August 14, 2026
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The FDA has granted accelerated approval to the first cereblon E3 ligase modulation therapy for patients with multiple myeloma.Iberdomide (Zenbexus, Bristol Myers Squibb), in combination with daratumumab and hyaluronidase-fihj (Darzalex Faspro, Janssen) and dexamethasone, received approval for adults with multiple myeloma who underwent at least one prior line of therapy including a proteasome
August 14, 2026
2 min read
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Bristol Myers Squibb Gets FDA Nod For Myeloma Treatment - Bristol-Myers Squibb (NYSE:BMY)

FDA Approves First CELMoD Drug for Multiple Myeloma

U.S. FDA Grants Accelerated Approval to Bristol Myers Squibb's First CELMoD Therapy ZENBEXUS™, in Combination with Daratumumab and Hyaluronidase-fihj and Dexamethasone (ZDd) for Patients with Multiple Myeloma, as Early as First Relapse

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

FDA approves Bristol Myers’ multiple myeloma successor

SFDA becomes first regulatory authority globally to approve registration of 'ZENBEXUS' to treat multiple myeloma in adults

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

Bristol Myers Squibb secures FDA approval for Zenbexus (iberdomide), marking the first CELMoD therapy approval.

Iberdomide indicated as part of combination regimen for relapsed or refractory disease

U.S. FDA Grants Accelerated Approval to Bristol Myers Squibb's First CELMoD Therapy ZENBEXUS™, in Combination with Daratumumab…

The clearance of Zenbexus is the first for a group of protein-degrading “CELMoD” medicines that could help Bristol Myers…

FDA approved Bristol Myers Squibb's iberdomide (Zenbexus) for relapsed/refractory multiple myeloma at $29,500/cycle, used with…

Oral mezigdomide's benefit shown in patients mostly refractory to lenalidomide and anti-CD38