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Clinical Trial Summary

To evaluate the safety and efficacy of Dasatinib plus CD19/CD22 Bispecific CAR-T for the treatment of elderly Ph-positive lymphoblastic leukemia. Newly diagnosed Ph-positive patients will be given Dasatinib plus VP chemotherapy for induction treatment,if a hematologic complete remission was observed then a lymphocyte collection will be administrated to patients. Then chemotherapy regimen of fludarabine and cyclophosphamide followed by a single infusion of CD19/CD22 CAR+ T cells


Clinical Trial Description

Newly diagnosed ph-positive ALL patients over 60 and less than 70 years old will be enrolled. Patients will be given Dasatinib plus VP chemotherapy for induction remission treatment, if a hematologic complete remission was observed then a lymphocyte collection will be administrated to patients. Then chemotherapy regimen of fludarabine and cyclophosphamide followed by a single infusion of CD19/CD22 CAR+ T cells ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05523661
Study type Interventional
Source Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Contact Xianmin Song, M.D.
Phone 021-63240090
Email shongxm@139.com
Status Recruiting
Phase Phase 1
Start date March 1, 2021
Completion date September 1, 2025

See also
  Status Clinical Trial Phase
Terminated NCT04115059 - Dasatinib In Waldenström Macroglobulinemia Phase 1
Recruiting NCT04155411 - Dose Reduced Dasatinib (70 mg Daily) as First-line Treatment for Newly Diagnosed CML-CP Phase 4