drugset / Trial / NCT01248975
Safety and Efficacy Study Adding GSK2190915 to Mid-dose Inhaled Corticosteroid/Long Acting Beta Agonist Combination Treatment for Asthma
RandomizedCrossoverQuadruple-blindDiagnostic
Summary
The primary objective of this study is to evaluate the efficacy and safety of adding GSK2190915 300mg or placebo tablets administered once daily to fluticasone propionate/salmeterol 250/50mcg inhalation powder administered twice daily in uncontrolled asthmatic subjects \> or = 18 years of age over the course of 6 weeks treatment. The secondary objectives are to undertake an exploratory analysis of the efficacy and safety of adding montelukast 10mg administered once daily to fluticasone propionate/salmeterol 250/50mcg inhalation powder administered twice daily and to investigate the pharmacokinetics and pharmacodynamics of GSK2190915 in uncontrolled asthmatic subjects \> or = 18 years of age over the course of 6 weeks treatment.
Timeline
- Start
- 2010-12
- Primary completion
- 2011-10
- Completion
- 2011-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | FIBOFLAPON | Small molecule | 300 mg | — |
| Comparator | Montelukast | Other / unclassified | 10 mg | — |
| Background | Fluticasone propionate | Other / unclassified | 250 ug | Inhaled |
| Background | Salmeterol | Other / unclassified | 50 ug | Inhaled |