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Completed Phase 2 Interventional Results available

Study of the Effect of GTx-758 on Serum PSA and Testosterone in Men With Prostate Cancer

ClinicalTrials.gov ID: NCT01615120

Public ClinicalTrials.gov record NCT01615120. 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 Jul 21, 2026, 6:06 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

Phase II, Open Label Study of the Effect of GTx-758 as Secondary Hormonal Therapy on Serum PSA and Serum Free Testosterone Levels in Men With Metastatic Castration Resistant Prostate Cancer Maintained on Androgen Deprivation Therapy

Study identification

NCT ID
NCT01615120
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GTx
Industry
Enrollment
77 participants

Conditions and interventions

Interventions

  • GTx-758 125 mg Drug
  • GTx-758 250 mg 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
Aug 13, 2012
Primary completion
Nov 8, 2016
Completion
Nov 8, 2016
Last update posted
Mar 23, 2021

2012 – 2016

United States locations

U.S. sites
26
U.S. states
14
U.S. cities
24
Facility City State ZIP Site status
Urology Associates Medical Group Burbank California 91505
VA of Greater Los Angeles Los Angeles California 90073
Tower Urology Los Angeles California 90078
San Bernardino Urological Assoc. San Bernardino California 92404
Genesis Healthcare Partners San Diego California 92123
Urology Specialists of So. California Torrance California 90505
Univ. of Colorado Cancer Center Aurora Colorado 80045
Connecticut Clinical Research Center Middlebury Connecticut 06762
So. Florida Medical Research Aventura Florida 33180
AMPM Research Miami Florida 33145
Coastal Medical Center Sarasota Florida 34237
GTx Investigative Site St. Petersburg Florida 33710
Pinellas Urology St. Petersburg Florida 33710
Urology of Indiana Greenwood Indiana 46143
First Urology PSC Jeffersonville Indiana 47130
Chesapeake Urology Research Assoc. Towson Maryland 21204
Five Valleys Urology Missoula Montana 59808
Urological Institute of NE New York Albany New York 12208
AMP of NY Oneida New York 13421
AMP of NY Syracuse New York 13210
Carolina Clinical Trials Concord North Carolina 28025
The Urology Group Cincinnati Ohio 45212
UCSEPA Bala-Cynwyd Pennsylvania 19004
West Clinic Memphis Tennessee 38119
Urology of Virginia Virginia Beach Virginia 23462
Seattle Cancer Care Alliance, Univ. of Washington Seattle Washington 98195

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 NCT01615120, 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 Mar 23, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01615120 live on ClinicalTrials.gov.

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