Vilanterol
Sponsors
GlaxoSmithKline
Conditions
AsthmaPulmonary Disease, Chronic Obstructivechronic obstructive airways disease (COPD)
Phase 1
Phase 2
Phase 3
Study B2C112060: A Study of the Efficacy and Safety of Vilanterol Inhalation Powder in Adults and Adolescents With Persistent Asthma
CompletedNCT01181895
Start: 2010-09-01End: 2011-08-26Updated: 2017-11-08
Study to Evaluate the Effect of Fluticasone Furoate/Vilanterol on Survival in Subjects With Chronic Obstructive Pulmonary Disease
CompletedNCT01313676
Start: 2011-01-25End: 2015-07-15Updated: 2018-08-06
A 24-week Arterial Stiffness Study With Fluticasone Furoate/Vilanterol in COPD
CompletedNCT01336608
Start: 2011-03-04End: 2014-11-04Updated: 2017-11-08
RELOVAIR® Lung Deflation Study
CompletedNCT01691885
Start: 2012-11-30End: 2014-08-31Updated: 2016-10-27
Study Evaluating the Efficacy and Safety of Fluticasone Furoate/Vilanterol Inhalation Powder (FF/VI) Compared With Vilanterol Inhalation Powder (VI) in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
CompletedNCT02105974
Start: 2014-04-07End: 2015-07-08Updated: 2018-01-24
A Study to Compare the Efficacy of Fluticasone Furoate/Vilanterol Inhalation Powder With Usual Inhaled Corticosteroids (ICS)/Long Acting Beta Agonists (LABA) in Persistent Asthma
CompletedNCT02446418
Start: 2015-07-09End: 2017-07-20Updated: 2019-01-14
Phase 4
Study Evaluating the Effect of Fluticasone Furoate/ Vilanterol (FF/VI) Inhalation Powder Compared With Vilanterol (VI) Inhalation Powder on Bone Mineral Density (BMD) in Subjects With Chronic Obstructive Pulmonary Disease (COPD).
CompletedNCT01957150
Start: 2014-01-28End: 2018-03-26Updated: 2019-04-10
A 24-week treatment, multi-center, randomized, double-blind, double-dummy, parallel group study to compare Umeclidinium/Vilanterol, Umeclidinium, and Salmeterol in subjects with chronic obstructive pulmonary disease (COPD)
Active, not recruitingNL-OMON45687
Start: 2017-06-16Target: 80Updated: 2024-02-28