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Approval of brexucabtagene autoleucel for adults with relapsed and refractory acute lymphocytic leukemia

2022/05/04 by Noelle V. Frey · 21 citations
Medicine · #CAR-T cell therapy research

paper · pdf · doi:10.1182/blood.2021014892

Abstract

In October 2021, brexucabtagene autoleucel became the first anti-CD19 chimeric antigen receptor T-cell product to receive approval from the Food and Drug Administration to treat adults with relapsed and refractory B-cell acute lymphoblastic leukemia. The approval is based on results from the Zuma-3 trial and significantly widens treatment options for this patient population. In this article, we review outcomes from this study and its implications.

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