Full Press Release Details
ANNOUNCES COMMENCEMENT OF PUBLIC OFFERING
NEW YORK, NY - December 3,
2009 - ZIOPHARM Oncology, Inc. (NASDAQ: ZIOP) announced today that it
intends to offer shares of its common stock and warrants to purchase shares of
its common stock in a public offering. JMP Securities LLC and Rodman &
Renshaw, LLC are acting as co-lead managers for the offering.
Company plans to use net proceeds from this offering for general corporate
purposes, which may include ongoing clinical development of its three product
candidates, palifosfamide (ZymafosTM or
ZIO-201), darinaparsin (ZinaparTM or
ZIO-101), and indibulin (ZybulinTM or
offering is being made pursuant to an effective shelf registration statement
previously filed with the Securities and Exchange Commission (File No.
333-161453). A prospectus supplement relating to the offering will be
filed with the Securities and Exchange Commission. When available, copies of the
prospectus supplement relating to this offering may be obtained by contacting
JMP Securities LLC at Equity Syndicate, 600 Montgomery Street, Suite 1100, San
Francisco, CA 94111; (415) 835-8900.
press release does not constitute an offer to sell, or the solicitation of an
offer to buy, shares of common stock and warrants. Furthermore, ZIOPHARM
Oncology, Inc. will not sell any of the common stock or warrants and has been
advised by JMP Securities LLC that the underwriters and their affiliates will
not sell any of the common stock or warrants in any state or jurisdiction in
which such offer, solicitation or sale would be unlawful prior to registration
or qualification of the securities under the securities laws of any such state
ZIOPHARM Oncology, Inc.:
biopharmaceutical company engaged in the development and commercialization of a
diverse portfolio of cancer drugs. The Company is currently focused on three
ZIO-201) references a novel composition (tris formulation) that is the
functional active metabolite of ifosfamide, a standard of care for treating
sarcoma, lymphoma, testicular, and other cancers. Palifosfamide delivers
only the cancer fighting component of ifosfamide. It is expected to overcome the
resistance seen with ifosfamide and cyclophosphamide, two of the most commonly
used alkylating drugs used to treat certain cancers. Palifosfamide does not have
the toxic metabolites of ifosfamide that cause the debilitating side effects of
"fuzzy brain" (encephalopathy) and severe bladder inflammation.
organic arsenic being developed for the treatment of various hematologic and
solid cancers. Preclinical and clinical studies to date have demonstrated that
darinaparsin is considerably less toxic than inorganic arsenic, particularly
with regard to cardiac toxicity.
novel, oral tubulin binding agent that targets both mitosis and cancer cell
migration. Indibulin is expected to have several potential benefits,
including oral dosing, application in multi-drug resistant tumors, no neuropathy
and minimal overall toxicity.
In multiple Phase I trials in cancer patients, oral indibulin has been
administered both as a single agent and in combination with favorable activity
and a promising safety profile that does not include the neurotoxicity seen with
all of the other classes of tubulin binding agents.
operations are located in Boston, MA with an executive office in New York.
Further information about ZIOPHARM may be found at www.ziopharm.com.
Safe Harbor Statement:
press release contains forward-looking statements for ZIOPHARM Oncology, Inc.
that involve risks and uncertainties that could cause the Company's actual
results to differ materially from the anticipated results and expectations
expressed in these forward-looking statements. These statements are based on
current expectations, forecasts and assumptions that are subject to risks and
uncertainties, which could cause actual outcomes and results to differ
materially from these statements. Among other things, there can be no assurance
that any of the Company's development efforts relating to its product candidates
will be successful, or such product candidates will be successfully
commercialized. Other risks that affect forward-looking information contained in
this press release include the possibility of being unable to obtain regulatory
approval of the Company's product candidates, the risk that the results of
clinical trials may not support the Company's claims, risks related to the
Company's ability to protect its intellectual property and its reliance on third
parties to develop its product candidates, risks related to the sufficiency of
existing capital reserves to fund continued operations for a particular amount
of time and uncertainties regarding the Company's ability to obtain additional
financing to support its operations thereafter. The Company assumes no
obligation to update these forward-looking statements, except as required by
Noonan Communications, LLC
Communications Group