drugset / Trial / NCT01160289

A Study of LY900010 in Erectile Dysfunction

NCT01160289 ↗

Phase 2 Completed 410 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of the study is to compare the efficacy of LY2452473 + tadalafil to tadalafil alone in improving the erectile function (EF) of men with erectile dysfunction (ED) who incompletely respond to tadalafil alone.

Timeline

Start
2010-10
Primary completion
2011-11
Completion
2011-11

Outcome

Missed primary endpoint

registry analysis (superiority or other test); 1 mg LY2452473 and 5 mg Tadalafil vs 5 mg Tadalafil; p = 0.5; NCT01160289 ↗

registry analysis (superiority or other test); 5 mg LY2452473 and 5 mg Tadalafil vs 5 mg Tadalafil; p = 0.498; NCT01160289 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2452473 Small molecule 1 mg Oral
Subject LY2452473 Small molecule 5 mg Oral
Subject Tadalafil Small molecule 5 mg Oral
Subject Tadalafil Small molecule 10 mg Oral

Indications