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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficiency of CD123-Targeted CAR-T in Treating Patients with relapsed/refractory AML


Clinical Trial Description

The relapsed/refractory AML patients will receive FC (F,Fludarabine,C,Cyclophosphamide) chemotherapy followed by infusion of allogenic or autologous CD123-Targeted CAR-T cells.No graft-versus-host disease (GVHD) prevention will be conducted before or after infusion. Dose-limiting toxicity,incidence of adverse events and disease response will be detected post-infusion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03556982
Study type Interventional
Source The Affiliated Hospital of the Chinese Academy of Military Medical Sciences
Contact HUISHENG AI
Phone 8610-66947126
Email HUISHNGAI@163.COM
Status Recruiting
Phase Phase 1/Phase 2
Start date March 1, 2018
Completion date March 1, 2020

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