BRIEF-U.S. FDA Accepts Bristol Myers Squibb’S Supplemental BLA For Opdivo® Plus Yervoy®

Reuters
02-24
BRIEF-U.S. FDA Accepts Bristol Myers Squibb’S Supplemental BLA For Opdivo® Plus Yervoy®

Feb 24 (Reuters) - Bristol-Myers Squibb Co BMY.N:

  • U.S. FOOD AND DRUG ADMINISTRATION ACCEPTS BRISTOL MYERS SQUIBB’S SUPPLEMENTAL BIOLOGICS LICENSE APPLICATION FOR OPDIVO® PLUS YERVOY® FOR PATIENTS WITH UNRESECTABLE OR METASTATIC MICROSATELLITE INSTABILITY-HIGH OR MISMATCH REPAIR DEFICIENT...

  • BRISTOL-MYERS SQUIBB CO - FDA ASSIGNS TARGET ACTION DATE OF JUNE 23, 2025

Source text: ID:nBw2tnHFDa

Further company coverage: BMY.N

((Reuters.Briefs@thomsonreuters.com;))

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