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Terminated Phase 2 Interventional Results available

Phase II, Dose Finding Study of GTx-758

ClinicalTrials.gov ID: NCT01393119

Public ClinicalTrials.gov record NCT01393119. 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 6, 2026, 10:00 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

Phase II, Open-label, Loading and Maintenance Dose Finding Study of GTx-758 in Men With Prostate Cancer

Brief summary

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

The purpose of this study is to determine the appropriate loading and maintenance dose of GTx-758 to reach and maintain castration for the duration of the study.

Study identification

NCT ID
NCT01393119
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
GTx
Industry
Enrollment
77 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
45 Years to 80 Years
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
Jul 31, 2011
Primary completion
Nov 30, 2012
Completion
Nov 30, 2012
Last update posted
Apr 21, 2024

2011 – 2012

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
GTx Investigative Site Glendale Arizona 85306
GTx Investigative Site Phoenix Arizona 85032
GTx Investigative Site La Mesa California 91942
GTx Investigative Site San Bernardino California 92404
GTx Investigative Site Aventura Florida 33180
GTx Investigative Site Bradenton Florida 34205
GTx Investigative Site St. Petersburg Florida 33710
GTx Investigative Site Tampa Florida 33607
GTx Investigative Site Roswell Georgia 30076
GTx Investigative Site Jeffersonville Indiana 47130
GTx Investigative Site Shreveport Louisiana 71106
GTx Investigative Site Annapolis Maryland 21401
GTx Investigative Site Towson Maryland 21204
GTx Investigative Site Hamilton New Jersey 08690
GTx Investigative Site Albany New York 12208
GTx Investigative Site Oneida New York 13421
GTx Investigative Site Syracuse New York 13210
GTx Investigative Site Concord North Carolina 28025
GTx Investigative Site Cincinnati Ohio 45212
GTx Investigative Site Columbus Ohio 43220
GTx Investigative Site Bala-Cynwyd Pennsylvania 19004

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 NCT01393119, 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 Apr 21, 2024 · Synced Sep 6, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01393119 live on ClinicalTrials.gov.

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