As
filed with the Securities and Exchange Commission on May 10,
2010
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Registration
No. 333-166444
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Delaware
(State
or jurisdiction
of
incorporation or organization)
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84-1475642
(I.R.S.
Employer
Identification
No.)
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Dr.
Jonathan Lewis
Chief
Executive Officer
ZIOPHARM
Oncology, Inc.
1180
Avenue of the Americas, 19th Floor
New
York, NY 10036
Telephone:
(646) 214-0700
Facsimile:
(646) 214-0711
(Name,
address and telephone number of agent for service)
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Copies
to:
Alan
M. Gilbert, Esq.
Maslon
Edelman Borman & Brand, LLP
90
South 7th Street, Suite 3300
Minneapolis,
Minnesota 55402
Telephone:
(612) 672-8200
Facsimile:
(612) 642-8381
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Large
accelerated filer ¨
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Accelerated
filer ¨
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Non-accelerated
filer ¨
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Smaller
reporting company þ
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(Do
not check if a smaller reporting company)
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Title Of Each Class Of
Securities To Be Registered
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Amount To Be
Registered (1)
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Proposed Maximum
Offering Price
Per Share (1) (2)
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Proposed Maximum
Aggregate
Offering Price (1) (2)
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Amount Of
Registration Fee (3)
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||||||||||||
Common
stock, par value $0.001 per share
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(4 | ) | (4 | ) | (4 | ) | (4 | ) | ||||||||
Preferred
Stock, par value $0.001 per share
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(4 | ) | (4 | ) | (4 | ) | (4 | ) | ||||||||
Warrants
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(4 | ) | (4 | ) | (4 | ) | (4 | ) | ||||||||
Debt
Securities
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(4 | ) | (4 | ) | (4 | ) | (4 | ) | ||||||||
Total
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(4 | ) | (4 | ) | $ | 100,000,000 | $ | 7,130 | (5) |
(1)
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An
indeterminate number of shares of common stock and preferred stock, an
indeterminate number of warrants to purchase debt securities, common stock
or preferred stock and an indeterminate amount of debt securities are
being registered hereunder, but in no event will the aggregate initial
offering price exceed $100,000,000. If any debt securities are issued at
an original issue discount, then the offering price of such debt
securities shall be in such greater principal amount as shall result in an
aggregate initial offering price not to exceed $100,000,000, less the
aggregate dollar amount of all securities previously issued hereunder. Any
securities registered hereunder may be sold separately or as units with
other securities registered hereunder. The securities registered also
include such indeterminate amount and number of shares of common stock and
preferred stock as may be issued upon conversion of or exchange for
preferred stock and provide for conversion or exchange, upon exercise of
warrants or pursuant to antidilution provisions of any such securities. In
addition, pursuant to Rule 416 under the Securities Act, there are also
being registered hereunder an indeterminate number of shares of common
stock and preferred stock as may be issuable with respect to the shares
being registered hereunder as a result of stock splits, stock dividends or
similar transactions.
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(2)
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Unspecified
pursuant to General Instruction II.D to Form S-3 under the Securities
Act.
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(3)
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Calculated
pursuant to Rule 457(o) under the Securities
Act.
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(4)
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Not
required to be included in accordance with General Instruction II.D. of
Form S-3.
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(5)
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Previously
paid upon the registrant’s initial filing on April 30,
2010.
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Page
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About
This Prospectus
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i
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Prospectus
Summary
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1
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Risk
Factors
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4
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Special
Note Regarding Forward-Looking Statements
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4
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Ratio
of Earnings to Fixed Charges
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5
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Use
of Proceeds
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5
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Plan
of Distribution
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5
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Description
of Capital Stock
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6
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Description
of Debt Securities
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8
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Description
of Warrants
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16
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Certain
Provisions of Delaware Law, the Certificate of Incorporation and
Bylaws
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18
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Where
You Can Find More Information
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20
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Incorporation
of Certain Information by Reference
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20
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Legal
Matters
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21
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Experts
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21
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·
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ZIO-101
or darinaparsin (ZinaparTM)
is an anti-mitochondrial (organic arsenic) compound covered by issued
patents and pending patent applications in the U.S. and in foreign
countries. A form of commercially available inorganic arsenic (arsenic
trioxide [Trisenox ®] or “ATO”) has been approved in the United States and
the European Union and Japan for the treatment of acute promyelocytic
leukemia, a precancerous condition. In the United States, ATO is on the
compendia listing for the therapy of multiple myeloma, and has been
studied for the treatment of various other cancers. Nevertheless, ATO has
been shown to be toxic to the heart, liver, and brain, which limits its
use as an anti-cancer agent. ATO carries a “black box” warning for ECG
abnormalities since arsenic trioxide has been shown to cause QT interval
prolongation and complete atrioventricular block. QT prolongation can lead
to a torsade de pointes-type ventricular arrhythmia, which can be fatal.
