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Clinical Trial Summary

The primary objectives of this study are: Cohort 1: to provide access to brexucabtagene autoleucel (KTE-X19) for individuals with relapsed or refractory (r/r) mantle cell lymphoma (MCL) until KTE-X19 is commercially available Cohort 2: To provide access to KTE-X19 for individuals with r/r MCL whose commercially manufactured product did not meet commercial release specification(s)


Clinical Trial Description

This is an open-label, expanded access study of KTE-X19 for the treatment of individuals with r/r B-cell malignancies. The study will consist of 2 cohorts as indicated below: Cohort 1 will enroll individuals prior to commercial availability of KTE-X19 for the proposed indication. Cohort 2 will enroll individuals after KTE-X19 becomes commercially available in cases when KTE-X19 does not meet commercial release specification(s). The participants who received an infusion of KTE-X19 will be provided the opportunity to transition to a separate long-term follow-up (LTFU) study, KT-US-982-5968. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04162756
Study type Expanded Access
Source Gilead Sciences
Contact
Status Approved for marketing
Phase