Bristol Myers Squibb Gets FDA Approval for Myeloma Treatment

By Dean Seal


Bristol Myers Squibb received approval for Zenbexus to be used as a treatment for multiple myeloma when combined with certain other drugs.

The biopharmaceutical manufacturer said Thursday the Food and Drug Administration approved Zenbexus, the brand name for iberdomide, in combination with daratumumab and hyaluronidase-fihj and dexamethasone, for adult patients with multiple myeloma who have received at least one prior line of therapy.

The company is still awaiting full approval for this indication, which is contingent upon verification and description of clinical benefit in the confirmatory trial, Bristol Myers Squibb said.

The drub combination was observed to have a safety profile that was in line with expectations.


Write to Dean Seal at dean.seal@wsj.com


(END) Dow Jones Newswires

August 13, 2026 17:49 ET (21:49 GMT)

Copyright (c) 2026 Dow Jones & Company, Inc.

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