U.S. Markets
Bristol-Myers-Squibb (BMY) says the US FDA has accepted a New Drug Application for mezigdomide in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma
StockNow breaking-news AI analysis
BMY's mezigdomide NDA acceptance marks a critical step for its CELMoD platform. Phase 3 SUCCESSOR-2 data shows a 52% risk reduction in RRMM progression, positioning mezigdomide as a potential new oral standard.
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