drugset / Trial / NCT07567521
A Study of TRC003 in the Treatment of Patients With Progressive PSMA-positive mCRPC
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TRC003 | Other / unclassified | 7.4 mbq | Intravenous |
| Subject | TRC003 | Other / unclassified | 9.25 mbq | Intravenous |
| Subject | TRC003 | Other / unclassified | 11.1 mbq | Intravenous |