drugset / Trial / NCT01017952

A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

NCT01017952

Phase 3 Completed 1635 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

The Purpose of this study is to assess the efficacy and safety of three strengths of the FF/GW642444 Inhalation Powder in subject with Chronic Obstructive Pulmonary Disease (COPD)

Timeline

Start
2009-09-25
Primary completion
2011-10-01
Completion
2011-10-17

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone Furoate Other / unclassified 50 ug Inhaled
Subject Fluticasone Furoate Other / unclassified 100 ug Inhaled
Subject Fluticasone Furoate Other / unclassified 200 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug Inhaled