ClinicalTrials.gov record
Completed Phase 1 Interventional

Study of Relugolix in Men With Metastatic Castration-Sensitive Prostate Cancer or Non-Metastatic or Metastatic Castration-Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT04666129

Public ClinicalTrials.gov record NCT04666129. 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 20, 2026, 7:02 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 Phase 1, Three-Part, Open-Label, Parallel-Cohort Safety and Tolerability Study of Relugolix in Combination With Abiraterone Acetate Plus a Corticosteroid, Apalutamide, or Docetaxel With or Without Prednisone in Men With Metastatic Castration-Sensitive Prostate Cancer or Non-Metastatic or Metastatic Castration-Resistant Prostate Cancer

Study identification

NCT ID
NCT04666129
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
48 participants

Conditions and interventions

Interventions

  • Abiraterone Drug
  • Apalutamide Drug
  • Docetaxel Drug
  • Methylprednisolone Drug
  • Prednisone Drug
  • Relugolix Drug

Drug

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
Feb 17, 2021
Primary completion
May 27, 2024
Completion
May 27, 2024
Last update posted
Aug 16, 2025

2021 – 2024

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Urological Associates of Southern Arizona, P.C. Tucson Arizona 85741
Arkansas Urology Little Rock Arkansas 72211
Colorodo Clinical Research Lakewood Colorado 80228
Chesapeake Urology Research Associates Baltimore Maryland 21204
University of Massachusetts Medical School Worcester Massachusetts 01655
New Jersey Urology Saddle Brook New Jersey 07663
Clinical Research Alliance, Inc. Westbury New York 11590
Alliance Urology Greensboro North Carolina 27403
Wake Forest Baptist Health Winston-Salem North Carolina 27157
Helios Clinical Research, LLC. Middleburg Heights Ohio 44130
Center for Advanced Urology, LLP d/b/a: MidLantic Urology Bala-Cynwyd Pennsylvania 19004
Keystone Urology Specialists Lancaster Pennsylvania 17604
Carolina Urologic Research Center Myrtle Beach South Carolina 29572
Urology Associates, P.C. Nashville Tennessee 37209
UT Southwestern Medical Center Dallas Texas 75390
Urology San Antonio San Antonio Texas 78229

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 NCT04666129, 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 Aug 16, 2025 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04666129 live on ClinicalTrials.gov.

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