drugset / Trial / NCT00467740
Efficacy and Safety of 4 Weeks of Treatment With Inhaled BI 1744 CL in Patients With Asthma
Parallel-groupTreatment
Summary
The primary objective of this study is to determine the optimum dose(s) of BI 1744 CL inhalation solution delivered by the Respimat® inhaler for four weeks in patients with asthma. The selection of the optimum dose(s) will be based on bronchodilator efficacy (how well it helps your breathing), safety evaluations and pharmacokinetic evaluations (the amount of the medication found in your blood).
Timeline
- Start
- 2007-05
- Primary completion
- 2008-10
- Completion
- —
Outcome
Met primary endpoint
registry Placebo vs Olo 20 mcg qd; p = 0.0011; Mean Difference (Final Values) 0.147 (95% CI 0.059 to 0.234) NCT00467740 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Olodaterol | Small molecule | 2 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 5 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 10 ug | Inhaled |
| Subject | Olodaterol | Small molecule | 20 ug | Inhaled |