Relmacabtagene Autoleucel in Patients With LBCL

Status Recruiting

Clinical Trial Summary

To evaluate the efficacy and safety of Relmacabtagene autoleucel for the treatment of adult patients with relapsed or refractory (r/r) large B-cell lymphoma (LBCL) in real-world

Clinical Trial Description

This is a post-marketing, multicenter, observational real-world study, including prospective and retrospective studies. The purpose of this study is to collect efficacy and safety data over a 6-month period following treatment of adult patients with r/r LBCL with Relmacabtagene autoleucel. The treating physicians in the study will determine the most appropriate diagnostic and therapeutic regimen for their patients based on clinical practice.There will be no therapeutic intervention as a result of this study. There will be no subgroups of any kind in this study, and subgroup analyses will be performed based on the actual data collected during the analysis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06142175
Study type	Observational
Source	Shanghai Ming Ju Biotechnology Co., Ltd.
Contact	Medical JWCAR029, PhD
Phone	+86 21 50464201
Email	JWCAR029Medical@jwtherapeutics.com
Status	Recruiting
Phase
Start date	December 28, 2022
Completion date	December 31, 2024

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See also
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