13 August 2026news.bms.com

FDA Accelerated Approval for BMS CELMoD ZENBEXUS in Multiple Myeloma

SigSignificance3.65SenSentiment+7.20EnvEnvironment0.00SocSocial+5.25GovGovernance-0.30

The FDA approved Bristol Myers Squibb’s ZENBEXUS (iberdomide), the first FDA-approved CELMoD, for adult multiple myeloma patients who have had at least one prior line including a proteasome inhibitor and an immunomodulatory agent. It is used with daratumumab, hyaluronidase and dexamethasone, with boxed warnings for embryo-fetal toxicity and thromboembolism; full approval depends on confirmatory trials.

Coverage (1)

U.S. FDA Grants Accelerated Approval to Bristol Myers Squibb's First CELMoD Therapy ZENBEXUS™, in Combination with Daratumumab and Hyaluronidase (news.bms.com)

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