Inorganic arsenic has also been shown to cause cancer of the skin and lung
in humans. The toxicity of arsenic is generally correlated to its
accumulation in organs and tissues. Our preclinical and clinical studies
to date have demonstrated that darinaparsin is considerably less toxic
than ATO, particularly with regard to cardiac toxicity. In vitro testing
of darinaparsin using the National Cancer Institute’s human cancer cell
panel demonstrated activity against a series of tumor cell lines including
lung, colon, brain, melanoma, ovarian, and kidney cancer. Moderate
activity was shown against breast and prostate cancer tumor cell lines. 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. Results
indicate significant activity against the HuT 78 cutaneous T-cell
lymphoma, the NK-G2MI natural killer-cell NHL, KARPAS-299 T-cell NHL,
SU-DHL-8 B-cell NHL, SU-DHL-10 B-cell NHL and SU-DHL-16 B-cell NHL cell
lines. Preclinical studies have also established anti-angiogenic
properties of darinaparsin and provided support for the development of an
oral capsule form of the drug, and established synergy of darinaparsin in
combination with other approved anti-cancer
agents.
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Phase
I testing of the intravenous (IV) form of darinaparsin in solid tumors and
hematological cancers has been completed. We reported clinical activity
and, importantly, a safety profile from these studies as predicted by
preclinical results. We subsequently completed Phase II studies in
advanced myeloma and primary liver cancer and are nearing completion of a
Phase II study in certain other hematological cancers. In addition, we are
completing two Phase I studies with an oral capsule form of darinaparsin.
At the May 2009 annual meeting of the American Society of Clinical
Oncology, we reported favorable results from the trial with
IV-administered darinaparsin in lymphoma, particularly peripheral T-cell
lymphoma. In the ongoing Phase I trials, also reported at the ASCO annual
meeting, preliminary data primarily in solid tumors indicate the oral form
is active and well tolerated. We are completing data collection from the
IV Phase II trial to address a registration and other trials with the U.S.
Food and Drug Administration. The oral Phase I program will be progressed
to establish a dose for further clinical
testing.
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·
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ZIO-201
or palifosfamide (ZymafosTM
), comprises the active metabolite of ifosfamide, a compound chemically
related to cyclophosphamide. Patent applications covering proprietary
forms of palifosfamide for pharmaceutical composition and method of use
have been filed in the U.S. and internationally and in the U.S. we
recently received a patent covering pharmaceutical composition. Like
cyclophosphamide, ifosfamide and bendamustine, palifosfamide is a DNA
alkylating agent, a form of cancer therapy to treat a wide range of solid
tumors and hematological malignancies. We believe that cyclophosphamide is
the most widely used alkylating agent in cancer therapy, with significant
use in the treatment of breast cancer and non-Hodgkin’s lymphoma.
Bendamustine has been recently approved and successfully launched by
Cephalon Oncology in the U.S. and Europe to treat certain hematological
malignancies. Ifosfamide has been shown to be effective in the treatment
of sarcoma and lymphoma, either by itself or in combination with other
anticancer agents. Ifosfamide is approved by the FDA as a treatment for
testicular cancer while ifosfamide-based treatment is a standard of care
for sarcoma, although it is not licensed for this indication by the FDA.
