drugset / Trial / NCT01397162
Dose Finding Study on BI54903 (Inhaled Corticosteroid) Administered Twice Daily Via Respimat® Inhaler in Asthmatic Patients Inadequately Controlled on Short-acting-beta-agonist (SABA) Therapy
RandomizedParallel-groupDouble-blindTreatment
Summary
The aim of the study is to assess and compare efficacy and safety of BI 54903 at 3 doses twice daily (b.i.d.) and fluticasone propionate hydrofluoroalkane metered dose inhaler (HFA MDI) at a dose of 88 mcg b.i.d and placebo b.i.d. over an 8-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled on short-acting-beta-agonist (SABA) prn therapy only as demonstrated by a decrease in forced expiratory volume in one second (FEV1) range10 to 25% and an asthma control questionnaire (ACQ-6) equal or greater than 1.5 at time of randomization
Timeline
- Start
- 2011-07-21
- Primary completion
- 2011-12-23
- Completion
- 2011-12-23
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ciclesonide | Other / unclassified | 22.7 unknown | Inhaled |
| Subject | Ciclesonide | Other / unclassified | 45.5 unknown | Inhaled |
| Subject | Ciclesonide | Other / unclassified | 90.9 unknown | Inhaled |
| Comparator | Fluticasone propionate | Other / unclassified | 88 ug | Inhaled |