drugset / Trial / NCT01431274

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

NCT01431274 ↗

Phase 3 Completed 2624 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 Chronic Obstructive Pulmonary Disease (COPD).

Timeline

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

Outcome

Met primary endpoint

registry Olodaterol (5 μg) vs Tio+Olo FDC (5/5 μg); p <0.0001; Adjusted mean difference 0.123 (95% CI 0.100 to 0.146) NCT01431274 ↗

registry Tiotropium (5 μg) vs Tio+Olo FDC (5/5 μg); p <0.0001; Adjusted mean difference 0.117 (95% CI 0.094 to 0.140) NCT01431274 ↗

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

paper Statistically significant improvements in SGRQ total score versus the mono-components were only seen for tiotropium+olodaterol FDC 5/5 μg. PMID 25573406 ↗

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 —
Subject Tiotropium Other / unclassified 5 ug —