NCT04173988

A Single Center, Open Label, Single Arm Exploratory Clinical Study of CD19-Directed Allogeneic Chimeric Antigen Receptor CART-cell Immunotherapy Cell Therapy in Pediatric Patients With Relapsed/Refractory B-Cell Acute Lymphoblastic Leukemia

Study Summary

The purpose of this study is to evaluate the safety and tolerability of CD19-Directed Allogeneic Chimeric Antigen Receptor T- cell (alloCART-19)therapy in pediatric patients with relapsed/refractory acute lymphoblastic leukemia(ALL).

Want to learn more about this trial?

Request More Info

Interventions

alloCART-19GENETIC
AlloCART-19 is an allogeneic CAR-T cell product targeting CD19. * For children with body weight ≤ 50 kg, dose range for dose escalation will be 0.5 - 5 × 10\^6 CAR+ cells/kg * For children with body weight \> 50 kg, dose range for dose escalation will be 0.25 - 2.5 × 10\^8 CAR+ cells.
CyclophosphamideDRUG
Chemotherapy for lymphodepletion
FludarabineDRUG
Chemotherapy for lymphodepletion

Study Locations

FacilityCityStateCountry
Children's Hospital of Fudan UniversityShanghaiMinhangChina

Official Trial Information

View on ClinicalTrials.gov

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