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Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease

INTRODUCTION: Combining long-acting muscarinic antagonists (LAMAs) and long-acting β(2)-agonists (LABAs) is beneficial in chronic obstructive pulmonary disease (COPD), as the two classes of bronchodilator have complementary modes of action. The optimal dose for the fixed-dose combination of the LAMA...

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Autores principales: Aalbers, René, Maleki-Yazdi, M. Reza, Hamilton, Alan, Waitere-Wijker, Stella, Zhao, Yihua, Amatto, Valeria C., Schmidt, Olaf, Bjermer, Leif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604503/
https://www.ncbi.nlm.nih.gov/pubmed/26404912
http://dx.doi.org/10.1007/s12325-015-0239-8
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author Aalbers, René
Maleki-Yazdi, M. Reza
Hamilton, Alan
Waitere-Wijker, Stella
Zhao, Yihua
Amatto, Valeria C.
Schmidt, Olaf
Bjermer, Leif
author_facet Aalbers, René
Maleki-Yazdi, M. Reza
Hamilton, Alan
Waitere-Wijker, Stella
Zhao, Yihua
Amatto, Valeria C.
Schmidt, Olaf
Bjermer, Leif
author_sort Aalbers, René
collection PubMed
description INTRODUCTION: Combining long-acting muscarinic antagonists (LAMAs) and long-acting β(2)-agonists (LABAs) is beneficial in chronic obstructive pulmonary disease (COPD), as the two classes of bronchodilator have complementary modes of action. The optimal dose for the fixed-dose combination of the LAMA tiotropium and the LABA olodaterol needed to be determined. In this phase II trial, the dose response of tiotropium on top of olodaterol was investigated in a free-dose combination, while other phase II studies have explored different doses of olodaterol on top of tiotropium, with both drugs delivered using the Respimat(®) inhaler. METHODS: This was a double-blind incomplete crossover trial in which 233 patients with moderate or severe COPD were randomized to receive four out of eight free-dose combinations of olodaterol (5 or 10 µg) and tiotropium (1.25, 2.5, or 5 µg) or placebo for 4 weeks each. Primary end point was trough forced expiratory volume in 1 s (FEV(1)) change from baseline (response) after 4 weeks. RESULTS: Addition of tiotropium 1.25, 2.5, and 5 µg to olodaterol 5 µg increased mean trough FEV(1) response by 0.054, 0.065, and 0.084 L, respectively; addition of tiotropium 1.25, 2.5, and 5 µg to olodaterol 10 µg increased mean trough FEV(1) response by 0.051, 0.083, and 0.080 L, respectively. All treatments were well tolerated and incidence of adverse events was similar with all treatments. CONCLUSIONS: Overall, a dose response for tiotropium on top of both doses of olodaterol was observed, with increasing improvements in trough FEV(1) compared to olodaterol alone as the tiotropium dose was increased. FUNDING: Boehringer Ingelheim. Trial registration: ClinicalTrials.gov number, NCT01040403. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-015-0239-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46045032015-10-19 Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease Aalbers, René Maleki-Yazdi, M. Reza Hamilton, Alan Waitere-Wijker, Stella Zhao, Yihua Amatto, Valeria C. Schmidt, Olaf Bjermer, Leif Adv Ther Original Research INTRODUCTION: Combining long-acting muscarinic antagonists (LAMAs) and long-acting β(2)-agonists (LABAs) is beneficial in chronic obstructive pulmonary disease (COPD), as the two classes of bronchodilator have complementary modes of action. The optimal dose for the fixed-dose combination of the LAMA tiotropium and the LABA olodaterol needed to be determined. In this phase II trial, the dose response of tiotropium on top of olodaterol was investigated in a free-dose combination, while other phase II studies have explored different doses of olodaterol on top of tiotropium, with both drugs delivered using the Respimat(®) inhaler. METHODS: This was a double-blind incomplete crossover trial in which 233 patients with moderate or severe COPD were randomized to receive four out of eight free-dose combinations of olodaterol (5 or 10 µg) and tiotropium (1.25, 2.5, or 5 µg) or placebo for 4 weeks each. Primary end point was trough forced expiratory volume in 1 s (FEV(1)) change from baseline (response) after 4 weeks. RESULTS: Addition of tiotropium 1.25, 2.5, and 5 µg to olodaterol 5 µg increased mean trough FEV(1) response by 0.054, 0.065, and 0.084 L, respectively; addition of tiotropium 1.25, 2.5, and 5 µg to olodaterol 10 µg increased mean trough FEV(1) response by 0.051, 0.083, and 0.080 L, respectively. All treatments were well tolerated and incidence of adverse events was similar with all treatments. CONCLUSIONS: Overall, a dose response for tiotropium on top of both doses of olodaterol was observed, with increasing improvements in trough FEV(1) compared to olodaterol alone as the tiotropium dose was increased. FUNDING: Boehringer Ingelheim. Trial registration: ClinicalTrials.gov number, NCT01040403. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-015-0239-8) contains supplementary material, which is available to authorized users. Springer Healthcare 2015-09-24 2015 /pmc/articles/PMC4604503/ /pubmed/26404912 http://dx.doi.org/10.1007/s12325-015-0239-8 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Aalbers, René
Maleki-Yazdi, M. Reza
Hamilton, Alan
Waitere-Wijker, Stella
Zhao, Yihua
Amatto, Valeria C.
Schmidt, Olaf
Bjermer, Leif
Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title_full Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title_fullStr Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title_full_unstemmed Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title_short Randomized, Double-Blind, Dose-Finding Study for Tiotropium when Added to Olodaterol, Administered via the Respimat(®) Inhaler in Patients with Chronic Obstructive Pulmonary Disease
title_sort randomized, double-blind, dose-finding study for tiotropium when added to olodaterol, administered via the respimat(®) inhaler in patients with chronic obstructive pulmonary disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604503/
https://www.ncbi.nlm.nih.gov/pubmed/26404912
http://dx.doi.org/10.1007/s12325-015-0239-8
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