drugset / Trial / NCT06895811

Clinical Study of Safety and Efficacy of Universal PSMA CAR- T in Refractory CRPC

NCT06895811 ↗

Phase 1 Active not recruiting 3 enrolled Shanghai Changzheng Hospital Bioray Laboratories · collab
NaSingle-groupOpen-labelTreatment

Summary

This is a single-arm, single-center, open-label clinical trial designed to evaluate the clinical safety and tolerability of different doses of Prostate-Specific Membrane Antigen (PSMA)-Universal Chimeric Antigen Receptor (UCAR) T-lymphocytes (PSMA-UCAR T) for the treatment of patients with refractory castration-resistant prostate cancer (CRPC).

Timeline

Start
2025-03-27
Primary completion
2026-07
Completion
2026-11

Drugs

EvaluationDrugModalityDoseRoute
Subject PSMA-UCAR T Cell therapy 1 cells/kg —
Subject PSMA-UCAR T Cell therapy 3 cells/kg —
Subject PSMA-UCAR T Cell therapy 5 cells/kg —