Delaware
|
|
84-1475642
|
(State
or Other Jurisdiction of Incorporation or Organization)
|
|
(IRS
Employer Identification No.)
|
|
|
|
1180
Avenue of the Americas, 19 th
Floor,
New York, NY
|
|
10036
|
(Address
of Principal Executive Offices)
|
|
(Zip
Code)
|
|
|
|
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Page
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PART
I
|
|
FINANCIAL
INFORMATION
|
|
|
|
|
|
|
|
Item
1.
|
|
Financial
Statements
|
|
|
|
|
|
|
|
|
|
Balance
Sheets September 30, 2006 (unaudited) and December 31,
2005
|
|
3
|
|
|
|
|
|
|
|
Statement
of Operations for the three and nine months ended September 30, 2006
and
2005 (unaudited) and for the period from inception (September 9,
2003) to
September 30, 2006 (unaudited)
|
|
4
|
|
|
|
|
|
|
|
Statement
of Cash Flows for the nine months ended September 30, 2006 and 2005
(unaudited) and for the period from inception (September 9, 2003)
to
September 30, 2006 (unaudited)
|
|
5
|
|
|
|
|
|
|
|
Statement
of Changes in Convertible Preferred Stock and Stockholders’
Equity/(Deficit) for the nine months ended September 30, 2006 (unaudited)
and for the year ended December 31, 2005 and 2004 and for the period
from
inception (September 9, 2003) to December 31, 2003
|
|
6
|
|
|
|
|
|
|
|
Notes
to Unaudited Financial Statements
|
|
7
|
|
|
|
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|
Item
2.
|
|
Management’s
Discussion and Analysis or Plan of Operation
|
|
17
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|
|
|
|
|
Item
3.
|
|
Controls
and Procedures
|
|
24
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|
|
|
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PART
II
|
|
OTHER
INFORMATION
|
|
|
|
|
|
|
|
Item
1.
|
|
Legal
Proceedings
|
|
25
|
|
|
|
|
|
Item
2.
|
|
Unregistered
Sales of Equity Securities and Use of Proceeds
|
|
25
|
|
|
|
|
|
Item
3.
|
|
Defaults
Under Senior Securities
|
|
25
|
|
|
|
|
|
Item
4.
|
|
Submission
of Matters to a Vote of Security Holders
|
|
25
|
|
|
|
|
|
Item
5.
|
|
Other
Information
|
|
26
|
|
|
|
|
|
Item
6.
|
|
Exhibits
|
|
26
|
|
|
Signatures
|
|
27
|
|
|
Exhibit
Index
|
|
28
|
September
30, 2006
|
December
31, 2005
|
||||||
(Unaudited)
|
|||||||
ASSETS
|
|||||||
Current
assets:
|
|||||||
Cash
and cash equivalents
|
$
|
32,962,230
|
$
|
8,880,717
|
|||
Short-term
investments
|
1,536,357
|
—
|
|||||
Prepaid
expenses and other current assets
|
314,785
|
211,837
|
|||||
Total
current assets
|
34,813,372
|
9,092,554
|
|||||
Property
and equipment, net
|
294,982
|
269,702
|
|||||
Deposits
|
9,367
|
5,700
|
|||||
Other
non current assets
|
177,219
|
124,343
|
|||||
Total
assets
|
$
|
35,294,940
|
$
|
9,492,299
|
|||
LIABILITIES
AND STOCKHOLDERS' EQUITY
|
|||||||
Current
liabilities:
|
|||||||
Accounts
payable
|
$
|
1,143,777
|
$
|
835,997
|
|||
Accrued
expenses
|
2,136,961
|
1,418,819
|
|||||
Total
current liabilities
|
3,280,738
|
2,254,816
|
|||||
Deferred
rent
|
39,972
|
35,557
|
|||||
Commitments
and contingencies
|
|||||||
Stockholders'
equity:
|
|||||||
Common
stock, $.001 par value; 280,000,000 shares authorized;
|
|||||||
15,264,248
and 7,247,992 shares issued and outstanding
|
|||||||
at
September 30, 2006 and December 31, 2005, respectively
|
15,264
|
7,248
|
|||||
Additional
paid-in capital
|
59,361,574
|
22,559,034
|
|||||
Deficit
accumulated during the development stage
|
(27,402,608
|
)
|
(15,364,356
|
)
|
|||
Total
stockholders' equity
|
31,974,230
|
7,201,926
|
|||||
Total
liabilities and stockholders' equity
|
$
|
35,294,940
|
$
|
9,492,299
|
|
For
the three
months
ended September 30,
2006
|
For
the three
months
ended September 30,
2005
|
For
the nine
months
ended September 30,
2006
|
For
the nine
months
ended September 30,
2005
|
From
Inception
(Sept.
