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

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Last updated:1st Jul 2014

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

Study Type: Interventional
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Double-blind, Multiple-dose, 52-week Study to Evaluate the Efficacy and Safety of Testosterone Enanthate Administered Subcutaneously Once Each Week to Adult Males With Hypogonadism
Enrollment: 150
Study Start Date: July 2014
Study Completion Date: November 2015
Primary Completion Date: February 2015 (Final data collection date for primary outcome measure)

- Experimental:
Testosterone enanthate auto-injector

Category Value
Study start date 2014-07-01

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