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Bristol Myers Wins FDA Approval for Zenbexus, Debuting New Myeloma Drug Class

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Bristol Myers Squibb has received FDA approval for Zenbexus, a treatment for advanced multiple myeloma. This marks the debut of a new class of drugs known as CELMoDs, which are designed to target and degrade specific proteins involved in the disease.

The approval is a significant milestone for Bristol Myers, as Zenbexus is the first drug in this novel category to gain clearance from the FDA, expanding treatment options for patients with this challenging blood cancer.

Bristol Myers Squibb

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