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Completed Phase 3 Interventional Results available

A Study of Degarelix in Patients With Prostate Cancer

ClinicalTrials.gov ID: NCT00928434

Public ClinicalTrials.gov record NCT00928434. 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 Sep 1, 2026, 10:08 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 Randomized, Controlled, Open-Label Study Investigating the Safety and Efficacy of Degarelix Given Intermittently vs Continuous Androgen Deprivation Therapy With Lupron or Degarelix in Patients With Prostate Cancer With Prior Treatment Failure After Localized Treatment

Brief summary

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

The purpose of this study was to see if giving Degarelix every month for 7 months then stop treatment for 7 months (intermittent therapy) would show a reduction of negative effects of androgen deprivation therapy by increasing the quality of life while keeping prostate specific antigen (PSA) levels suppressed.

Study identification

NCT ID
NCT00928434
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
409 participants

Conditions and interventions

Interventions

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
Apr 30, 2009
Primary completion
Jul 31, 2012
Completion
Jul 31, 2012
Last update posted
Dec 12, 2016

2009 – 2012

United States locations

U.S. sites
59
U.S. states
20
U.S. cities
57
Facility City State ZIP Site status
Alabama Clinical Research, Inc Alexander City Alabama
Urology Center of Alabama, PC Homewood Alabama
Advanced Urology Medical Center Anaheim California
Peninsula Urology Medical Center Atherton California
Urology Associates of Central California Fresno California
South Orange County Medical Research Center Laguna Hills California
Atlantic Urology Medical Group Long Beach California
San Bernardino Urological Associates San Bernardino California
San Diego Uro-Research San Diego California
Santa Barbara Clinical Research Santa Barbara California
University of Colorado Health Sciences Center Aurora Colorado
The Urology Center of Colorado Denver Colorado
Urology Associates Research Englewood Colorado
Connecticut Clinical Research Center Middlebury Connecticut
Grove Hill Medical Center New Britain Connecticut
Walter Reed Army Hospital Medical Center Washington D.C. District of Columbia
South Florida Medical Research Aventura Florida
Urology Health Solutions, Inc Celebration Florida
Florida Urology Physicians Fort Myers Florida
University of Florida Gainesville Florida
Winter Park Urology Associates Orlando Florida
Southeastern Urology Center, PA Tallahassee Florida
Tampa Bay Urology Tampa Florida
Advanced Research Institute, Inc Trinity Florida
Urology Enterprises Marietta Georgia
Midwest Urology/RMD Clinical Research Institute Melrose Park Illinois
Deaconess Clinic Inc Evansville Indiana
Northeast Indiana Research Fort Wayne Indiana
Metropolitan Urology, PSC Jeffersonville Indiana
Regional Urology, Lic Shreveport Louisiana
Chesapeake Urology Associates Baltimore Maryland
Chesapeake Urology Research Associates Baltimore Maryland
Chesapeake Urology Research Associates Glen Burnie Maryland
Myron Murdock M.D. LLC Greenbelt Maryland
Chesapeake Urology Associates, PA Towson Maryland
Urology Associates of Englewood Englewood New Jersey
Hamilton Urology PA Hamilton New Jersey
Lawrenceville Urology Lawrenceville New Jersey
Nationsmed Clinical Research Perth Amboy New Jersey
Center for Urologic Care Voorhees Township New Jersey
Delaware Valley Urology LLC Woodlane New Jersey
The Urological Institute of NE NY, CCP Albany New York
Medical & Clinical Research Associates Bay Shore New York
Brooklyn Heights Urology Associates, P.C. Brooklyn New York
University Urology Associates New York New York
Hudson Valley Urology P.C. Poughkeepsie New York
Northeast Urology Research Concord North Carolina
Alliance Urology Specialists Greensboro North Carolina
Urological Association of Lancaster Lancaster Pennsylvania
State College Urologic Association State College Pennsylvania
Carolina Urologic Research Center Myrtle Beach South Carolina
Lexington Urological Associates, PA West Columbia South Carolina
Urology Associates Nashville Tennessee
Lackland Air Force base San Antonio Texas
Urology of Virginia Norfolk Virginia
Virginal Urology Richmond Virginia
Virginia Urology Center Richmond Virginia
Seattle Urology Research Center Seattle Washington
Roger D. Fincher, PS Spokane Washington

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 NCT00928434, 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 Dec 12, 2016 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00928434 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →