drugset / Trial / NCT01694771

Co-administration of Olodaterol Respimat® and Tiotropium Handihaler®

NCT01694771

Phase 3 Completed 1134 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The overall objective of this study is to assess efficacy and safety of 12 weeks, once daily, orally inhaled co-administration of olodaterol 5 µg (delivered by the Respimat® Inhaler) and tiotropium (delivered by the Handihaler® as Spiriva Handihaler®), compared to tiotropium (Spiriva Handihaler®) monotherapy on lung function in patients with COPD.

Timeline

Start
2012-09
Primary completion
2013-08
Completion
2013-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Olodaterol Small molecule 5 ug Inhaled
Background Tiotropium Other / unclassified 18 ug Inhaled