Pulmonary Disease, Chronic Obstructive Clinical Trial
Official title:
Randomised, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Efficacy and Safety of 48 Weeks of Once Daily Treatment of Orally Inhaled BI 1744 CL (5 mcg [2 Actuations of 2.5 mcg] and 10 mcg [2 Actuations of 5 mcg]) Delivered by the Respimat® Inhaler, in Patients With Chronic Obstructive Pulmonary Disease (COPD)
This primary objective of this study is to compare two doses of BI 1744 CL inhalation
solution delivered by the Respimat® inhaler once daily to placebo in patients with chronic
obstructive pulmonary disease (COPD).
The safety of BI 1744 CL inhalation solution delivered through the Respimat inhaler will
also be compared to placebo.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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