drugset / Trial / NCT02446405

Enzalutamide in First Line Androgen Deprivation Therapy for Metastatic Prostate Cancer

NCT02446405 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the effectiveness of enzalutamide, versus a conventional non-steroidal anti androgen (NSAA), when combined with a luteinizing hormone releasing hormone analog (LHRHA) or surgical castration, as first line androgen deprivation therapy (ADT) for newly diagnosed metastatic prostate cancer.

Timeline

Start
2014-03
Primary completion
2026-12-31
Completion
2027-06-30

Outcome

Met primary endpoint

paper There were 102 deaths in the enzalutamide group and 143 deaths in the standard-care group PMID 31157964 ↗

paper hazard ratio, 0.67; 95% confidence interval [CI], 0.52 to 0.86; P = 0.002 PMID 31157964 ↗

paper overall survival at 3 years were 80% (based on 94 events) in the enzalutamide group and 72% (based on 130 events) in the standard-care group. PMID 31157964 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bicalutamide Other / unclassified — Oral
Subject Enzalutamide Other / unclassified 160 mg Oral
Comparator Flutamide Small molecule — Oral
Comparator Nilutamide Small molecule — Oral

Indications