drugset / Trial / NCT00467740

Efficacy and Safety of 4 Weeks of Treatment With Inhaled BI 1744 CL in Patients With Asthma

NCT00467740 ↗

Phase 2 Completed 296 enrolled Boehringer Ingelheim
Parallel-groupTreatment

Summary

The primary objective of this study is to determine the optimum dose(s) of BI 1744 CL inhalation solution delivered by the Respimat® inhaler for four weeks in patients with asthma. The selection of the optimum dose(s) will be based on bronchodilator efficacy (how well it helps your breathing), safety evaluations and pharmacokinetic evaluations (the amount of the medication found in your blood).

Timeline

Start
2007-05
Primary completion
2008-10
Completion
—

Outcome

Met primary endpoint

registry Placebo vs Olo 20 mcg qd; p = 0.0011; Mean Difference (Final Values) 0.147 (95% CI 0.059 to 0.234) NCT00467740 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Olodaterol Small molecule 2 ug Inhaled
Subject Olodaterol Small molecule 5 ug Inhaled
Subject Olodaterol Small molecule 10 ug Inhaled
Subject Olodaterol Small molecule 20 ug Inhaled

Indications