drugset / Trial / NCT01964352

Tiotropium + Olodaterol Fixed Dose Combination (FDC) in Chronic Obstructive Pulmonary Disease (OTEMTO 1)

NCT01964352 ↗

Phase 3 Completed 813 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this study is to assess the efficacy and safety of 12 weeks once daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the Respimat inhaler) compared with tiotropium and placebo in patients with COPD.

Timeline

Start
2013-11
Primary completion
2014-10
Completion
2014-11

Outcome

Met primary endpoint

registry analysis (superiority or other test); Placebo vs Tiotropium 5 μg + Olodaterol 5 μg; p <0.0001; Mean Difference (Final Values) 0.331 (95% CI 0.293 to 0.369) NCT01964352 ↗

registry analysis (superiority or other test); Placebo vs Tiotropium 5 μg + Olodaterol 5 μg; p <0.0001; Mean Difference (Final Values) 0.162 (95% CI 0.0124 to 0.200) NCT01964352 ↗

registry analysis (superiority or other test); Placebo vs Tiotropium 5 μg + Olodaterol 5 μg; p <0.0001; Mean Difference (Final Values) -4.894 (95% CI -6.904 to -2.884) NCT01964352 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Olodaterol Small molecule 5 ug Inhaled
Comparator Tiotropium Other / unclassified 2.5 ug Inhaled
Comparator Tiotropium Other / unclassified 5 ug Inhaled