CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,717 enrolled
Drug / intervention
Enzalutamide +1 moredrug
Likely dose
Enzalutamide 160 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01212991
NCT01212991Phase 3Completed

PREVAIL: A MULTINATIONAL PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED EFFICACY AND SAFETY STUDY OF ORAL MDV3100 IN CHEMOTHERAPY-NAÏVE PATIENTS WITH PROGRESSIVE METASTATIC PROSTATE CANCER WHO HAVE FAILED ANDROGEN DEPRIVATION THERAPY

Pfizer·interventional·Posted Oct 1, 2010·Updated Mar 17, 2020

In Brief

A Phase 3 clinical trial evaluating Enzalutamide and Placebo for Prostate Cancer. Completed, enrolled 1,717 participants across 269 sites in 22 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProstate Cancer
CountriesAustralia, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Israel, Italy, Japan, Lithuania, Netherlands, Poland, Russia, Singapore, Slovakia, South Korea, Spain, Sweden, United Kingdom, United States

Timeline

Phase 3CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedOct 1, 2010
Enrollment StartSep 16, 2010
Primary CompletionSep 30, 2013
Study CompletionFeb 14, 2019
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 15.8 years ago

Interventions

Enzalutamidedrug

Participants received enzalutamide 160 mg, administered as four 40-mg capsules, once per day by mouth. Study drug treatment continued until disease progression (evidence of radiographic progression, a skeletal-related event, or clinical progression) and the initiation of a cytotoxic chemotherapy or an investigational agent, unacceptable toxicity, or withdrawal.

Placebodrug

Participants received placebo, administered as four capsules, once per day by mouth. Study drug treatment continued until disease progression (evidence of radiographic progression, a skeletal-related event, or clinical progression) and the initiation of a cytotoxic chemotherapy or an investigational agent, unacceptable toxicity, or withdrawal.