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FDA Approves Brexucabtagene Autoleucel for R/R B-Cell Precursor ALL

On October 1, 2021, the U.S. Food and Drug Administration (FDA) approved brexucabtagene autoleucel for adult patients with relapsed or refractory (R/R) B-cell precursor acute lymphoblastic leukemia (ALL).

Read the FDA announcement.

Read Kite Pharma's announcement.

Posted 10/4/2021