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Clinical Trial Summary

Assessment of the Safety and Feasibility of Administering T Cells Expressing an Anti-CD123 Chimeric Antigen Receptor to Patients With CD123+ AML


Clinical Trial Description

Assessment of the Safety and Feasibility of Administering T Cells Expressing an Anti-CD123 Chimeric Antigen Receptor to Patients With CD123+ AML and determine the best dosage. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03585517
Study type Interventional
Source Beijing Immunochina Medical Science & Technology Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date July 21, 2018
Completion date October 1, 2020

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