drugset / Trial / NCT00415571

Efficacy and Safety Evaluating Fispemifene in the Treatment of Hypogonadal Men With Erectile Dysfunction Unresponsive to PDE5 Inhibitors

NCT00415571 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of the study is to assess and compare the preliminary efficacy, safety and tolerability of fispemifene 300 mg and placebo given once daily for 8 weeks in the treatment of hypogonadal men with erectile dysfunction (ED) unresponsive to PDE5 inhibitors.

Timeline

Start
2006-12
Primary completion
—
Completion
2008-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fispemifene Small molecule 300 mg —