Evaluation of Tiotropium 2.5 and 5 Mcg Once Daily Delivered Via the Respimat® Inhaler Compared to Placebo and Salmeterol HydroFluoroAlkane (HFA) Metered Dose Inhaler (MDI) (50 Mcg Twice Daily) in Patient With Moderate Persistent Asthma II



Status:Archived
Conditions:Asthma
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:August 2010

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A Phase III Randomised, Double-blind, Placebo-controlled, Parallel-group Trial to Evaluate Efficacy and Safety of Tiotropium Inhalation Solution Delivered Via Respimat® Inhaler (2.5 and 5 µg Once Daily) Compared With Placebo and Salmeterol HFA MDI (50 µg Twice Daily) Over 24 Weeks in Moderate Persistent Asthma


The aim of this trial is to evaluate the efficacy and safety of 2.5 and 5 mcg tiotropium
over a 24-week treatment period as compared to placebo and salmeterol (50 mcg twice daily).
Tiotropium inhalation solution delivered by the Respimat® inhaler will be examined on top of
maintenance treatment with inhaled corticosteroid controller medication in patients with
moderate persistent asthma. Efficacy and safety will be assessed by measuring effects on
lung function, effects on asthma exacerbations, effects on quality of life, effects on
asthma control, effects on health care resource utilisation, and number of adverse events.



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