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Bristol Myers Squibb gains FDA nod for multiple myeloma drug

Bristol Myers Squibb gains FDA nod for multiple myeloma drug
FDA nod for new drug

Bristol Myers Squibb received a significant boost as the U.S. FDA accepted its New Drug Application for an investigational treatment for adult patients with relapsed or refractory multiple myeloma.

The drug has also been granted Breakthrough Therapy Designation, potentially accelerating its development and review process. This move underscores Bristol Myers Squibb's drive toward expanding treatments for challenging conditions in oncology.

This material may contain third-party opinions, none of the data and information on this webpage constitutes investment advice according to our Disclaimer. While we adhere to strict Editorial Integrity, this post may contain references to products from our partners.

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