9, 2003)
through
September
30,
2006
|
|||||||||||
|
|
|
|
|
|
|||||||||||
Research
contract revenue
|
$
|
—
|
$
|
—
|
$
|
—
|
$
|
—
|
$
|
—
|
||||||
|
||||||||||||||||
Operating
expenses and other income:
|
||||||||||||||||
Research
and development
|
2,097,617
|
1,318,608
|
6,545,986
|
4,279,687
|
14,266,443
|
|||||||||||
General
and administrative
|
1,832,361
|
1,541,740
|
6,345,450
|
2,953,830
|
14,281,596
|
|||||||||||
Total
operating expenses
|
3,929,978
|
2,860,348
|
12,891,436
|
7,233,517
|
28,548,039
|
|||||||||||
|
||||||||||||||||
Loss
from operations
|
(3,929,978
|
)
|
(2,860,348
|
)
|
(12,891,436
|
)
|
(7,233,517
|
)
|
(28,548,039
|
)
|
||||||
|
||||||||||||||||
Interest
income
|
475,476
|
94,231
|
853,184
|
177,710
|
1,145,431
|
|||||||||||
Net
loss
|
$
|
(3,454,502
|
)
|
$
|
(2,766,117
|
)
|
$
|
(12,038,252
|
)
|
$
|
(7,055,807
|
)
|
$
|
(27,402,608
|
)
|
|
|
||||||||||||||||
|
||||||||||||||||
Basic
and diluted net loss per share
|
$
|
(0.23
|
)
|
$
|
(0.77
|
)
|
$
|
(1.03
|
)
|
$
|
(2.32
|
)
|
||||
|
||||||||||||||||
Weighted
average common shares
|
||||||||||||||||
outstanding
used to compute basic
|
||||||||||||||||
and
diluted net loss per share share
|
15,264,368
|
3,593,109
|
11,662,722
|
3,041,829
|
|
For
the nine months
ended
September
30, 2006
|
For
the nine months
ended
September
30, 2005
|
For
the Period
from
Inception
(Sept.
