drugset / Trial / NCT01577680

A Study to Assess the Effects of GSK573719/VI Combination and GSK573719 Monotherapy in Subjects With Moderate Hepatic Impairment and Matched Healthy Volunteers

NCT01577680

Phase 1 Completed 18 enrolled GlaxoSmithKline
Non-randomizedCrossoverOpen-labelBasic science

Summary

This study will assess the safety and pharmacokinetics of GSK573719 and GSK573719/vilanterol combination in healthy subjects and subjects with moderate hepatic impairment. The results of this study will provide guidance on the use of the product in patients with hepatic impairment.

Timeline

Start
2012-03-05
Primary completion
2012-06-29
Completion
2012-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Umeclidinium Other / unclassified 125 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug