Testosterone Replacement in Men With Non-Metastatic Castrate Resistant Prostate Cancer

NCT00515112 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2014-06-11

Study results available
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Summary

The purpose of this study is to determine whether prostate cancer growth can be slowed in patients who receive Androgel® 1% at 10 gram dose.

Conditions

Interventions

DRUG

AndroGel

Androgel 1%, 10g daily

DRUG

placebo

placebo

Sponsors & Collaborators

  • Solvay Pharmaceuticals

    collaborator INDUSTRY
  • University of Chicago

    lead OTHER

Principal Investigators

  • Walter Stadler, MD · University of Chicago

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2010-11-30
Completion
2012-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00515112 on ClinicalTrials.gov