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BMS bags first FDA approval for CELMoD franchise with Zenbexus multiple myeloma nod

FiercepharmaView source article

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FDA approves Bristol Myers Squibb's Zenbexus, first CELMoD drug for multiple myeloma

The FDA has approved Zenbexus (iberdomide) for multiple myeloma treatment, marking the first approval in the novel CELMoD drug class that uses targeted protein degradation. Bristol Myers Squibb acquired the therapy through its Celgene acquisition and is positioning it as a successor to its legacy myeloma products.

Aug 14, 2026·4 sourcesFDA drug approvalCancer treatment breakthroughsCancer treatment
FDA approves Bristol Myers Squibb's Zenbexus, first CELMoD drug for multiple myeloma
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Other sources for this story

Statnews

FDA approves Bristol multiple myeloma treatment, marking debut of novel drug class

Biopharmadive

Bristol Myers wins ‘milestone’ FDA approval of myeloma drug acquired from Celgene

Medcitynews

Bristol Myers Squibb Protein Degrader Wins First-in-Class FDA Nod in Multiple Myeloma - MedCity News