drugset / Trial / NCT02164539

Evaluation of Umeclidinium Bromide in Combination With Fluticasone Furoate in COPD Subjects With an Asthmatic Component

NCT02164539

Phase 2 Completed 338 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the dose-response of 4 doses of umeclidinium bromide in combination with fluticasone furoate compared with fluticasone furoate monotherapy in chronic obstructive pulmonary disease participants with an asthmatic component. The fluticasone furoate/umeclidinium bromide treatments will also be compared to the once-daily inhaled corticosteroid/long-acting beta agonist combination fluticasone furoate/vilanterol.

Timeline

Start
2014-07-01
Primary completion
2015-07-01
Completion
2015-07-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone Furoate Other / unclassified 100 ug Inhaled
Subject Umeclidinium Other / unclassified 15.6 ug Inhaled
Subject Umeclidinium Other / unclassified 62.5 ug Inhaled
Subject Umeclidinium Other / unclassified 125 ug Inhaled
Subject Umeclidinium Other / unclassified 250 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug Inhaled