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FDA Approves Brexucabtagene Autoleucel for Relapsed or Refractory B-cell Precursor Acute Lymphoblastic Leukemia

Oncology Practice Insider

On October 1, 2021, the Food and Drug Administration approved brexucabtagene autoleucel (Tecartus, Kite Pharma, Inc.) for adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). Read more