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Subcutaneous Testosterone Replacement Efficacy and Safety in Adult Men Diagnosed With Hypogonadism — STEADY  

Hypogonadism Clinical Trial

Official title:
A Multiple-dose, 52-week Study to Evaluate the Efficacy and Safety of Testosterone Enanthate Administered Subcutaneously Once Each Week to Adult Males With Hypogonadism

Clinical Trial Summary

Evaluation of efficacy and safety of testosterone enanthate administered subcutaneously using an auto-injector

Clinical Trial Description

This study will evaluate, if testosterone enanthate administered subcutaneously once each week by an auto-injector to men with low testosterone, can raise their levels into the normal range.

The study will investigate the ability to adjust testosterone enanthate dose levels using single point blood concentrations.

Safety and tolerability of testosterone administration will be evaluated along with the patient's ability to use the auto-injector and follow the instructions for auto-injector use. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02159469
Study type Interventional
Source Antares Pharma Inc.
Contact
Status Completed
Phase Phase 3
Start date July 2014
Completion date November 2015
View Details
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