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Clinical Trial Summary

The present study evaluates the safety and efficacy of humanized Chimeric antigen receptor T cells (CAR-T) in treating recurrent or refractory B cell malignancy targeting CD19 with a humanized scFv. All participants will receive autologous chimeric antigen receptor engineered T cells.


Clinical Trial Description

CD19 has been extensively evaluated as a therapeutic target for recurrent or refractory B cell malignancy by chimeric antigen receptor T cell therapy, the single chain antibody sequence (scFv) against CD19 derived from a mouse hybridoma was widely employed. However, the immunogenicity of the mouse scFv sequence might be one of the reasons that CAR-T cells cannot persist in vivo for long. In present study investigators replace the mouse-derived scFv with a a humanized one and evaluate its safety and efficacy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02782351
Study type Interventional
Source Xuzhou Medical University
Contact Jiang Cao, M.D., Ph.D.
Phone 8651685802291
Email zimu05067@163.com
Status Recruiting
Phase Phase 1/Phase 2
Start date May 2016
Completion date December 2018

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