drugset / Trial / NCT00782210

12 / 48 Week Pivotal PFT vs PBO in COPD I

NCT00782210

Phase 3 Completed 625 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

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.

Timeline

Start
2008-11
Primary completion
2010-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Olodaterol Small molecule 5 ug Inhaled
Subject Olodaterol Small molecule 10 ug Inhaled