A Study to Compare the Efficacy and Safety of Different Dosings of Olodaterol Administered With the Respimat® Inhaler in Patients With Moderate to Severe Asthma
Completed
Boehringer Ingelheim
Phase 2
2011-03-01
This study will compare efficacy and safety of different regimens of olodaterol
administration in asthma (once daily, twice daily) with placebo in a complete cross-over
design each within one of the two daily dose groups (medium or high daily dose).
The aim of the study is to establish the olodaterol dose in the ethanolic fixed dose
combination (FDC) with BI 54903 which is equivalent in bronchodilator effect and systemic
exposure to the 5 µg olodaterol reference dose in the aqueous inhalation solution (AIS).
Tiotropium+Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Completed
Boehringer Ingelheim
Phase 3
2011-09-01
The overall objective of this study is to assess the efficacy and safety of 52 weeks once
daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT
Inhaler) compared with the individual components ( tiotropium, olodaterol) (delivered by the
RESPIMAT Inhaler) in patients with Chronic Obstructive Pulmonary Disease (COPD).
Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)
Completed
Boehringer Ingelheim
Phase 3
2011-09-01
The overall objective of this study is to assess the efficacy and safety of 52 weeks once
daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT
Inhaler) compared with the individual components (tiotropium, olodaterol) (delivered by the
RESPIMAT Inhaler) in patients with COPD.
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