Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Chronic Lymphoblastic Leukemia
  • Non Hodgkin's Lymphoma
  • Peripheral T Cell Lymphoma
  • Relapsed or Refractory B Cell Non-Hodgkin's Lymphoma
Type
Interventional
Phase
Early Phase 1
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Biological: Autologous ??T cells Cells will be extracted by apheresis, followed by expanding and activating. The autologous ??T cells product will be adoptive transferred.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 75 years
Gender
Both males and females

Description

This is a single-centre, non-randomised, open label, no control, prospective clinical trial. The study will include the following sequential phases: sign informed consent, ??T cells pre-culture, screening and registration to the trial, apheresis, ??T cells preparation, pre-treatment for lymphodeplet...

This is a single-centre, non-randomised, open label, no control, prospective clinical trial. The study will include the following sequential phases: sign informed consent, ??T cells pre-culture, screening and registration to the trial, apheresis, ??T cells preparation, pre-treatment for lymphodepleting chemotherapy (selectable plan), treatment and follow-up. The study will evaluate the safety and efficacy of the autologous ??T cells in patients with relapsed or refractory B cell non-Hodgkin's lymphoma (B-NHL), chronic lymphoblastic leukemia (CLL) and peripheral T cell lymphoma (PTCL) expect for ??T lymphoma.

Tracking Information

NCT #
NCT04028440
Collaborators
  • Beijing GD Initiative Cell Therapy Technology Co., Ltd.
  • Chinese Academy of Medical Sciences
Investigators
Principal Investigator: Dehui Zou, Dr. Institute of Hematology & Blood Disease Hospital