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
—

Outcome

Met primary endpoint

registry analysis (superiority or other test); Placebo vs Olo 5 mcg qd; p <0.0001; Mean Difference (Final Values) 0.172 (95% CI 0.135 to 0.209); Mixed Models Analysis NCT00782210 ↗

registry analysis (superiority or other test); Placebo vs Olo 5 mcg qd; p <0.0001; Mean Difference (Final Values) 0.091 (95% CI 0.054 to 0.128); Mixed Models Analysis NCT00782210 ↗

Drugs

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