9, 2003)
through
September
30, 2006
|
|||||||
Cash
flows from operating activities:
|
||||||||||
Net
loss
|
$
|
(12,038,252
|
)
|
$
|
(7,055,807
|
)
|
$
|
(27,402,608
|
)
|
|
Adjustments
to reconcile net loss to net cash used in operating
activities:
|
||||||||||
Depreciation
and amortization
|
117,155
|
72,519
|
252,340
|
|||||||
Non-cash
stock-based compensation
|
2,530,436
|
—
|
3,332,307
|
|||||||
Gain
on disposal of fixed assets
|
(1,165
|
)
|
—
|
(1,165
|
)
|
|||||
Change
in operating assets and liabilites:
|
||||||||||
(Increase)
decrease in:
|
||||||||||
Prepaid
expenses and other current assets
|
(102,948
|
)
|
(92,245
|
)
|
(314,785
|
)
|
||||
Other
noncurrent assets
|
(52,876
|
)
|
(92,812
|
)
|
(177,219
|
)
|
||||
Deposits
|
(3,667
|
)
|
24,014
|
(9,367
|
)
|
|||||
Increase
(decrease) in:
|
||||||||||
Accounts
payable
|
307,780
|
(232,558
|
)
|
1,143,777
|
||||||
Accrued
expenses
|
718,142
|
391,248
|
2,136,961
|
|||||||
Deferred
rent
|
4,415
|
—
|
39,972
|
|||||||
Net
cash used in operating activities
|
(8,520,980
|
)
|
(6,985,641
|
)
|
(20,999,787
|
)
|
||||
|
||||||||||
Cash
flows from investing activities:
|
||||||||||
Purchases
of property and equipment
|
(141,270
|
)
|
(64,648
|
)
|
(546,157
|
)
|
||||
Increase
in short-term investments
|
(1,536,357
|
)
|
—
|
(1,536,357
|
)
|
|||||
Net
cash used in investing activities
|
(1,677,627
|
)
|
(64,648
|
)
|
(2,082,514
|
)
|
||||
|
||||||||||
Cash
flows from financing activities:
|
||||||||||
Stockholders'
capital contribution
|
—
|
—
|
500,000
|
|||||||
Proceeds
from issuance of common stock and warrants, net
|
34,280,120
|
4,676
|
38,784,935
|
|||||||
Proceeds
from issuance of preferred stock, net
|
—
|
16,759,596
|
16,759,596
|
|||||||
Net
cash provided by financing activities
|
34,280,120
|
16,764,272
|
56,044,531
|
|||||||
|
||||||||||
Net
increase in cash and cash equivalents
|
24,081,513
|
9,713,983
|
32,962,230
|
|||||||
|
||||||||||
Cash
and cash equivalents, beginning of period
|
8,880,717
|
1,026,656
|
—
|
|||||||
|
||||||||||
Cash
and cash equivalents, end of period
|
$
|
32,962,230
|
$
|
10,740,639
|
$
|
32,962,230
|
||||
|
||||||||||
Supplementary
disclosure of cash flow information:
|
||||||||||
Cash
paid for interest
|
$
|
—
|
$
|
—
|
$
|
—
|
||||
|
||||||||||
Cash
paid for income taxes
|
$
|
—
|
$
|
—
|
$
|
—
|
||||
|
||||||||||
Supplementary
disclosure of noncash investing and financing activities:
|
||||||||||
Warrants
issued to placement agents and investors, in connection
with
|
||||||||||
with
private placement
|
$
|
13,092,561
|
$
|
—
|
$
|
13,092,561
|
||||
Warrants
issued to placement agent, in connection
|
||||||||||
with
preferred stock issuance
|
$
|
—
|
$
|
1,682,863
|
$
|
1,682,863
|
||||
Preferred stock conversion to common stock |
$
|
—
|
$
|
16,759,596
|
$
|
16,759,596
|
Convertible
Preferred Stock and Warrants
|
Stockholder's
Equity (Deficit)
|
||||||||||||||||||||||||
Series
A Convertible
Preferred Stock |
Warrants
to Purchase
Series
A Convertible
Preferred
Stock
|
Common
Stock
|
|
|
|||||||||||||||||||||
|
|
Shares
|
|
Amount
|
|
Warrants
|
|
Shares
|
|
Amount
|
|
Additional
Paid- in
Capital |
|
Deficit
Accumulated
During The
