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Astellas Highlights Progress to Advance Care of Patients with Genitourinary Cancers at ASCO-GU Annual Meeting
Date:2/13/2013

vozanib versus patients who received sorafenib in the TIVO-1 study.  Additionally, four posters with tivozanib data regarding the safety and efficacy profile of tivozanib will also be presented at the meeting. A new drug application (NDA) for tivozanib, an investigational agent,  is currently under review by the FDA for the treatment of patients with advanced renal cell carcinoma.

"We applaud companies such as Astellas that are committed to developing medicines for difficult-to-treat cancers," said Helen Miller , LCSW, CancerCare CEO. "We share their commitment to put cancer patients first."

About Astellas

Astellas Pharma US, Inc., located in Northbrook, Illinois, is a U.S. affiliate of Tokyo-based Astellas Pharma Inc. Astellas is a pharmaceutical company dedicated to improving the health of people around the world through the provision of innovative and reliable pharmaceutical products. The organization is committed to becoming a global category leader in oncology, and has several oncology products on the market and compounds in development. Astellas is proud to be an award recipient of the CEO Gold Standard Accreditation from the CEO Roundtable on Cancer. For more information on Astellas Pharma Inc., please visit our website at www.astellas.us.

About XTANDI® 

XTANDI® (enzalutamide) capsules is an oral, once-daily androgen receptor inhibitor. XTANDI was approved by the FDA on August 31, 2012 for the treatment of metastatic castration-resistant prostate cancer for patients who have previously received docetaxel (chemotherapy). A Marketing Authorization Application for XTANDI is currently under review by the European Medicines Agency (EMA).

The efficacy and safety of XTANDI were assessed in the randomized, placebo-controlled, global phase 3 AFFIRM clinical trial. A tota
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SOURCE Astellas Pharma US, Inc.
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