Study Evaluating Brexucabtagene Autoleucel (KTE-X19) in Pediatric and Adolescent Participants With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia or Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma (ZUMA-4)

  • STATUS
    Recruiting
  • End date
    Aug 23, 2038
  • participants needed
    116
  • sponsor
    Kite, A Gilead Company
Updated on 7 October 2022
lymphoid leukemia
fludarabine
cyclophosphamide
tyrosine
lymphoma
hodgkin's disease
residual disease
pleural effusion
leukemia
b-cell acute lymphoblastic leukemia
residual tumor
oximetry
b-cell lymphoma
left ventricular fractional shortening

Summary

The primary objectives of this study are to evaluate the safety and efficacy of brexucabtagene autoleucel (KTE-X19) in pediatric and adolescent participants with relapsed/refractory (r/r) B-precursor acute lymphoblastic leukemia (ALL) or relapsed or refractory (r/r) B-cell non-Hodgkin lymphoma (NHL).

Details
Condition Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia, Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma
Treatment cyclophosphamide, Fludarabine, KTE-C19, KTE-X19, Brexucabtagene Autoleucel (KTE-X19)
Clinical Study IdentifierNCT02625480
SponsorKite, A Gilead Company
Last Modified on7 October 2022

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