Development
Stage
|
Total
Stockholders'
Equity/(Deficit)
|
||||||||||
Stockholders'
contribution,
|
|||||||||||||||||||||||||
September
9, 2003
|
—
|
$
|
—
|
$
|
—
|
250,487
|
$
|
250.00
|
$
|
499,750.00
|
$
|
—
|
$
|
500,000.00
|
|||||||||||
Net
loss
|
—
|
—
|
—
|
—
|
—
|
—
|
(160,136
|
)
|
(160,136
|
)
|
|||||||||||||||
Balance
at December 31, 2003 (audited)
|
0
|
0
|
0
|
250,487
|
250
|
499,750
|
(160,136
|
)
|
339,864
|
||||||||||||||||
Issuance
of common stock
|
—
|
—
|
—
|
2,254,389
|
2,254
|
4,497,746
|
—
|
4,500,000
|
|||||||||||||||||
Issuance
of common stock for services
|
256,749
|
257
|
438,582
|
—
|
438,839
|
||||||||||||||||||||
Fair
value of options/warrants
|
|||||||||||||||||||||||||
issued
for nonemployee services
|
—
|
—
|
—
|
—
|
—
|
264,277
|
—
|
264,277
|
|||||||||||||||||
Net
loss
|
—
|
—
|
—
|
—
|
—
|
—
|
(5,687,297
|
)
|
(5,687,297
|
)
|
|||||||||||||||
Balance
at December 31, 2004 (audited)
|
—
|
—
|
—
|
2,761,625
|
2,761
|
5,700,355
|
(5,847,433
|
)
|
(144,317
|
)
|
|||||||||||||||
Issuance
of Series A convertible preferred
|
|||||||||||||||||||||||||
stock
(net of expenses of $1,340,263 and
|
|||||||||||||||||||||||||
warrant
cost of $1,682,863)
|
4,197,946
|
15,076,733
|
—
|
—
|
—
|
—
|
—
|
—
|
|||||||||||||||||
Fair
value of warrants to purchase Series
|
|||||||||||||||||||||||||
A
convertible preferred stock
|
—
|
—
|
1,682,863
|
—
|
—
|
—
|
—
|
—
|
|||||||||||||||||
Issuance
of Common stock to EasyWeb
|
|||||||||||||||||||||||||
Shareholders
|
—
|
—
|
—
|
189,922
|
190
|
(190
|
)
|
—
|
—
|
||||||||||||||||
Conversion
of Series A convertible
|
|||||||||||||||||||||||||
preferred
stock @ $0.001 into $0.001
|
|||||||||||||||||||||||||
common
stock on September 13, 2005
|
|||||||||||||||||||||||||
at
an exchange ratio of .500974
|
(4,197,946
|
)
|
(15,076,733
|
)
|
(1,682,863
|
)
|
4,197,823
|
4,198
|
16,755,398
|
—
|
16,759,596
|
||||||||||||||
Issuance
of common stock for options
|
—
|
—
|
—
|
98,622
|
99
|
4,716
|
—
|
4,815
|
|||||||||||||||||
Fair
value of options/warrants issued for
|
|||||||||||||||||||||||||
nonemployee
services
|
—
|
—
|
—
|
—
|
—
|
98,755
|
—
|
98,755
|
|||||||||||||||||
Net
loss
|
—
|
—
|
—
|
—
|
—
|
—
|
(9,516,923
|
)
|
(9,516,923
|
)
|
|||||||||||||||
Balance
at December 31, 2005 (audited)
|
—
|
—
|
—
|
7,247,992
|
7,248
|
22,559,034
|
(15,364,356
|
)
|
7,201,926
|
||||||||||||||||
Issuance
of common stock in private
|
|||||||||||||||||||||||||
placement,
net of expenses $2,719,395
|
—
|
—
|
—
|
7,991,256
|
7,991
|
21,179,568
|
—
|
21,187,559
|
|||||||||||||||||
Issuance
of warrants
|
—
|
—
|
—
|
—
|
—
|
13,092,561
|
—
|
13,092,561
|
|||||||||||||||||
Issuance
of common stock for
|
|||||||||||||||||||||||||
services
rendered
|
—
|
—
|
—
|
25,000
|
25
|
106,225
|
—
|
106,250
|
|||||||||||||||||
Stock
based compensation for
|
|||||||||||||||||||||||||
employees
|
—
|
—
|
—
|
—
|
—
|
2,424,186
|
—
|
2,424,186
|
|||||||||||||||||
Net
loss
|
—
|
—
|
—
|
—
|
—
|
—
|
(12,038,252
|
)
|
(12,038,252
|
)
|
|||||||||||||||
Balance
at September 30, 2006 (unaudited)
|
—
|
$
|
—
|
$
|
—
|
15,264,248
|
$
|
15,264
|
$
|
59,361,574
|
$
|
(27,402,608
|
)
|
$
|
31,974,230
|
1.
