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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT02677896

Public ClinicalTrials.gov record NCT02677896. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 1:39 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multinational, Phase 3, Randomized, Double-blind, Placebo-controlled Efficacy and Safety Study of Enzalutamide Plus Androgen Deprivation Therapy (ADT) Versus Placebo Plus ADT in Patients With Metastatic Hormone Sensitive Prostate Cancer (mHSPC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02677896
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
1,150 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 9, 2016 (Actual)
Primary completion
Oct 14, 2018 (Actual)
Completion
Jul 31, 2024 (Actual)
Last update posted
Oct 24, 2025

2016 – 2024

United States locations

U.S. sites
34
U.S. states
23
U.S. cities
33
Facility City State ZIP Site status
Site US10016 Homewood Alabama 35209 —
Site US10007 Anchorage Alaska 99503 —
Site US10008 Tucson Arizona 85741 —
Site US10034 Fountain Valley California 92708 —
Site US10056 La Jolla California 92093 —
Site US10026 Santa Rosa California 95403 —
Site US10035 Aurora Colorado 80045 —
Site US10050 Denver Colorado 80220 —
Site US10048 St. Petersburg Florida 33710 —
Site US10054 Thomasville Georgia 31792 —
Site US10015 Chicago Illinois 60637 —
Site US10043 Springfield Illinois 62703 —
Site US10045 Jeffersonville Indiana 47130 —
Site US10020 West Des Moines Iowa 50266 —
Site US10055 Kansas City Kansas 66160-7233 —
Site US10017 Towson Maryland 21204 —
Site US10036 Omaha Nebraska 68114 —
Site US10018 Lawrenceville New Jersey 08648 —
Site US10025 Newburgh New York 12550 —
Site US10029 Syracuse New York 13210 —
Site US10068 Charlotte North Carolina 28207 —
Site US10009 Concord North Carolina 28025 —
Site US10014 Durham North Carolina 27710 —
Site US10060 Greenville North Carolina 27834 —
Site US10044 Middleburg Heights Ohio 44130 —
Site US10011 Lancaster Pennsylvania 17604 —
Site US10012 Myrtle Beach South Carolina 29572 —
Site US10059 Nashville Tennessee 37208 —
Site US10046 Dallas Texas 75231 —
Site US10004 Dallas Texas 75390-9110 —
Site US10040 Virginia Beach Virginia 23462 —
Site US10002 Burien Washington 98166 —
Site US10013 Seattle Washington 98101 —
Site US10028 Wenatchee Washington 98801 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 169 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02677896, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 24, 2025 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02677896 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →