The goal of this clinical study is to test how well the study drug, brexucabtagene
autoleucel (KTE-X19), works in participants with relapsed/refractory (r/r) mantle cell
lymphoma (MCL).
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT04880434.
Locations matching your search criteria
United States
Texas
Houston
M D Anderson Cancer CenterStatus: Active
Name Not Available
Study KTE-C19-102 (NCT02601313) enrolled participants with r/r MCL who have been treated
with up to 5 prior regimens including a Bruton's tyrosine kinase inhibitor (BTKi) in
Cohort 1 and Cohort 2. However, to fulfill FDA Postmarketing Requirement Cohort 3 is
added to the study. It will include participants with r/r MCL who have been treated with
up to 5 prior regimens but have not received prior therapy with a BTKi.
The primary analysis in Cohort 1 and Cohort 2 is already completed. Data for Cohort 3
will be analyzed separately. Therefore, this separate registration is only for Cohort 3.
After the end of KTE-C19-102, subjects who received an infusion of anti-CD19 CAR T cells
will complete the remainder of the 15-year follow-up assessments in a separate long-term
follow-up study, KT-US-982-5968
Lead OrganizationKite Pharma, Inc.