drugset / Trial / NCT01054261

To Compare the Pharmacokinetics of Avanafil in Subjects With Mild and Moderate Renal Impairment to Subjects With Normal Renal Function.

NCT01054261

Phase 1 Completed 24 enrolled VIVUS LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to compare the pharmacokinetics of avanafil in subjects with mild and moderate renal impairment and to assess the safety and toleration of avanafil in subjects with mild and moderate renal impairment.

Timeline

Start
2010-01
Primary completion
2010-02
Completion
2010-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Avanafil Small molecule 200 mg

Indications

No indication recorded.