Overview

The Study of 177Lu-TLX591 Plus SOC Versus SOC Alone in Patients With mCRPC (ProstACT Global)

Status:
RECRUITING
Trial end date:
2030-12-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to evaluate the efficacy and safety of 177Lu-TLX591 in patients with metastatic castration-resistant prostate cancer who have progressed following treatment with Androgen Receptor Pathway Inhibitor Treatment
Phase:
PHASE3
Details
Lead Sponsor:
Telix Pharmaceuticals (Innovations) Pty Limited
Treatments:
abiraterone
Docetaxel
enzalutamide
Lutetium
Lutetium-177