|
BASIS
OF PRESENTATION AND
OPERATIONS
|
2.
|
STOCK
BASED COMPENSATION
|
|
|
Three
months ended
September 30, 2006 |
|
Nine
months ended
September 30, 2006 |
|||
Research
and development, including costs of research contracts
|
$
|
101,928
|
$
|
266,174
|
|||
General
and administrative
|
228,535
|
2,158,012
|
|||||
Share
based compensation expense before tax
|
330,463
|
2,424,186
|
|||||
Income
tax benefit
|
—
|
—
|
|||||
Net
compensation expense
|
$
|
330,463
|
$
|
2,424,186
|
|
|
Three
months ended
September 30, 2005 |
|
Nine
months ended
September 30, 2005 |
|||
Net
loss:
|
$
|
(2,766,117
|
)
|
$
|
(7,055,807
|
)
|
|
As
reported
|
|||||||
Stock-based
compensation expense included in reported net loss
|
—
|
—
|
|||||
Stock-based
compensation expense under the fair value-based method
|
(176,297
|
)
|
(340,197
|
)
|
|||
Pro
forma net loss
|
$
|
(2,942,414
|
)
|
$
|
(7,396,004
|
)
|
|
Basic
and diluted net loss per share:
|
|||||||
As
reported
|
$
|
(0.77
|
)
|
$
|
(2.32
|
)
|
|
Pro
forma
|
$
|
(0.82
|
)
|
$
|
(2.43
|
)
|
3.
|
CONVERTIBLE
PREFERRED STOCK AND STOCKHOLDERS’
EQUITY
|
4.
|
RELATED
PARTY TRANSACTIONS
|
5.
|
STOCK
OPTION PLAN
|
|
Number
of Shares
|
Weighted
Average Exercise
Price |
Weighted
Average
Remaining
Contractual
Term
(Years)
|
Aggregate Intrinsic
Value |
|||||||||
Outstanding,
January 1, 2006
|
973,639
|
$ |
2.56
|
||||||||||
Granted
|
705,930
|
5.02
|
|||||||||||
Exercised
|
—
|
—
|
|||||||||||
Canceled
|
22,939
|
4.19
|
|||||||||||
Outstanding,
September 30, 2006
|
1,656,630
|
$ |
3.56
|
8.76
|
$ |
2,679,983
|
|||||||
Options
exercisable, September 30, 2006
|
942,097
|
$ |
3.43
|
8.68
|
$ |
1,622,360
|
6.
|
WARRANTS
|
|
·
|
ZIO-101
is an organic arsenic compound covered by issued U.S. patents and
applications internationally. A form of commercially available inorganic
arsenic (arsenic trioxide (Trisenox®) or ATO) has been approved for the
treatment of acute promyelocytic leukemia (APL), a precancerous condition,
and is on the compendia listing for the therapy of multiple myeloma
as
well as having been studied for the treatment of various other cancers.
