drugset / Trial / NCT05023707

Summary

This is a prospective,open-label, phase1/2 study to evaluate the safety and efficacy of anti-FLT3 chimeric antigen receptor engineered T cell immunotherapy (CART) in the treatment of FLT3 positive relapsed or refractory acute myeloid leukemia.

Timeline

Start
2021-12-31
Primary completion
2023-06-30
Completion
2025-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject anti-FLT3 CAR-T Cell therapy — Intravenous