Amgen And Allergan Submit Biosimilar Biologics License Application For ABP 980 To US Food And Drug Administration

Filing for ABP 980, a Biosimilar Candidate to Herceptin® (trastuzumab), Supported by Phase 3 Data in Patients With HER2-Positive Early Breast Cancer THOUSAND OAKS, Calif., July 31, 2017 /PRNewswire/ -- Amgen (NASDAQ:AMGN) and Allergan plc. (NYSE:AGN) today announced the submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for ABP 980, a biosimilar candidate to Herceptin® (trastuzumab). Amgen and Allergan are collaborating on four oncology biosimilar medicines, including ABP 980 which is the second to be submitted for FDA approval. "The submission of ABP 980 for FDA review is an exciting milestone and speaks to our joint commitment with Al...
Source: Amgen News Release - Category: Pharmaceuticals Tags: Uncategorized Source Type: news