drugset / Trial / NCT06520345

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

NCT06520345

Phase 3 Recruiting 520 enrolled Telix Pharmaceuticals (Innovations) Pty Limited
RandomizedParallel-groupOpen-labelTreatment

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

Timeline

Start
2024-07-26
Primary completion
2027-12
Completion
2030-12

Drugs

EvaluationDrugModalityDoseRoute
Subject 177Lu-TLX591 Unknown 2812 mbq
Background Abiraterone acetate Small molecule 1000 mg
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Enzalutamide Other / unclassified 160 mg

Indications