drugset / Trial / NCT00132925

An Efficacy and Safety Evaluation of Nasacort AQ in Children Ages 2-5 Years With Perennial Allergic Rhinitis

NCT00132925

Phase 3 Completed 460 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The purposes of this study are: * To demonstrate the efficacy of once daily administration of Nasacort AQ 110 µg compared with placebo in children 2-5 years of age with perennial allergic rhinitis; and * To assess the safety of Nasacort AQ 110 µg in children 2-5 years of age.

Timeline

Start
2003-11
Primary completion
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Triamcinolone Acetonide Other / unclassified 110 ug Intranasal