drugset / Trial / NCT01067365

Study to Evaluate the Safety and Efficacy of Androxal Treatment in Men With Secondary Hypogonadism

NCT01067365

Phase 3 Completed 104 enrolled Repros Therapeutics Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Subjects who completed ZA-003 were eligible to receive an additional year of treatment in this extension study.

Timeline

Start
2006-03
Primary completion
2007-05
Completion
2007-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Androxal Unknown 12.5 mg Oral
Subject Androxal Unknown 25 mg Oral

Indications