drugset / Trial / NCT01212991

A Safety and Efficacy Study of Oral MDV3100 in Chemotherapy-Naive Patients With Progressive Metastatic Prostate Cancer

NCT01212991 ↗

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine the benefit of enzalutamide versus placebo as assessed by overall survival and progression-free survival in patients with progressive metastatic prostate cancer who have failed androgen deprivation therapy but not yet received chemotherapy.

Timeline

Start
2010-09-16
Primary completion
2013-09-30
Completion
2019-02-14

Outcome

Met primary endpoint

registry Enzalutamide vs Placebo; p <0.0001; Hazard Ratio (HR) 0.706 (95% CI 0.596 to 0.837) NCT01212991 ↗

registry Enzalutamide vs Placebo; p <0.0001; Hazard Ratio (HR) 0.186 (95% CI 0.149 to 0.231) NCT01212991 ↗

release “The Phase 3 PREVAIL Trial of Enzalutamide Meets Both Co-Primary Endpoints of Overall Survival and Radiographic Progression-Free Survival” astellas.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enzalutamide Other / unclassified 160 mg Oral

Indications