drugset / Trial / NCT06150885

A Safety and Efficacy Study of Allogeneic CAR Gamma-Delta T Cells in Subjects with Relapsed/Refractory Solid Tumors

NCT06150885 ↗

Phase 1/2 Recruiting 60 enrolled Ever Supreme Bio Technology Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This study is composed of phase I and IIa parts. The dose-escalation phase I part aims to find the maximum tolerated dose (MTD) and to identify the safety of CAR001 in subjects with relapsed/refractory solid tumor; the dose-expansion phase IIa part aims to evaluate the potential efficacy of CAR001 in subjects with relapsed/refractory non-small cell lung cancer (NSCLC), triple negative breast cancer (TNBC), colorectal cancer (CRC) or Glioblastoma multiforme (GBM).

Timeline

Start
2024-09-01
Primary completion
2027-06-30
Completion
2027-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HLA-G-CAR.BiTE allogeneic γδ T cells Cell therapy — Intravenous

Indications