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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2013
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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. |
format | Online Article Text |
id | pubmed-3787816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
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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