drugset / Trial / NCT06228404

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

NCT06228404 ↗

Phase 0 Active not recruiting 18 enrolled Shanghai Changzheng Hospital Bioray Laboratories · collab
NaSequentialOpen-labelTreatment

Summary

This is one center, single-arm, open-label investigator initiated trial to assess the safety and efficacy of enhanced autologous PSMA chimeric antigen receptor T cells in the treatment for patients with refractory castration resistant prostate cancer, and the sample size is set to 7-18 subjects.

Timeline

Start
2024-03-03
Primary completion
2026-05
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Enhanced autologous PSMA-CAR T Unknown 250000 cells/kg —
Subject Enhanced autologous PSMA-CAR T Unknown 750000 cells/kg —
Subject Enhanced autologous PSMA-CAR T Unknown 2e+06 cells/kg —