ompany engaged
in the development and commercialization of a diverse,
risk-sensitive portfolio of in-licensed cancer drugs to address
unmet medical needs. The Company applies new insights from
molecular and cancer biology to understand the efficacy and safety
limitations of approved and developmental cancer therapies and
identifies proprietary and related molecules for better patient
treatment. For more information, visit www.ziopharm.com.
Forward-Looking Safe Harbor Statement:
This 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, and risks related to the Company's ability to protect its
intellectual property and its reliance on third parties to develop
its product candidates. The Company assumes no obligation to update
these forward-looking statements, except as required by law.
ZIOP-G
Contact
For ZIOPHARM Oncology, Inc.
Investors:
Suzanne McKenna, 646-214-0703
smckenna@ziopharm.com
or
Media:
Tina Posterli, 91
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Page: 1 2 3 4 Related medicine technology :1.
ZIOPHARM Presents Data Highlighting Oral ZIO-101 at AACR2.
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Positive ZIO-201 Interim Phase II Sarcoma Data Presented at
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Ablynx Announces Interim Results of First Nanobody Phase I Study of
ALX-0081 (ANTI-VWF)5.
Based on Up to 6 Years of Follow-Up, Biovest Announces Favorable
Interim Blinded Data for Fast-Tracked Pivotal Phase 3 Clinical
Trial of BiovaxID Anti-Cancer Vaccine for Non-Hodgkins Lymphoma6.
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Data on SinuNase in Its Fast-Tracked Pivotal Phase 3 Clinical Trial
for Chronic Sinusitis7.
Pharmacyclics Announces Interim Results From Two Ongoing Phase 2
Trials Supporting Potential of Xcytrin Plus Chemotherapy to Treat
Recurrent Non-Small Cell Lung Cancer8.
Interim Analysis of Crinone Pregnancy Study to Be Published in
American Society for Reproductive Medicine Journal9.
Avalon Pharmaceuticals Announces Positive Interim Results For
AVN944 Phase I Trial10.
Vical Interim Clinical Results Demonstrate Safety and Tolerability
of Inovio Biomedicals Electroporation DNA Delivery Technology11.
Interim Data From RECORD Study Show No Significant Difference
Between Avandia and Standard Therapy in Risk of Cardiovascular
Hospitalization or Death