FDA Action Alert: Blueprint, Bristol Myers Squibb, Clovis and Sunovion Blockbusters, BRCA mutation, Clinical Trial Endpoints, FDA, FDA/Regulatory, Gastrointestinal Stromal Tumors, Metastatic Castration-Resistant Prostate Cancer (mCRPC), New Drug Applications, Non-Small Cell Lung Cancer (NSCLC), OFF Episodes, Parkinson's Disease, PDUFA, Sublingual film, Supplemental Biologics License Application, Supplemental New Drug Application (sNDA), Therapeutics Despite the COVID-19 pandemic, the U.S. Food and Drug Administration has managed to stay fairly on track in terms of evaluating new drug and supplemental new drug applications. Here is a look at what is on the schedule for the next two weeks. Read more May 11, 2020/by Andrew Humphreys https://www.pharmalive.com/wp-content/uploads/2020/05/FDA-Action-Alert-for-Blueprint-Bristol-Myers-Squibb-Clovis-and-Sunovion-BioSpace-5-11-20.jpeg 350 625 Andrew Humphreys https://www.pharmalive.com/wp-content/uploads/2020/01/Pharmalive_4c-300x37.png Andrew Humphreys2020-05-11 11:55:552020-05-11 13:37:44FDA Action Alert: Blueprint, Bristol Myers Squibb, Clovis and Sunovion