Preclinical studies have shown that palifosfamide has activity against
leukemia and solid tumors. These studies also indicate that palifosfamide
may have a better safety profile than ifosfamide or cyclophosphamide
because it does not appear to produce known toxic metabolites of
ifosfamide, such as acrolein and chloroacetaldehyde. Acrolein, which is
toxic to the kidneys and bladder, can mandate the administration of a
protective agent called mesna, which is inconvenient and expensive.
Chloroacetaldehyde 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. Palifosfamide
has evidenced activity against ifosfamide- and/or
cyclophosphamide-resistant cancer cell lines. Also in preclinical cancer
models, palifosfamide was shown to be orally active and encouraging
results have been obtained with palifosfamide in combination with
doxorubicin, an agent approved to treat
sarcoma.
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·
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ZIO-301
or indibulin (ZybulinTM
), is a novel, orally available small molecular-weight inhibitor of
tubulin polymerization that we acquired from Baxter Healthcare in 2006 and
is the subject of numerous patents worldwide, including the United States,
the European Union and Japan. The microtubule component, tubulin, is one
of the more well established drug targets in cancer. Microtubule
inhibitors interfere with the dynamics of tubulin polymerization,
resulting in inhibition of chromosome segregation during mitosis and
consequently inhibition of cell division. A number of marketed IV
anticancer drugs target tubulin, such as the taxane family members,
paclitaxel (Taxol ® ), docetaxel (Taxotere ® ) , the Vinca alkaloid family
members, vincristine and vinorelbine, and the new class of epothilones
with IxempraTM
marketed. This class of agents is typically the mainstay of therapy in a
wide variety of indications. In spite of their effectiveness, the use of
these drugs is associated with significant toxicities, notably peripheral
neurotoxicity.
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·
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the
progress and timing of preclinical and clinical trials involving our drug
candidates;
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·
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the
progress and timing of our research and development
programs;
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·
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the
benefits to be derived from relationships with our
collaborators;
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·
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the
receipt or anticipated receipt of regulatory clearances and
approvals;
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·
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our
ability to enforce intellectual property
rights;
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·
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our
estimates of future revenues and profitability;
and
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·
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our
estimates regarding our capital requirements and our need for additional
financing.
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Fiscal Year Ended December 31,
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Three Months
Ended
March 31,
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|||||||||||||||||||||||
$ In Thousands, Except Ratio
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2005
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2006
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2007
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2008
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2009
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2010
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||||||||||||||||||
Ratio
of earnings to fixed charges(1)
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- | - | - | - | - | - | ||||||||||||||||||
Deficiency
of earnings to fixed charges(2)
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$ | (9,517 | ) | $ | (17,857 | ) | $ | (26,608 | ) | $ | (25,231 | ) | $ | (7,649 | ) | $ | (17,653 | ) |
(1)
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In
each of the periods presented, no earnings were sufficient to cover fixed
charges.
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(2)
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The
deficiency of earnings is equivalent to net income (loss) before tax
benefit (provision) and extraordinary
gain.
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·
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to
or through one or more underwriters or
dealers;
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·
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directly
to purchasers, or to purchasers through agents;
or
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·
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through
a combination of any of these methods of
sale.
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·
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from
time to time in one or more transactions at a fixed price or prices, which
may be changed from time to time;
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·
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at
market prices prevailing at the times of
sale;
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·
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at
prices related to such prevailing market prices;
or
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·
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at
negotiated prices.
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·
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the
number of shares constituting that
series;
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·
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dividend
rights and rates;
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·
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voting
rights;
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·
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conversion
terms;
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·
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rights
and terms of redemption (including sinking fund provisions);
and
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·
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rights
of the series in the event of liquidation, dissolution or winding
up.
