drugset / Trial / NCT01431287

Tiotropium +Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)

NCT01431287 ↗

Phase 3 Completed 2539 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The overall objective of this study is to assess the efficacy and safety of 52 weeks once daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT Inhaler) compared with the individual components (tiotropium, olodaterol) (delivered by the RESPIMAT Inhaler) in patients with COPD.

Timeline

Start
2011-09
Primary completion
2013-11
Completion
2013-11

Outcome

Met primary endpoint

paper Both FDCs significantly improved FEV1 AUC0-3 and trough FEV1 response versus the mono-components in both studies. PMID 25573406 ↗

registry analysis (superiority or other test); Olodaterol (5 μg) vs Tio+Olo FDC (5/5 μg); p <0.0001; Adjusted mean difference 0.132 (95% CI 0.108 to 0.157) NCT01431287 ↗

registry analysis (superiority or other test); Olodaterol (5 μg) vs Tio+Olo FDC (5/5 μg); p = 0.0022; Adjusted mean difference -1.693 (95% CI -2.778 to -0.608) NCT01431287 ↗

release “pivotal Phase III TONADO® trials that demonstrated STIOLTO RESPIMAT provides significant improvements in lung function” prnewswire.com ↗

Publications

Drugs

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