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Completed No phase listed Observational

Real-World Study of Enzalutamide and Abiraterone Acetate (With Prednisone) Tolerability

ClinicalTrials.gov ID: NCT02663193

Public ClinicalTrials.gov record NCT02663193. 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 May 7, 2026, 1:18 PM 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 Multicenter, Two-arm, Prospective, Observational Study to Characterize the Tolerability of Treatment With Enzalutamide or Abiraterone Acetate (With Prednisone) for Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Study identification

NCT ID
NCT02663193
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Janssen Scientific Affairs, LLC
Industry
Enrollment
108 participants

Conditions and interventions

Interventions

  • No Intervention Other

Other

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
Nov 30, 2015
Primary completion
Dec 31, 2016
Completion
Dec 31, 2016
Last update posted
Feb 2, 2025

2015 – 2017

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Not listed Homewood Alabama
Not listed La Mesa California
Not listed Wheat Ridge Colorado
Not listed Daytona Beach Florida
Not listed Indianapolis Indiana
Not listed Jeffersonville Indiana
Not listed Saint Clair Shores Michigan
Not listed Englewood New Jersey
Not listed Lawrenceville New Jersey
Not listed Morristown New Jersey
Not listed Poughkeepsie New York
Not listed Syracuse New York
Not listed Middleburg Heights Ohio
Not listed Springfield Oregon
Not listed Bala-Cynwyd Pennsylvania
Not listed Lancaster Pennsylvania
Not listed Charleston South Carolina
Not listed Myrtle Beach South Carolina
Not listed San Antonio Texas
Not listed Virginia Beach Virginia

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02663193, 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 Feb 2, 2025 · Synced May 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02663193 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →