U.S. License Holder:
Kite Pharma, Inc.
Date of License:
July-24-2020
Last Update:
Feb-15-2025
FDA-Approved Indications
TECARTUS (brexucabtagene autoleucel) is a CD19-directed genetically modified autologous T cell immunotherapy indicated for the treatment of:
Adult patients with relapsed or refractory mantle cell lymphoma (MCL);
Adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL).