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Clinical Trial Summary

CD19-directed CAR-T cell therapy has shown promising results for the treatment of relapsed or refractory B-cell malignancies; however, a subset of patients relapse due to the loss of CD19 in tumor cells. CD38 CAR-T cells can recognize and kill the CD19 negative malignant cells through recognition of CD38. This is a phase 1/2 study designed to determine the safety of the gene-edited specificity CD38 CAR-T cells and the feasibility of making enough to treat patients with relapsed B-cell acute lymphoblastic leukemia after CD19 CAR-T adoptive cellular immunotherapy.


Clinical Trial Description

1. PRIMARY OBJECTIVES:

1. To evaluate the feasibility and safety of specificity CD38 CAR-T cells in patients with relapsed or refractory leukemia and lymphoma.

2. To evaluate the duration of in vivo persistence of adoptively transferred T cells, and the phenotype of persisting T cells.

Real Time polymerase chain receptor (RT-PCR) and Flow cytometry(FCM) analysis of PB,BM and lymph node will be used to detect and quantify survival of CD38 CAR-T cells over time.

2. SECONDARY OBJECTIVES:

1. For patients with detectable disease, measure anti-tumor response due to specificity CD38 CAR-T cell infusions.

2. The CAR-T cells will be administered by i.v. injection over 20-30 minutes as a using Day 0: 1-5x10e6/kg total dose on day 0. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03754764
Study type Interventional
Source Chinese PLA General Hospital
Contact Hejin Jia
Phone 86-10-55499341
Email PLAGH@QQ.COM
Status Recruiting
Phase Phase 1/Phase 2
Start date November 23, 2018
Completion date November 23, 2022