticals, Inc. (Watson) and Coventry Acquisition,
Inc. (Purchaser), a Delaware corporation and wholly-owned subsidiary of Watson, entered
into a Purchase and Collaboration Agreement (the Purchase Agreement) with Columbia
Laboratories, Inc., a Delaware corporation (Columbia), pursuant to which Purchaser agreed
to purchase from Columbia (i) substantially all of Columbias assets primarily relating to
pharmaceutical products containing progesterone as an active ingredient, including CRINONE 8%
progesterone gel, PROCHIEVE 8% progesterone gel and PROCHIEVE 4% progesterone gel, each sold by
Columbia in the United States (together, the Progesterone Products), including certain
intellectual property, promotional materials, contracts, product data and regulatory approvals and
regulatory filings (together, the Purchased Assets), and (ii) 11,200,000 newly issued
restricted shares of the Columbias common stock, $.01 par value per share (the Shares).
Columbia will retain certain progesterone related assets and rights, including all rights necessary
to perform its obligations under its agreement with an affiliate of Merck Serono S.A.
Pursuant to the terms of the Purchase Agreement, at the closing, in exchange for the
Shares and the Purchased Assets, Purchaser will assume certain liabilities and pay to Columbia
$47.0 million in cash and Columbia will receive the right to receive up to $45.5 million in future
payments, contingent on the achievement of certain milestones, including clinical trial results,
regulatory approvals and product launches as described in the Purchase Agreement. Purchaser has
also agreed to pay to Columbia a percentage of the net sales of and/or gross profits relating to
certain Progesterone Products and any next generation products, as described in the Purchase
Agreement. Pursuant to the Purchase Agreement, Columbia and Purchaser have also agreed to
collaborate with respect to the development of Progesterone Products. In connection therewith, the
parties agreed to establish a joint development committee to oversee and supervise all development
activities. Columbia will be responsible for completion of the PREGNANT Study (as defined in the
Purchase Agreement) and such other activities as determined by the joint development committee.
Columbia will be responsible for the costs of conducting the PREGNANT Study and the preparation,
filing and approval process of the related new drug application (or supplemental new drug
application) up to a maximum amount of $7.0 million from January 1, 2010. All other development
costs incurred in connection with the development and collaboration will be paid by Purchaser.
Purchaser and Columbia have each made customary representations, warranties and covenants in
the Purchase Agreement. These include, among other things, Columbias agreement to operate its
business in the ordinary course until closing, not to compete with Watson in the progesterone
business for a limited time after closing (subject to certain exceptions), not to solicit any
Acquisition Proposal (as defined in the Purchase Agreement) and customary indemnification
obligations. Watson has agreed to guarantee the obligations of Purchaser under the Purchase
Agreement.
The closing of the transaction is subject to receiving approval from the stockholders of
Columbia and other customary conditions. If the Purchase Agreement is terminated under certain
circumstances as described in the Purchase Agreement, Columbia will be required to pay Purchaser a
termination fee of $2.0 million.
Purchaser and Columbia have agreed to enter into related ancillary transaction agreements at
the closing of the transaction, including a license agreement relating to the grant of certain
intellectual property licenses, a supply agreement and an investors rights agreement. Under the
supply agreement, Columbia will supply PROCHIEVE 4%, PROCHIEVE 8% and CRINONE 8% to the Buyer for
sale in the United States at a price equal to 110% of the cost of goods sold. Under the investors
rights agreement, Columbia will grant Purchaser certain registration rights with respect to the
resale of the Shares and the right to designate one member to Columbias board of directors until
Purchaser no longer owns at least 10% of Columbias outstanding common stock and Purchaser will
agree to certain limitations relating to the Shares.
The foregoing description of the Purchase Agreement does not purport to be complete and is
qualified in its entirety by reference to the full text of the Purchase Agreement (attached hereto
as Exhibit 2.1 and incorporated herein by reference).