drugset / Trial / NCT01899638

Pharmacokinetics Of Umeclidinium and Vilanterol in Healthy Chinese, a Randomized, Open Label, 3 Crossover Study.

NCT01899638

Phase 1 Completed 20 enrolled GlaxoSmithKline
RandomizedCrossoverOpen-labelTreatment

Summary

This study is to assess the pharmacokinetics (PK), safety and tolerability of UMEC (62.5µg and 125µg) and VI (25µg) as monotherapies and combinations in healthy Chinese subjects.

Timeline

Start
2013-05-20
Primary completion
2013-07-25
Completion
2013-07-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Umeclidinium Other / unclassified 62.5 ug Inhaled
Subject Umeclidinium Other / unclassified 125 ug Inhaled
Subject Vilanterol Other / unclassified 25 ug Inhaled