drugset / Trial / NCT01453023

Inhaled Fluticasone Furoate/Vilanterol Safety and Tolerability, PK and PD Study

NCT01453023

Phase 2 Completed 26 enrolled GlaxoSmithKline
RandomizedCrossoverTriple-blindTreatment

Summary

This study will investigate the safety and tolerability, pharmacokinetics, and pharmacodynamics of fluticasone furoate/vilanterol (FF/VI) 100/25mcg administered using the novel dry powder inhaler in children aged 5 to 11 years with persistent asthma.

Timeline

Start
2011-10
Primary completion
2012-06
Completion
2012-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fluticasone Furoate Other / unclassified 100 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug Inhaled

Indications