SPEAR (Study of Picoplatin Efficacy After Relapse),
in small cell lung cancer. This registrational trial is being conducted
under a Special Protocol Assessment (SPA) from the U.S. Food and Drug
Administration and is evaluating overall survival as the primary endpoint.
The Company also is evaluating intravenous picoplatin in two ongoing Phase
2 clinical trials for the treatment of hormone-refractory prostate cancer
and metastatic colorectal cancer. Oral picoplatin is being evaluated in a
Phase 1 clinical trial in solid tumors. Picoplatin has not been approved by
any regulatory authority for use in humans.
About Poniard Pharmaceuticals
Poniard Pharmaceuticals, Inc. is a biopharmaceutical company focused on
the development and commercialization of innovative oncology products to
impact the lives of people with cancer. Picoplatin, the Company's lead
platform product candidate, is a new generation platinum therapy with an
improved safety profile relative to existing platinum-based cancer
therapies. Picoplatin is designed to overcome platinum resistance
associated with chemotherapy in solid tumors, and is being studied in
multiple cancer indications, combinations and formulations. Clinical trials
of intravenous picoplatin include a Phase 3 trial in small cell lung cancer
and Phase 2 trials in metastatic colorectal and hormone-refractory prostate
cancers, as well as a clinical trial of oral picoplatin in solid tumors.
Picoplatin has not been approved by any regulatory authority for use in
humans. For additional information please visit http://www.poniard.com.
This release contains forward-looking statements, including statements
regarding the Company's business objectives and strategic goals, drug
development plans, results of clinical trials and the potential safety and
efficacy of its products in development. The Company's actual results may
differ materially from those indicated in these forward-lo
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SOURCE Poniard Pharmaceuticals, Inc. Copyright©2008 PR Newswire. All rights reserved | |
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