drugset / Trial / NCT04015622

PROstate Cancer TReatment Optimization Via Analysis of Circulating Tumour DNA

NCT04015622

Phase 2 Active not recruiting 100 enrolled British Columbia Cancer Agency
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to assess the strategy in treatment selection using ctDNA fraction as a predictive biomarker to direct treatment decision (ctDNA fraction \<2% receives enzalutamide, and ctDNA fraction ≥2% receives docetaxel) versus clinician's choice of enzalutamide or docetaxel, in subjects with metastatic castration-resistant prostate cancer post abiraterone setting.

Timeline

Start
2020-10-07
Primary completion
2026-04-01
Completion
2026-12-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 75 mg/m2 Intravenous
Subject Enzalutamide Other / unclassified 160 mg Oral