Late Breaking News
Stivarga Approved for Some Stromal Tumors After Use of First-Line Therapies
- Categorized in: April 2013, Department of Defense (DoD), Department of Veterans Affairs (VA), FDA News, News, Oncology, Pharmacy
WAYNE, NJ - Tthe U.S. Food and Drug Administration (FDA) has approved Bayer's Stivarga (regorafenib) tablets to treat patients with locally advanced, unresectable or metastatic gastrointestinal stromal tumor (GIST) who have been previously treated with imatinib mesylate and sunitinib malate, according to Bayer HealthCare and Onyx Pharmaceuticals, Inc. In September 2012, Stivarga was approved for the treatment of patients with metastatic colorectal cancer (mCRC) who have been previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-VEGF therapy, and, if KRAS wild type, an anti-EGFR therapy. Stivarga is a Bayer compound developed by Bayer and jointly promoted by Bayer and Onyx in the United States.