drugset / Trial / NCT01502371

A Study of Mometasone Furoate Metered Dose Inhaler in Children With Persistent Asthma (P04223)

NCT01502371

Phase 2 Completed 583 enrolled Organon and Co
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to demonstrate the dose-related efficacy, by evaluating morning (AM) lung function at the end of the dosing interval (AM pre-dose percent predicted forced expiratory volume in one second \[FEV1\]) across 12 weeks of treatment, of three doses (50 mcg, 100 mcg, and 200 mcg) of Mometasone Furoate (MF) Metered Dose Inhaler (MDI) twice a day (BID) compared with Placebo in children 5 to 11 years of age, inclusive, with persistent asthma. The primary hypothesis of this study is that at least one dose of MF MDI BID increases lung function, defined as a significant increase in percent predicted FEV1, when compared to Placebo.

Timeline

Start
2012-01-25
Primary completion
2015-01-29
Completion
2015-01-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Mometasone furoate Other / unclassified 50 ug Inhaled
Subject Mometasone furoate Other / unclassified 100 ug Inhaled
Subject Mometasone furoate Other / unclassified 200 ug Inhaled

Indications