Nevertheless, ATO has been shown to be toxic to the heart, liver,
and
brain, limiting its use as an anti-cancer agent. Inorganic arsenic
has
also been shown to cause cancer of the skin and lung in humans. The
toxicity of arsenic generally is correlated to its accumulation in
organs
and tissues. Our preclinical and phase I clinical studies to date
have
demonstrated that ZIO-101 (and organic arsenic in general) is considerably
less toxic than inorganic arsenic, particularly with regard to heart
toxicity. In vitro testing of ZIO-101 using the National Cancer
Institute’s human cancer cell panel detected activity against lung, colon,
brain, melanoma, ovarian and kidney cancer. Moderate activity was
detected
against breast and prostate cancer. In addition to solid tumors,
in vitro
testing in both the National Cancer Institute’s cancer cell panel and in
vivo testing in a leukemia animal model demonstrated substantial
activity
against hematological cancers (cancers of the blood and blood-forming
tissues) such as leukemia, lymphoma, myelodysplastic syndromes and
multiple myeloma.
|
|
|
Phase
I testing of the intravenous (IV) form of ZIO-101 is ongoing with
two
safety and dose finding studies. The Company has seen encouraging
signs of
clinical activity in both of these studies.. The Company has progressed
an
ongoing phase I/II study in advanced multiple myeloma designed to
determine maximum tolerated dose and to assess clinical activity
in this
specific indication. The Company expects to pursue registration in
the
U.S. for the treatment of advanced multiple myeloma with a potentially
pivotal trial to begin in late 2007. The Company also expects to
initiate
additional phase II studies in other hematological and solid tumor
cancers
while also exploring different dosing schedules and to file a U.S.
Investigational New Drug Application for the clinical study of an
oral
form of ZIO-101.
|
|
·
|
ZIO-201,
or isophosphoramide mustard (IPM), is a proprietary stabilized metabolite
of ifosfamide that is also related to cyclophosphamide. A patent
application for pharmaceutical composition has been filed.
Cyclophosphamide and ifosfamide are alkylating agents. The Company
believes cyclophosphamide is the most widely used alkylating agent
in
cancer therapy and is used to treat breast cancer and non-Hodgkin’s
lymphoma. Ifosfamide has been shown to be effective in high dose
by
itself, or in combination in treating sarcoma and lymphoma. Although
ifosfamide-based treatment generally represents the standard of care
for
sarcoma, it is not licensed for this indication by the Food and Drug
Administration. Our preclinical studies have shown that, in animal
and
laboratory models, IPM evidences activity against leukemia and solid
tumors. These studies also indicate that ZIO-201 has a better
pharmacokinetic and safety profile than ifosfamide or cyclophosphamide,
offering the possibility of safer and more efficacious therapy with
ZIO-201. Ifosfamide is metabolized to IPM. In addition to IPM, another
metabolite of ifosfamide is acrolein, which is toxic to the kidneys
and
bladder. The presence of acrolein can mandate the administration
of a
protective agent called mesna, which is inconvenient and expensive.
Chloroacetaldehyde is another metabolite of ifosfamide and is toxic
to the
central nervous system, causing “fuzzy brain” syndrome for which there is
currently no protective measure. Similar toxicity concerns pertain
to
high-dose cyclophosphamide, which is widely used in bone marrow and
blood
cell transplantation. Because ZIO-201 is independently active without
acrolein or chloroacetaldehyde metabolites, the Company believes
that the
administration of ZIO-201 may avoid many of the toxicities of ifosfamide
and cyclophosphamide without compromising efficacy. In addition to
anticipated lower toxicity, ZIO-201 (and without the co-administration
of
mesna) may have other advantages over ifosfamide. In preclinical
studies
ZIO-201 likely cross-links DNA differently than ifosfamide or
cyclophosphamide metabolites, resulting in a different activity profile.
Moreover, in some instances ZIO-201 appears to show activity in
ifosfamide- and/or cyclophosphamide-resistant cancer
cells.
|
|
|
|
|
|
Phase
I testing of the IV form of ZIO-201 is ongoing at two sites in the
U.S.
