At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomised, Double-blind, Double-dummy, Parallel-group Multicentre Study to Assess Efficacy and Safety of Fluticasone Furoate/GW642444 Inhalation Powder and Fluticasone Propionate/Salmeterol Inhalation Powder in the Treatment of Persistent Asthma in Adults and Adolescents
In Brief
A Phase 3 clinical trial evaluating Fluticasone furoate/Vilanterol Inhalation Powder, Fluticasone propionate/salmeterol Inhalation Powder, and 2 other interventions for Asthma. Completed, enrolled 810 participants across 63 sites in 6 countries.
Detailed Summary
The purpose of the study is to compare the efficacy and safety of fluticasone furoate/vilanterol (GW642444) inhalation powder administered once daily with fluticasone propionate/salmeterol administered twice daily in adolescent and adult subjects 12 years of age and older with persistent bronchial asthma over a 24-week period.
Study Details
Timeline
Interventions
Fluticasone furoate/Vilanterol Inhalation Powder inhaled orally once daily for 24 weeks
Fluticasone propionate/salmeterol Inhalation Powder inhaled orally twice daily for 24 weeks
Inhalation powder inhaled orally once daily for 24 weeks
Inhalation powder inhaled orally twice daily for 24 weeks