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·
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the
title and stated value of the preferred
stock;
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·
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the
number of shares of the preferred stock offered, the liquidation
preference per share and the offering price of the preferred
stock;
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·
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the
dividend rate(s), period(s) and/or payment date(s) or method(s) of
calculation applicable to the preferred
stock;
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·
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whether
dividends are cumulative or non-cumulative and, if cumulative, the date
from which dividends on the preferred stock will
accumulate;
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·
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the
procedures for any auction and remarketing, if any, for the preferred
stock;
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·
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the
provisions for a sinking fund, if any, for the preferred
stock;
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·
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the
provision for redemption, if applicable, of the preferred
stock;
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·
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any
listing of the preferred stock on any securities
exchange;
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·
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the
terms and conditions, if applicable, upon which the preferred stock will
be convertible into common stock, including the conversion price (or
manner of calculation) and conversion
period;
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·
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voting
rights, if any, of the preferred
stock;
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·
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a
discussion of any material and/or special United States federal income tax
considerations applicable to the preferred
stock;
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·
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the
relative ranking and preferences of the preferred stock as to dividend
rights and rights upon the liquidation, dissolution or winding up of our
affairs;
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·
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any
limitations on issuance of any class or series of preferred stock ranking
senior to or on a parity with the class or series of preferred stock as to
dividend rights and rights upon liquidation, dissolution or winding up of
our affairs; and
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·
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any
other specific terms, preferences, rights, limitations or restrictions of
the preferred stock.
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·
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the offering
price;
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·
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the
title;
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·
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any limit on the aggregate
principal amount;
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·
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the person who shall be entitled
to receive interest, if other than the record holder on the record
date;
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·
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the date the principal will be
payable;
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·
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the interest rate, if any, the
date interest will accrue, the interest payment dates and the regular
record dates;
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·
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the place where payments may be
made;
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·
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any mandatory or optional
redemption provisions;
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·
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if applicable, the method for
determining how the principal, premium, if any, or interest will be
calculated by reference to an index or
formula;
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·
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if other than U.S. currency, the
currency or currency units in which principal, premium, if any, or
interest will be payable and whether we or the holder may elect payment to
be made in a different
currency;
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·
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the portion of the principal
amount that will be payable upon acceleration of stated maturity, if other
than the entire principal
amount;
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·
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any defeasance provisions if
different from those described below under “Satisfaction and Discharge;
Defeasance”;
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·
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any conversion or exchange
provisions;
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·
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any obligation to redeem or
purchase the debt securities pursuant to a sinking
fund;
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·
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whether the debt securities will
be issuable in the form of a global
security;
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·
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any subordination provisions, if
different from those described below under
“Subordination”;
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·
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any deletions of, or changes or
additions to, the events of default or covenants;
and
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·
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any other specific terms of such
debt securities.
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·
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issue, register the transfer of,
or exchange, any debt security of that series during a period beginning at
the opening of business 15 days before the day of mailing of a notice of
redemption and ending at the close of business on the day of the mailing;
or
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·
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register the transfer of or
exchange any debt security of that series selected for redemption, in
whole or in part, except the unredeemed portion being redeemed in
part.
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·
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be registered in the name of a
depositary that we will identify in a prospectus
supplement;
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·
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be deposited with the depositary
or nominee or custodian; and
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·
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bear any required
legends.
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·
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the depositary has notified us
that it is unwilling or unable to continue as depositary or has ceased to
be qualified to act as
depositary;
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an event of default is
continuing; or
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·
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the Company executes and delivers
to the trustee an officers’ certificate stating that the global security
is exchangeable.
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will not be entitled to have the
debt securities registered in their
names;
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will not be entitled to physical
delivery of certificated debt securities;
and
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·
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will not be considered to be
holders of those debt securities under the
indentures.
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the successor, if any, is a U.S.
corporation, limited liability company, partnership, trust or other
entity;
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·
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the successor assumes our
obligations on the debt securities and under the
indenture;
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·
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immediately after giving effect
to the transaction, no default or event of default shall have occurred and
be continuing; and
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·
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certain other conditions are
met.
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(1)
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failure
to pay principal of or any premium on any debt security of that series
when due;
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(2)
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failure
to pay any interest on any debt security of that series for 30 days when
due;
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(3)
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failure
to deposit any sinking fund payment when
due;
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(4)
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failure
to perform any other covenant in the indenture continued for 90 days after
being given the notice required in the
indenture;
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(5)
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our
bankruptcy, insolvency or reorganization;
and
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(6)
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any
other event of default specified in the prospectus
supplement.
