drugset / Trial / NCT01502371
A Study of Mometasone Furoate Metered Dose Inhaler in Children With Persistent Asthma (P04223)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Mometasone furoate | Other / unclassified | 50 ug | Inhaled |
| Subject | Mometasone furoate | Other / unclassified | 100 ug | Inhaled |
| Subject | Mometasone furoate | Other / unclassified | 200 ug | Inhaled |