drugset / Trial / NCT07567521

A Study of TRC003 in the Treatment of Patients With Progressive PSMA-positive mCRPC

NCT07567521 ↗

Phase 1/2 Recruiting 90 enrolled C Ray Therapeutics
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate safety and tolerability, pharmacokinetics (PK), efficacy of TRC003 injection in patients with progressive PSMA-positive mCRPC who have been treated with androgen receptor pathway inhibitor (ARPI) or taxane-based chemotherapy. We plan to recruit 90 participants who will be randomly assigned to 1 of 3 dose cohorts (30 cases per dose cohort) with up to 6 cycles of treatment in this study.

Timeline

Start
2026-05-22
Primary completion
2027-12-30
Completion
2029-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject TRC003 Other / unclassified 7.4 mbq Intravenous
Subject TRC003 Other / unclassified 9.25 mbq Intravenous
Subject TRC003 Other / unclassified 11.1 mbq Intravenous

Indications