drugset / Trial / NCT01706198

An Effectiveness Study Comparing Fluticasone Furoate (FF, GW685698)/Vilanterol (VI, GW642444) With Standard Treatment in Asthma

NCT01706198 ↗

Phase 3 Completed 4233 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is designed to compare the effectiveness and safety of Fluticasone Furoate/Vilanterol Inhalation Powder (100mcg Fluticasone Furoate ((FF), GW685698)/25mcg Vilanterol ((VI), GW642444) or 200mcg Fluticasone Furoate ((FF), GW685698)/25mcg Vilanterol ((VI), GW642444) ) delivered once daily via a Novel Dry Powder Inhaler (NDPI) compared with the existing asthma maintenance therapy over twelve months in subjects diagnosed with asthma. This is a Phase III multi-centre, randomised open label study. Subjects who meet the eligibility criteria are randomised and will enter a 12 month treatment period.

Timeline

Start
2012-11-01
Primary completion
2016-12-01
Completion
2016-12-16

Outcome

Met primary endpoint

paper 977 [71%] of 1373 in the fluticasone furoate and vilanterol group vs 784 [56%] of 1399 in the usual care group PMID 28903864 ↗

registry analysis (other test); Usual Care vs FF/VI; p <0.001; Adjusted Odds Ratio 2.00 (95% CI 1.70 to 2.34) NCT01706198 ↗

Publications

Drugs

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

Indications