Trials / Completed
CompletedNCT00383240
Effects of Mometasone Furoate/Formoterol Combination Versus Mometasone Furoate Alone in Persistent Asthmatics (Study P04334AM1)(COMPLETED)
A 26-Week Placebo-Controlled Efficacy and Safety Study of Mometasone Furoate/Formoterol Fumarate Combination Formulation Compared With Mometasone Furoate and Formoterol Monotherapy in Subjects With Persistent Asthma Previously Treated With Medium-Dose Inhaled Glucocorticosteroids
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 781 (actual)
- Sponsor
- Organon and Co · Industry
- Sex
- All
- Age
- 12 Years
- Healthy volunteers
- Not accepted
Summary
This is a randomized, multi-center, double-blind, double-dummy, placebo-controlled, parallel-group study, evaluating the efficacy of mometasone furoate (MF) /formoterol fumarate (F)\[MF/F\] metered dose inhaler (MDI) versus MF for 26 weeks. Prior to the 26-week double-blind Treatment Period, subjects will receive open-label MF MDI 200 mcg twice daily (BID) for 2 to 3 weeks during the Run-in Period. Efficacy will be measured by The Area Under the Curve From 0 to 12 Hours \[AUC\](0-12 hours) of the Change From Baseline to the Week 12 Endpoint in Forced Expiratory Volume in One Second (FEV1) \[Time Frame: Baseline to Week 12\] and Time-to-First Severe Asthma Exacerbation across the 26-week treatment period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | mometasone furoate/formoterol fumarate combination MDI 200/10 mcg BID | MF/F 200/10 mcg via a metered dose inhaler (MDI) twice daily for 26 weeks |
| DRUG | Mometasone furoate MDI (MF MDI) 200 mcg | MF 200 mcg via metered dose inhaler twice daily for 26 weeks |
| DRUG | formoterol fumarate 10 mcg | F via metered dose inhaler 10 mcg twice a day for 26 weeks |
| DRUG | Placebo | Placebo metered dose inhaler twice a day for 26 weeks |
Timeline
- Start date
- 2006-09-01
- Primary completion
- 2008-09-01
- Completion
- 2008-09-01
- First posted
- 2006-10-03
- Last updated
- 2024-05-20
- Results posted
- 2011-03-07
Source: ClinicalTrials.gov record NCT00383240. Inclusion in this directory is not an endorsement.