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

PHASE1RecruitingINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

March 27, 2025

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions
Metastatic Prostate CancerCastration-resistant Prostate CancerMetastatic Castration-resistant Prostate Cancer
Interventions
BIOLOGICAL

PSMA-UCAR T (BRL-302)

"Three patients will be firstly enrolled at a dose level (DL) of 5.0 × 10\^6cells/kg in the DL1 group, following lymphodepleting chemotherapy which will be given under instruction of protocol and investigators' assessment;~Based on preliminary safety data, efficacy information, and PK/PD parameters obtained at DL1 cohort, the investigator may enroll another three patients in a decreased dose level group of DL-2: 3 × 10\^6 cells/kg or DL-1:1 × 10\^6 cells/ kg, after thorough discussions between the investigators."

Trial Locations (1)

201109

RECRUITING

Changzheng hospital, Shanghai

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bioray Laboratories

INDUSTRY

lead

Shanghai Changzheng Hospital

OTHER

NCT06895811 - Clinical Study of Safety and Efficacy of Universal PSMA CAR- T in Refractory CRPC | Biotech Hunter | Biotech Hunter