drugset / Trial / NCT07556757

A Safety and Efficacy Study of CD-19 t-haNK in Patients With B-cell Acute Lymphoblastic Leukemia

NCT07556757

Phase 1 Recruiting 10 enrolled ImmunityBio, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1, open-label study to evaluate the safety and efficacy of CD19 t-haNK in patients with B-cell acute lymphoblastic leukemia. Up to 10 patients will receive at least 1 dose of study drug.

Timeline

Start
2025-04-11
Primary completion
2028-12
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject CD19 t-haNK Cell therapy Intravenous

Indications