drugset / Trial / NCT02677896

A Study of Enzalutamide Plus Androgen Deprivation Therapy (ADT) Versus Placebo Plus ADT in Patients With Metastatic Hormone Sensitive Prostate Cancer (mHSPC)

NCT02677896 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to evaluate the efficacy of enzalutamide plus androgen deprivation therapy (ADT) as measured by radiographic progression-free survival (rPFS) based on central review. The study also evaluated the safety of enzalutamide plus ADT in mHSPC.

Timeline

Start
2016-03-09
Primary completion
2018-10-14
Completion
2024-07-31

Outcome

Met primary endpoint

registry Enzalutamide + Androgen Deprivation Therapy (ADT) vs Placebo + Androgen Deprivation Therapy (ADT); p <0.0001; Cox hazard ratio 0.39 (95% CI 0.30 to 0.50) NCT02677896 ↗

paper risk of radiographic progression or death was significantly reduced with enzalutamide plus ADT versus placebo plus ADT PMID 31329516 ↗

release “Phase 3 ARCHES trial evaluating XTANDI® (enzalutamide) plus androgen deprivation therapy (ADT) in men with metastatic hormone-sensitive prostate cancer (mHSPC) met its primary endpoint” astellas.com ↗

release “Phase 3 ARCHES Trial Shows XTANDI® (enzalutamide) Significantly Improved Radiographic Progression-Free Survival in Men with Metastatic Hormone-Sensitive Prostate Cancer” astellas.com ↗

release “ARCHES, a randomized Phase 3 study which evaluated 1,150 men with mCSPC and met its primary endpoint” pfizer.com ↗

release “The primary results from the ARCHES trial were published in the Journal of Clinical Oncology in 2019. The study met its primary endpoint” astellas.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enzalutamide Other / unclassified 160 mg Oral