NCT05528887

Safety and Efficacy Study of Chimeric Antigen Receptor T (CAR-T) Cells in the Treatment of Relapsed/Refractory Hematological Malignancies

Study 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.

Want to learn more about this trial?

Request More Info

Interventions

Autologous CAR-T cellsBIOLOGICAL
D0: CAR-T cells will be infused intravenously.
FludarabineDRUG
D-5 to D-3: Fludarabine (30 mg/m\^2/day) will be administered intravenously for 3 days.
CyclophosphamideDRUG
D-5 to D-3: Cyclophosphamide (500 mg/m\^2/day) will be administered intravenously for 3 days.

Study Locations

FacilityCityStateCountry
The Affiliated People's Hospital of Ningbo UniversityNingboZhejiangChina

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026