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Biologics

US Food and Drug Administration approves first CAR-T treatment for multiple myeloma

by Megha Satyanarayana
April 3, 2021 | A version of this story appeared in Volume 99, Issue 12
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Most Popular in Pharmaceuticals

 

A photo of an infusion bag of Abecma.
Credit: Bristol Myers Squibb
Abecma is administered by infusion.

The US Food and Drug Administration has approved Abecma, the first chimeric antigen receptor T-cell (CAR-T) product for the treatment of multiple myeloma. Unlike other CAR-T treatments, which recognize a cancer marker called CD19, Abecma, from Bristol Myers Squibb and Bluebird Bio, recognizes a cancer marker called B-cell maturation antigen on the surface of multiple myeloma cells. It will be a treatment option for people who have not responded to four or more other therapies.

Chemical & Engineering News
ISSN 0009-2347
Copyright © 2024 American Chemical Society

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