IPM has been administered without the “uroprotectant” mesna and the
toxicities associated with acrolein and chloroacetaldehyde have not
been
observed. Electrolyte inbalances seen with ifosfamide have occurred
in the
higher dose cohorts. The Company has seen encouraging signs of clinical
activity in the phase I study. The Company initiated a phase I/II
trial in
advanced sarcoma designed to determine maximum tolerated dose and
to
assess clinical activity in this specific indication. The Company
expects
to pursue registration in the U.S. for the treatment of advanced
sarcoma
with a potentialy pivotal trial to begin in late 2007. The Company
also
expects to initiate additional phase II studies in other cancers
and using
different dosing schedules and routes of administration and to file
a U.S.
Investigational New Drug Application for an oral form of
ZIO-201.
|
·
|
Fees
and milestone payments required under the license agreements relating
to
our existing product candidates and additional in-licensed
candidates;
|
·
|
Clinical
trial expenses, including the costs incurred with respect to the
conduct
of clinical trials for ZIO-101 and ZIO-201, ZIO-301, and preclinical
costs
associated with back-up candidates ZIO-102 and ZIO-202;
|
·
|
Costs
related to the scale-up and manufacture of ZIO-101, ZIO-201, and
ZIO-301;
|
·
|
Rent
for our facilities; and
|
·
|
General
corporate and working capital, including general and administrative
expenses.
|
·
|
Changes
in the focus and direction of our research and development programs,
including the acquisition and pursuit of development of new product
candidates;
|
·
|
Competitive
and technical advances;
|
·
|
Costs
of commercializing any of the product candidates;
|
·
|
Costs
of filing, prosecuting, defending and enforcing any patent claims
and any
other intellectual property rights;
|
|
or
other developments.
|
Payments
due by Period
|
||||||||||||||||
Total
|
|
Less
than 1 Year
|
|
1
- 3 Years
|
|
4
- 5 Years
|
|
After
5 Years
|
||||||||
Operating
lease
|
$
|
855,343
|
$
|
275,091
|
$
|
504,220
|
$
|
76,032
|
-
|
Exhibit
No.
|
|
Description
|
|
|
|
10.1
|
Asset Purchase Agreement dated November 3, 2006 by and among Baxter Healthcare S.A., Baxter International, Inc., Baxter Oncology GmbH and ZIOPHARM Oncology, Inc.† | |
10.2
|
License Agreement dated November 3, 2006 by and among Baxter Healthcare S.A., Baxter International, Inc. and ZIOPHARM Oncology, Inc.† | |
31.1
|
|
Certification
of Chief Executive Officer
|
31.2
|
|
Certification
of Chief Financial Officer
|
32.1
|
|
Certifications
of Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
|
32.2
|
|
Certifications
of Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
|
99.1
|
Press Release dated November 13, 2006. |
|
|
|
|
ZIOPHARM
ONCOLOGY, INC.
|
|
|
|
|
Date: November
13, 2006
|
By:
|
/s/ Jonathan
Lewis
|
|
Jonathan
Lewis
Chief
Executive Officer
(Principal
Executive Officer)
|
|
|
|
|
|
|
|
|
|
|
|
|
Date: November
13, 2006
|
By:
|
/s/ Richard
Bagley
|
|
Richard
Bagley
Chief
Financial Officer
(Principal
Financial and Accounting Officer)
|
|
|
|
Exhibit
No.
|
|
Description
|
|
|
|
10.1
|
Asset Purchase Agreement dated November 3, 2006 by and among Baxter Healthcare S.A., Baxter International, Inc., Baxter Oncology GmbH and ZIOPHARM Oncology, Inc.† | |
10.2
|
License Agreement dated November 3, 2006 by and among Baxter Healthcare S.A., Baxter International, Inc. and ZIOPHARM Oncology, Inc.† | |
31.1
|
|
Certification
of Chief Executive Officer
|
31.2
|
|
Certification
of Chief Financial Officer
|
32.1
|
|
Certifications
of Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
|
32.2
|
|
Certifications
of Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
|
99.1
|
Press Release dated November 13, 2006. |