drugset / Trial / NCT01711463

Relovair PD PK in Chinese Healthy Subjects

NCT01711463

Phase 1 Completed 16 enrolled GlaxoSmithKline
RandomizedCrossoverDouble-blindTreatment

Summary

In this study, fluticasone furoate (FF) and vilanterol (VI) in different dose combinations (50/25mcg, 100/25mcg and 200/25mcg) will be administered from a single dry powder device to evaluate the PD, PK, safety and tolerability of the combination in healthy Chinese subjects. The information gathered will be used as a support of the clinical development program of the fixed dose combination of FF/VI inhalation powder in Chinese population.

Timeline

Start
2012-12-05
Primary completion
2013-06-04
Completion
2013-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone Furoate Other / unclassified 50 ug Inhaled
Subject Fluticasone Furoate Other / unclassified 100 ug Inhaled
Subject Fluticasone Furoate Other / unclassified 200 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug Inhaled

Indications