drugset / Trial / NCT02164539
Evaluation of Umeclidinium Bromide in Combination With Fluticasone Furoate in COPD Subjects With an Asthmatic Component
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |