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A new class of bronchodilator improves lung function in COPD: a trial with GSK961081

GSK961081 is a bifunctional molecule demonstrating both muscarinic antagonist and β-agonist activities. This was a 4-week, multicentre, randomised, double-blind, double-dummy, placebo and salmeterol controlled parallel group study. Doses ranging across three twice-daily doses and three once-daily do...

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Autores principales: Wielders, Pascal L.M.L., Ludwig-Sengpiel, Andrea, Locantore, Nicholas, Baggen, Suus, Chan, Robert, Riley, John H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787816/
https://www.ncbi.nlm.nih.gov/pubmed/23429913
http://dx.doi.org/10.1183/09031936.00165712
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author Wielders, Pascal L.M.L.
Ludwig-Sengpiel, Andrea
Locantore, Nicholas
Baggen, Suus
Chan, Robert
Riley, John H.
author_facet Wielders, Pascal L.M.L.
Ludwig-Sengpiel, Andrea
Locantore, Nicholas
Baggen, Suus
Chan, Robert
Riley, John H.
author_sort Wielders, Pascal L.M.L.
collection PubMed
description GSK961081 is a bifunctional molecule demonstrating both muscarinic antagonist and β-agonist activities. This was a 4-week, multicentre, randomised, double-blind, double-dummy, placebo and salmeterol controlled parallel group study. Doses ranging across three twice-daily doses and three once-daily doses were assessed in moderate and severe chronic obstructive pulmonary disease (COPD) patients. Trough forced expiratory volume in 1 s (FEV(1)) at day 29 was the primary end-point. At days 1 and 28, 12-h FEV(1) spirometry was performed in all patients. A subset of patients underwent complete 24-h spirometry at day 28. The study recruited 436 patients. GSK961081 showed statistically and clinically significant differences from placebo in all doses and regimens for trough FEV(1) on day 29 (155–277 mL). The optimal total daily dose was 400 μg, either as 400 μg once daily or as 200 μg twice daily, with an improvement in day 29 trough FEV(1) of 215 mL and 249 mL, respectively. Other efficacy end-points also showed improvement. No effects were observed on glucose, potassium, heart rate, blood pressure and no dose–response effect was seen on corrected QT elongation. This study showed that GSK961081 is an effective bronchodilator in COPD and appeared to be safe and well tolerated.
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spelling pubmed-37878162013-11-01 A new class of bronchodilator improves lung function in COPD: a trial with GSK961081 Wielders, Pascal L.M.L. Ludwig-Sengpiel, Andrea Locantore, Nicholas Baggen, Suus Chan, Robert Riley, John H. Eur Respir J Original Article GSK961081 is a bifunctional molecule demonstrating both muscarinic antagonist and β-agonist activities. This was a 4-week, multicentre, randomised, double-blind, double-dummy, placebo and salmeterol controlled parallel group study. Doses ranging across three twice-daily doses and three once-daily doses were assessed in moderate and severe chronic obstructive pulmonary disease (COPD) patients. Trough forced expiratory volume in 1 s (FEV(1)) at day 29 was the primary end-point. At days 1 and 28, 12-h FEV(1) spirometry was performed in all patients. A subset of patients underwent complete 24-h spirometry at day 28. The study recruited 436 patients. GSK961081 showed statistically and clinically significant differences from placebo in all doses and regimens for trough FEV(1) on day 29 (155–277 mL). The optimal total daily dose was 400 μg, either as 400 μg once daily or as 200 μg twice daily, with an improvement in day 29 trough FEV(1) of 215 mL and 249 mL, respectively. Other efficacy end-points also showed improvement. No effects were observed on glucose, potassium, heart rate, blood pressure and no dose–response effect was seen on corrected QT elongation. This study showed that GSK961081 is an effective bronchodilator in COPD and appeared to be safe and well tolerated. European Respiratory Society 2013-10 2013-02-21 /pmc/articles/PMC3787816/ /pubmed/23429913 http://dx.doi.org/10.1183/09031936.00165712 Text en ©ERS 2013 http://creativecommons.org/licenses/by-nc/3.0/ ERJ Open articles are open access and distributed under the terms of the (Creative Commons Attribution Licence 3.0> (http://creativecommons.org/licenses/by-nc/3.0/) )
spellingShingle Original Article
Wielders, Pascal L.M.L.
Ludwig-Sengpiel, Andrea
Locantore, Nicholas
Baggen, Suus
Chan, Robert
Riley, John H.
A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title_full A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title_fullStr A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title_full_unstemmed A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title_short A new class of bronchodilator improves lung function in COPD: a trial with GSK961081
title_sort new class of bronchodilator improves lung function in copd: a trial with gsk961081
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787816/
https://www.ncbi.nlm.nih.gov/pubmed/23429913
http://dx.doi.org/10.1183/09031936.00165712
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