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Clinical Trial Summary

The primary purpose of this study is to determine the safety and efficacy of novel autologous CAR-T cells in patients with relapsed/refractory hematological malignancies.


Clinical Trial Description

CAR-T cells targeted CD19 have demonstrated unprecedented successes. Besides CD19, many other molecules such as CD123, BCMA, and CD7 may be potential in developing the corresponding CAR-T cells to treat patients with hematopoietic and lymphoid malignancies. UTC Therapeutics Inc. have developed an efficient platform for constructing CAR-T cells that can remodel of tumor microenvironment and enhance the anti-tumor immune response and persistence of CAR-T cells. In this study, all eligible subjects will receive a conditioning chemotherapy regimen of fludarabine and cyclophosphamide followed by investigational treatment, CAR-T cells. Safety and efficacy of the CAR-T cells will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05528887
Study type Interventional
Source The Affiliated People's Hospital of Ningbo University
Contact Ying Lu
Phone 86-13486090834
Email 814871416@qq.com
Status Recruiting
Phase Phase 1
Start date September 16, 2021
Completion date June 2026

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