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(1)
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the holder has previously given
to the trustee written notice of a continuing event of default with
respect to the debt securities of that
series;
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(2)
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the holders of at least 25% in
aggregate principal amount of the outstanding debt securities of that
series have made a written request and have offered reasonable indemnity
to the trustee to institute the proceeding;
and
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(3)
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the trustee has failed to
institute the proceeding and has not received direction inconsistent with
the original request from the holders of a majority in aggregate principal
amount of the outstanding debt securities of that series within 90 days
after the original request.
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·
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change
the amount of securities whose holders must consent to an amendment,
supplement or waiver;
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·
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change the stated maturity of any
debt security;
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·
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reduce the principal on any debt
security or reduce the amount of, or postpone the date fixed for, the
payment of any sinking fund;
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·
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reduce the principal of an
original issue discount security on acceleration of
maturity;
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·
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reduce the rate of interest or
extend the time for payment of interest on any debt
security;
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·
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make a principal or interest
payment on any debt security in any currency other than that stated in the
debt security;
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·
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impair the right to enforce any
payment after the stated maturity or redemption
date;
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·
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waive any default or event of
default in payment of the principal of, premium or interest on any debt
security (except certain rescissions of acceleration);
or
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·
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waive a redemption payment or
modify any of the redemption provisions of any debt
security.
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·
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to provide for the issuance of
and establish the form and terms and conditions of debt securities of any
series as permitted by the
indenture;
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·
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to provide for uncertificated
securities in addition to or in place of certificated
securities;
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·
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to provide for the assumption of
our obligations to holders of any debt security in the case of a merger,
consolidation, transfer or sale of all or substantially all of our
assets;
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·
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to make any change that does not
adversely affect the legal rights under the indenture of any such
holder;
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·
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to comply with requirements of
the Commission in order to effect or maintain the qualification of an
indenture under the Trust Indenture Act;
or
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·
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to evidence and provide for the
acceptance of appointment by a successor trustee with respect to the debt
securities of one or more series and to add to or change any of the
provisions of the indenture as shall be necessary to provide for or
facilitate the administration of the trusts by more than one
Trustee.
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·
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to be discharged from all of our
obligations, subject to limited exceptions, with respect to any series of
debt securities then outstanding;
and/or
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·
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to be released from our
obligations under the following covenants and from the consequences of an
event of default resulting from a breach of certain covenants, including
covenants as to payment of taxes and maintenance of corporate
existence.
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·
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a default in the payment of the
principal, premium, if any, interest, rent or other obligations in respect
of designated senior indebtedness occurs and is continuing beyond any
applicable period of grace (called a “payment default”);
or
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·
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a default other than a payment
default on any designated senior indebtedness occurs and is continuing
that permits holders of designated senior indebtedness to accelerate its
maturity, and the trustee receives notice of such default (called a
“payment blockage notice) from us or any other person permitted to give
such notice under the indenture (called a “non-payment
default”).
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(1)
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all
indebtedness, obligations and other liabilities for borrowed money,
including overdrafts, foreign exchange contracts, currency exchange
agreements, interest rate protection agreements, and any loans or advances
from banks, or evidenced by bonds, debentures, notes or similar
instruments, other than any account payable or other accrued current
liability or obligation incurred in the ordinary course of business in
connection with the obtaining of materials or
services;
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(2)
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all
reimbursement obligations and other liabilities with respect to letters of
credit, bank guarantees or bankers’
acceptances;
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(3)
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all
obligations and liabilities in respect of leases required in conformity
with generally accepted accounting principles to be accounted for as
capitalized lease obligations on our balance
sheet;
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(4)
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all
obligations and other liabilities under any lease or related document in
connection with the lease of real property which provides that we are
contractually obligated to purchase or cause a third party to purchase the
leased property and thereby guarantee a minimum residual value of the
leased property to the lessor and our obligations under the lease or
related document to purchase or to cause a third party to purchase the
leased property;
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(5)
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all
obligations with respect to an interest rate or other swap, cap or collar
agreement or other similar instrument or agreement or foreign currency
hedge, exchange, purchase or other similar instrument or
agreement;
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(6)
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all
direct or indirect guaranties or similar agreements in respect of, and our
obligations or liabilities to purchase, acquire or otherwise assure a
creditor against loss in respect of, indebtedness, obligations or
liabilities of others of the type described in (1) through (5)
above;
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(7)
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any
indebtedness or other obligations described in (1) through (6) above
secured by any mortgage, pledge, lien or other encumbrance existing on
property which is owned or held by us;
and
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(8)
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any
and all refinancings, replacements, deferrals, renewals, extensions and
refundings of, or amendments, modifications or supplements to, any
indebtedness, obligation or liability of the kind described in clauses (1)
through (7) above.
