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Clinical Trial Summary

This is an open, single-arm, phase I clinical study to evaluate efficacy and safety of chimeric antigen receptor T cell immunotherapy (CAR-T) targeting CD123 in the treatment of Acute Myelocytic Leukemia. A total of 15 patients are planned to be enrolled following up one year.


Clinical Trial Description

Chimeric antigen receptor (CAR)-modified T cells targeted against CD19 have demonstrated unprecedented successes in treating patients with hematopoietic and lymphoid malignancies. Besides CD19, many other molecules such as CD22, CD30,BCMA,CD123, etc. may be potential in developing the corresponding CAR-T cells to treat patients whose tumors expressing those markers. In this study, investigators will evaluate the safety and efficacy of CAR-T targeting CD123 in patients with Acute Myelocytic Leukemia. The primary goal is safety assessment including cytokine storm response and any other adverse effects. In addition, disease status after treatment will also be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03796390
Study type Interventional
Source Hebei Senlang Biotechnology Inc., Ltd.
Contact Peihua Lu, PhD&MD
Phone 008618611636172
Email peihua_lu@126.com
Status Recruiting
Phase Phase 1
Start date December 26, 2018
Completion date June 6, 2021

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