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Assessment of Long Term Treatment With Testosterone Undecanoate in Males With Hypogonadism

Hypogonadism Clinical Trial

Official title:
Open One-arm Study to Investigate Safety and Efficacy of Intramuscular Injections of 1000 mg Testosterone Undecanoate (TU) in Hypogonadal Men at Variable Intervals During a 136-week to 192-week Treatment Including Pharmacokinetics

Clinical Trial Summary

This study will evaluate the preparation of testosterone undecanoate under conditions which resemble real-life situations.

Clinical Trial Description

The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer Schering Pharma AG, Germany.Bayer Schering Pharma AG, Germany is the sponsor of the trial. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00220298
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date February 2003
Completion date October 2007
View Details
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