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·
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indebtedness that expressly
provides that it shall not be senior in right of payment to subordinated
debt securities or expressly provides that it is on the same basis or
junior to subordinated debt
securities;
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·
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our indebtedness to any of our
majority-owned subsidiaries;
or
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·
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subordinated debt
securities.
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·
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the title of the debt
warrants;
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·
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the offering price for the debt
warrants, if any;
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·
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the aggregate number of the debt
warrants;
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·
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the designation and terms of the
debt securities, including any conversion rights, purchasable upon
exercise of the debt
warrants;
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·
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if applicable, the date from and
after which the debt warrants and any debt securities issued with them
will be separately
transferable;
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·
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the principal amount of debt
securities that may be purchased upon exercise of a debt warrant and the
exercise price for the warrants, which may be payable in cash, securities
or other property;
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·
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the dates on which the right to
exercise the debt warrants will commence and
expire;
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·
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if applicable, the minimum or
maximum amount of the debt warrants that may be exercised at any one
time;
|
|
·
|
whether the debt warrants
represented by the debt warrant certificates or debt securities that may
be issued upon exercise of the debt warrants will be issued in registered
or bearer form;
|
|
·
|
information
with respect to book-entry procedures, if
any;
|
|
·
|
the
currency or currency units in which the offering price, if any, and the
exercise price are payable;
|
|
·
|
if applicable, a discussion of
material U.S. federal income tax
considerations;
|
|
·
|
the antidilution provisions of
the debt warrants, if any;
|
|
·
|
the redemption or call
provisions, if any, applicable to the debt
warrants;
|
|
·
|
any provisions with respect to
the holder’s right to require us to repurchase the warrants upon a change
in control or similar event;
and
|
|
·
|
any additional terms of the debt
warrants, including procedures, and limitations relating to the exchange,
exercise and settlement of the debt
warrants.
|
|
·
|
the title of the
warrants;
|
|
·
|
the offering price for the
warrants, if any;
|
|
·
|
the aggregate number of
warrants;
|
|
·
|
the designation and terms of the
common stock or preferred stock that may be purchased upon exercise of the
warrants;
|
|
·
|
if applicable, the designation
and terms of the securities with which the warrants are issued and the
number of warrants issued with each
security;
|
|
·
|
if applicable, the date from and
after which the warrants and any securities issued with the warrants will
be separately transferable;
|
|
·
|
the number of shares of common
stock or preferred stock that may be purchased upon exercise of a warrant
and the exercise price for the
warrants;
|
|
·
|
the dates on which the right to
exercise the warrants shall commence and
expire;
|
|
·
|
if applicable, the minimum or
maximum amount of the warrants that may be exercised at any one
time;
|
|
·
|
the currency or currency units in
which the offering price, if any, and the exercise price are
payable;
|
|
·
|
if applicable, a discussion of
material U.S. federal income tax
considerations;
|
|
·
|
the antidilution provisions of
the warrants, if any;
|
|
·
|
the redemption or call
provisions, if any, applicable to the
warrants;
|
|
·
|
any provisions with respect to
holder’s right to require us to repurchase the warrants upon a change in
control or similar event;
and
|
|
·
|
any additional terms of the
warrants, including procedures, and limitations relating to the exchange,
exercise and settlement of the
warrants.
|
|
·
|
to vote, consent or receive
dividends;
|
|
·
|
to receive notice as stockholders
with respect to any meeting of stockholders for the election of our
directors or any other matter;
or
|
|
·
|
to exercise any rights as
stockholders of the Company.
