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 aimed at treating this advanced blood cancer.
The approval of ZENBEXUS is a pivotal moment for Bristol Myers Squibb, showcasing the company's commitment to advancing treatment options for multiple myeloma. The drug's introduction is expected to provide new hope for patients facing this challenging condition.
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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