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Medivation Announces Presentation of MDV3100 Clinical Data in Patients With Castration-Resistant Prostate Cancer at 44th American Society of Clinical Oncology Annual Meeting
SAN FRANCISCO (Map) - Session title: New Targeted Strategies for Patients with Prostate Cancer Session date and time: Monday, June 2 at 11:30 a.m. Central Time Abstract title: "Phase 1-2 Study of MDV3100 in Patients with Progressive Castration-Resistant Prostate Cancer (CRPC)" (Abstract #5006) To be presented by: Howard Scher, M.D., chief of the Genitourinary Oncology Service and the D. Wayne Calloway Chair in Urologic Oncology at Memorial Sloan-Kettering Cancer Center in New York, at approximately 12:15 p.m. Central Time Location: W375e Dr. Scher's presentation will include data appearing in the abstract posted today on the ASCO website, as well as additional study data not reflected in the abstract. Medivation's ongoing Phase 1-2 trial of MDV3100 is an open-label dose-escalation study enrolling prostate cancer patients who have failed standard hormonal therapies. The study endpoints include safety, tolerability, pharmacokinetics, effects on serum PSA levels and disease progression. Medivation expects to complete the study and report final top-line results in 2008. About Prostate Cancer Prostate cancer is the most common type of cancer, other than skin cancer,
and the second leading cause of cancer death in American men. More than 1
million men in About Medivation Medivation, Inc. is a biopharmaceutical company focused on the rapid development of novel small molecule drugs to treat serious diseases of the central nervous system and cancers for which there are limited treatment options. Medivation aims to revolutionize the treatment of these diseases and offer hope to critically ill patients and their caregivers. The Company's current clinical development program includes a pivotal and confirmatory Phase 3 trial of Dimebon(TM) in Alzheimer's disease, a Phase 2 clinical trial of Dimebon in patients with mild-to-moderate Huntington's disease, and a Phase 1-2 clinical trial of MDV3100 in patients with castration-resistant (also known as hormone-refractory) prostate cancer. For more information, please visit us at http://www.medivation.com. This press release contains forward-looking statements, including
statements regarding anticipated clinical and regulatory milestones, which are
made pursuant to the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995. Forward-looking statements involve risks and
uncertainties that could cause actual results to differ significantly from
those projected. You are cautioned not to place undue reliance on the
forward-looking statements, which speak only as of the date of this release.
None of the Company's product candidates has been approved for sale,
significant additional animal and human testing is required in order to seek
marketing approval for any of its product candidates, and Medivation cannot
assure you that marketing approval can be obtained for any of its product
candidates. Furthermore, as is typically the case at this stage of the
regulatory review process, the FDA has not yet performed an in-depth review of
Medivation's preclinical and clinical data, so its views remain subject to
change. Medivation's filings with the Securities and Exchange Commission,
including its Annual Report on Form 10-KSB for the year ended (1) American Cancer Society Web Site; Overview: Prostate Cancer (http://www.cancer.org/docroot/CRI/CRI_2_1x.asp?dt=36)
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