|
|
·
|
the benefits to be derived from
relationships with our
collaborators;
|
|
·
|
any breach of his or her duty of
loyalty to the registrant or its
stockholders;
|
|
·
|
acts or omissions not in good
faith which involve intentional misconduct or a knowing violation of
law;
|
|
·
|
the payment of dividends or the
redemption or purchase of stock in violation of Delaware law;
or
|
|
·
|
any transaction from which the
director derived an improper personal
benefit.
|
|
·
|
Annual
Report on Form 10-K for the fiscal year ended December 31, 2009,
filed on March 17, 2010,
as amended by Amendment No. 1 to Annual Report on Form 10-K/A filed on
April 30, 2010;
|
|
·
|
Quarterly
Report on Form 10-Q for the quarter ended March 31, 2010, filed
on April 30, 2010;
|
|
·
|
Current
Reports on Form 8-K filed on January 27, 2010 and April 6, 2010;
and
|
|
·
|
The
description of our common stock set forth in the registration statement on
Form 8-A registering our common stock under Section 12 of the Exchange
Act, which was filed with the SEC on September 20,
2006.
|
SEC
registration fee
|
$ | 7,130 | ||
Legal
fees and expenses
|
$ | 75,000 | ||
Accounting
fees and expenses
|
$ | 25,000 | ||
Printing
and engraving expenses
|
$ | 25,000 | ||
Miscellaneous
expenses
|
$ | 25,000 | ||
Blue
sky fees and expenses
|
$ | 25,000 | ||
$ | 182,130 |
Exhibit No.
|
Description of Document
|
|
1.1 ***
|
Underwriting
Agreement
|
|
4.1
|
Amended
and Restated Certificate of Incorporation, as filed with the Delaware
Secretary of State on April 26, 2006 (incorporated by reference to Exhibit
3.1 to the Registrant’s Current Report of Form 8-K filed April 26,
2006)
|
|
4.2
|
Certificate
of Merger dated September 13, 2005, relating to the merger of ZIO
Acquisition Corp. with and into ZIOPHARM, Inc. (incorporated by reference
to Exhibit 3.1 to the Registrant’s Form 8-K filed September 19,
2005)
|
|
4.3
|
Certificate
of Ownership of the Registrant (formerly “EasyWeb, Inc.”) dated as of
September 14, 2005, relating the merger of ZIOPHARM, Inc. with and into
the Registrant, and changing the Registrant’s corporate name from EasyWeb,
Inc. to ZIOPHARM Oncology, Inc. (incorporated by reference to Exhibit 3.2
to the Registrant’s Form 8-K filed September 19,
2005)
|
|
4.4
|
Bylaws,
as amended to date (incorporated by reference to Exhibit 3.3 to the
Registrant’s Form 8-K filed September 19, 2005)
|
|
4.5
|
Specimen
common stock certificate (incorporated by reference to Exhibit 4.1 to the
Registrant’s Registration Statement on Form SB-2 [SEC File No. 333-129020]
filed October 14, 2005)
|
|
4.6 ***
|
Specimen
preferred stock certificate
|
|
4.7 ***
|
Form
of Debt Security
|
|
4.8
**
|
Form
of Indenture between the Registrant and one or more trustees to be
named
|
|
4.9 ***
|
Form
of Warrant
|
|
4.10***
|
Form
of Warrant Agreement
|
|
5.1
**
|
Legal
opinion of Maslon Edelman Borman & Brand, LLP
|
|
12.1
**
|
Statement
of Computation of Ratio of Earnings to Fixed
Charges
|
|
23.1
*
|
Consent
of Independent Registered Public Accounting Firm - Caturano and Company,
P.C.
|
|
23.2
**
|
Consent
of Maslon Edelman Borman & Brand, LLP (included as part of Exhibit
5.1)
|
|
24.1
**
|
Power
of Attorney
|
|
25.1****
|
|
Statement
of Eligibility of Trustee on
Form T-1
|
* | Filed herewith. |
** | Previously filed. |
***
|
To
be filed by amendment or as an exhibit to a report pursuant to
Section 13(a), 13(c) or 15(d) of the Exchange
Act.
|
****
|
To
be filed pursuant to Section 305(b)(2) of the Trust Indenture Act at
the time of an offering of debt
securities.
|
ZIOPHARM
Oncology, Inc.
