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Clinical Trial Summary

It is a single-center, single-arm, open-labeled clinical trial to evaluate the efficacy and safety of CAR-T cells therapy for Chronic or Refractory Primary Immune Thrombocytopenia (ITP).


Clinical Trial Description

This open label and single-arm study aims to evaluate the efficacy and safety of CAR-T cells therapy in patients with Chronic or Refractory Primary Immune Thrombocytopenia (ITP). After enrollment, a leukapheresis procedure will be performed to manufacture chimeric antigen receptor (CAR) modified T cells. Patients will get a 3-5 days lymphodepletion therapy with fludarabine and cyclophosphamide, then the CAR-T cells will be infused by vein. After infusion, subjects will be followed for safety and efficacy evaluation up to 12 weeks. For those with a durable remission 12 weeks after infusion, the follow-up will last for at least 12 months for disease control. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06352281
Study type Interventional
Source 920th Hospital of Joint Logistics Support Force of People's Liberation Army of China
Contact Wang Sanbin, Doctor
Phone 13187424131
Email sanbin1011@163.com
Status Recruiting
Phase Phase 1/Phase 2
Start date February 1, 2024
Completion date December 31, 2027