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Clinical Trial Summary

Master protocol: The goal of this master clinical study is to test how well the study drug, brexucabtagene autoleucel, works in participants with rare B-cell malignancies: relapsed/refractory Waldenstrom macroglobulinemia (r/r WM) (Substudy A - no longer recruiting), relapsed/refractory Richter transformation (r/r RT) (Substudy B), relapsed/refractory Burkitt lymphoma (r/r BL) (Substudy C and relapsed/refractory hairy cell leukemia (r/r HCL) (Substudy D - no longer recruiting).


Clinical Trial Description

Master protocol: The primary objective of this study is to evaluate the efficacy of brexucabtagene autoleucel in two rare B-cell malignancies. This study will use a basket study design with separate, indication-specific substudies, to investigate r/r RT and r/r BL. After completing the treatment period, all participants will be followed in the post-treatment follow-up period. Thereafter, participants will transition to a separate long-term follow-up study (KT-US-982-5968) to continue follow-up out to 15 years. Substudies A and D have been early terminated by the sponsor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05537766
Study type Interventional
Source Gilead Sciences
Contact Medical Information
Phone 844-454-5483(1-844-454-KITE)
Email medinfo@kitepharma.com
Status Recruiting
Phase Phase 2
Start date November 1, 2022
Completion date March 2025

See also
  Status Clinical Trial Phase
Approved for marketing NCT03501615 - An Early Access Programme for Moxetumomab Pasudotox in Relapsed/Refractory Hairy Cell Leukemia