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TECARTUS® (Brexucabtagene autoleucel)

April 1, 2022April 1, 2022 RR FDA Approvals
Acute Lymphocytic Leukemia

The FDA on October 1, 2021, approved TECARTUS® (Brexucabtagene autoleucel) for adult patients with Relapsed or Refractory B-cell precursor Acute Lymphoblastic Leukemia (ALL). TECARTUS® is a product of Kite Pharma, Inc.

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