drugset / Trial / NCT00769041

A Thorough EKG Safety Study of TA-1790 (Avanafil)

NCT00769041

Phase 1 Completed 57 enrolled VIVUS LLC Covance · collab
RandomizedCrossoverDouble-blindTreatment

Summary

This study is to assess whether treatment with a therapeutic (100 mg) or supratherapeutic (800 mg) dose of avanafil has the potential to cause QT/QTc prolongation in healthy volunteers.

Timeline

Start
2008-10
Primary completion
2009-01
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Avanafil Small molecule 100 mg
Subject Avanafil Small molecule 800 mg
Comparator Moxifloxacin Small molecule 400 mg

Indications