drugset / Trial / NCT00117325

Study Of Adults And Adolescents With Vasomotor Rhinitis

NCT00117325

Phase 3 Completed 352 enrolled GlaxoSmithKline
RandomizedParallel-groupTreatment

Summary

The primary objective of this study is to compare the efficacy and safety of GW685698X 100mcg once daily (QD) aqueous nasal spray with vehicle placebo nasal spray in adult and adolescent subjects (12 years of age and older) with vasomotor rhinitis (VMR).

Timeline

Start
2005-07-11
Primary completion
2006-02-09
Completion
2006-02-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone Furoate Other / unclassified 100 ug Intranasal

Indications