drugset / Trial / NCT01248975

Safety and Efficacy Study Adding GSK2190915 to Mid-dose Inhaled Corticosteroid/Long Acting Beta Agonist Combination Treatment for Asthma

NCT01248975

Phase 2 Completed 145 enrolled GlaxoSmithKline
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

EvaluationDrugModalityDoseRoute
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

Indications