|
||
By:
|
/s/
Richard E. Bagley
|
|
Richard
E. Bagley
|
||
President,
Treasurer and Chief Operating
Officer
|
Name
|
Title
|
Date
|
||
*
|
Director
and Chief Executive Officer
|
May
10, 2010
|
||
Jonathan
Lewis
|
(Principal
Executive Officer)
|
|||
/s/
Richard E. Bagley
|
Director,
President, Treasurer and Chief Operating
Officer
|
May
10, 2010
|
||
Richard
E. Bagley
|
(Principal
Accounting and Financial Officer)
|
|||
|
|
|||
*
|
Director
|
May
10, 2010
|
||
George
B. Abercrombie
|
||||
|
||||
*
|
Director
|
May
10, 2010
|
||
Murray
Brennan
|
||||
|
||||
*
|
Director
|
May
10, 2010
|
||
James
Cannon
|
||||
|
||||
*
|
Director
|
May
10, 2010
|
||
Timothy
McInerney
|
||||
|
||||
*
|
Director
|
May
10, 2010
|
||
Wyche
Fowler, Jr.
|
||||
|
||||
|
Director
|
|
||
Gary
S. Fragin
|
||||
|
||||
*
|
|
Director
|
May
10, 2010
|
|
Michael
Weiser
|
|
|
* By: |
/s/
Richard E. Bagley
|
|
|||
Richard
E. Bagley, Attorney-in-fact
|
|
||||
|
|
Exhibit No.
|
Description of Document
|
|
1.1 ***
|
Underwriting
Agreement
|
|
4.6 ***
|
Specimen
preferred stock certificate
|
|
4.7 ***
|
Form
of Debt Security
|
|
4.8
**
|
Form
of Indenture between the Registrant and one or more trustees to be
named
|
|
4.9 ***
|
Form
of Warrant
|
|
4.10
***
|
Form
of Warrant Agreement
|
|
5.1
**
|
Legal
opinion of Maslon Edelman Borman & Brand, LLP
|
|
12.1
**
|
Statement
of Computation of Ratio of Earnings to Fixed
Charges
|
|
23.1
*
|
Consent
of Independent Registered Public Accounting Firm - Caturano and Company,
P.C.
|
|
23.2
**
|
Consent
of Maslon Edelman Borman & Brand, LLP (included as part of Exhibit
5.1)
|
|
24.1
**
|
Power
of Attorney
|
|
25.1
****
|
|
Statement
of Eligibility of Trustee on
Form T-1
|
* | Filed herewith. |
** | Previously filed. |
***
|
To
be filed by amendment or as an exhibit to a report pursuant to
Section 13(a), 13(c) or 15(d) of the Exchange
Act.
|
****
|
To
be filed pursuant to Section 305(b)(2) of the Trust Indenture Act at
the time of an offering of debt
securities.
|
May
10, 2010
|
Alan
Gilbert
Direct
Phone: 612-672-8381
Direct
Fax: 612-642-8381
Alan.Gilbert@maslon.com
|
Re:
|
ZIOPHARM
Oncology, Inc. (the “Company”)
|
|
Registration
Statement on Form S-3/A
|
|
Filed
April 30, 2010
|
|
File
Number 333-166444
|
|
1.
|
We
note that you filed a Form 8-K on January 27, 2010 and a Form 10-K/A on
April 30, 2010, both of which are not incorporation by reference into your
Form S-3. Please amend your Form S-3 to incorporate by
reference these two filings. Please see Item 12(a) of Form S-3
for additional information.
|
|
Contemporaneously
with the filing of this correspondence, the Company has filed with the
Commission an amendment to the Registration Statement on Form S-3/A
incorporating by reference into the Registration Statement the two filings
identified above. In addition, the Registration Statement has
been amended to update the closing price of the Company’s stock and the
number of shares of the Company’s common stock issued and outstanding,
each as of May 7, 2010. See the cover page and page 6,
respectively.
|
Regards, | |||
|
|
/s/ Alan M. Gilbert | |
Alan M. Gilbert, Esq. | |||
cc:
(via email):
|
Dr.
Jonathan Lewis
|
Richard Bagley | |
Tyler Cook | |
Kevin Lafond |