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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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Detalles Bibliográficos
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
Descripción
Sumario: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.