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FDA grants priority review of Amgen's panitumumab for colorectal cancer
By Lisa Kerner
Charlotte, N.C., June 12 - Amgen Inc. said the Food and Drug Administration has granted priority review to its Biologic License Application for panitumumab, an investigational fully human monoclonal antibody for the treatment of metastatic colorectal cancer patients who have failed prior chemotherapy.
Panitumumab received fast track designation from the FDA in July 2005. It is being evaluated in clinical trials as both a monotherapy and with other agents for the treatment colorectal, lung and head and neck cancers, according to a company news release.
Amgen is a biotechnology company located in Thousand Oaks, Calif.
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