Tecartus

Drug

Also known as: KTE-X19

Drug Profile

Tecartus (brexucabtagene autoleucel) is a CD19-directed genetically modified autologous T-cell immunotherapy used in relapsed or refractory mantle cell lymphoma and B-cell precursor acute lymphoblastic leukemia in adults. FDA product records list ongoing regulatory updates through April 2026.

Drug Class
CD19-directed genetically modified autologous T-cell immunotherapy (CAR-T cell therapy)
Approval Status
FDA approved (multiple approval letters listed through April 1, 2026)
Mechanism of Action
Autologous CD19-directed genetically modified T-cell immunotherapy targeting CD19-expressing malignant B cells.
Brand Names
  • TECARTUS
Indications
  • \Adult relapsed or refractory mantle cell lymphoma\
  • \Adult relapsed or refractory B-cell precursor acute lymphoblastic leukemia\

Related News

Related Clinical Trials

NCT ID Title Status Phase
NCT06144606

Study of KTE-X19 in Minimal Residual Disease (MRD) Positive B-Cell Acute Lymphoblastic Leukemia (B-ALL)

RECRUITING PHASE2
NCT03642626

MT2017-45: CAR-T Cell Therapy for Heme Malignancies

ACTIVE_NOT_RECRUITING PHASE2