Bristol Myers Squibb Receives FDA Approval for First CELMoD Therapy ZENBEXUS for Multiple Myeloma
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The U.S. FDA has granted accelerated approval to Bristol Myers Squibb's first CELMoD therapy, ZENBEXUS™, in combination with Daratumumab and Hyaluronidase for patients with multiple myeloma. This marks a significant milestone as it is the first approval for a new class of protein-degrading drugs targeting this blood cancer.
The approval of ZENBEXUS™ is a notable achievement for Bristol Myers Squibb, particularly following its acquisition of Celgene, which developed the drug. This new treatment option is expected to provide a novel approach for patients facing advanced stages of multiple myeloma.
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“U.S. FDA Grants Accelerated Approval to Bristol Myers Squibb's First CELMoD Therapy ZENBEXUS™, in Combination with Daratumumab and Hyaluroni…”
SEC Filing — U.S. FDA Grants Accelerated Approval to Bristol Myers Squibb's First CELMoD Therapy ZENBEXUS™, in Combination with Daratumumab and Hyaluroni…“<figure><div><img”
biopharma dive — Bristol Myers wins ‘milestone’ FDA approval of myeloma drug acquired from Celgene“The FDA approved a treatment for advanced multiple myeloma made by Bristol Myers Squibb, marking the debut of a new class of drugs for the blood cancer.”
stat news — STAT+: FDA approves Bristol multiple myeloma treatment, marking debut of novel drug class