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Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial

BACKGROUND: The aim of this work was to investigate the safety and efficacy of single-inhaler triple therapy with 12.5 μg glycopyrronium (GB)/12 μg formoterol fumarate (FF)/250 μg fluticasone propionate (FP), compared to 50 μg GB co-administered with a fixed dose of 12 μg FF/250 μg FP in subjects wi...

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Autores principales: Salvi, Sundeep, Balki, Akash, Krishnamurthy, Srikanth, Panchal, Sagar, Patil, Saiprasad, Kodgule, Rahul, Khandagale, Hitesh, Pendse, Amol, Wu, Wen, Rangwala, Shabbir, Tandon, Monika, Barkate, Hanmant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311133/
https://www.ncbi.nlm.nih.gov/pubmed/34322547
http://dx.doi.org/10.1183/23120541.00255-2021
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author Salvi, Sundeep
Balki, Akash
Krishnamurthy, Srikanth
Panchal, Sagar
Patil, Saiprasad
Kodgule, Rahul
Khandagale, Hitesh
Pendse, Amol
Wu, Wen
Rangwala, Shabbir
Tandon, Monika
Barkate, Hanmant
author_facet Salvi, Sundeep
Balki, Akash
Krishnamurthy, Srikanth
Panchal, Sagar
Patil, Saiprasad
Kodgule, Rahul
Khandagale, Hitesh
Pendse, Amol
Wu, Wen
Rangwala, Shabbir
Tandon, Monika
Barkate, Hanmant
author_sort Salvi, Sundeep
collection PubMed
description BACKGROUND: The aim of this work was to investigate the safety and efficacy of single-inhaler triple therapy with 12.5 μg glycopyrronium (GB)/12 μg formoterol fumarate (FF)/250 μg fluticasone propionate (FP), compared to 50 μg GB co-administered with a fixed dose of 12 μg FF/250 μg FP in subjects with COPD. METHODS: This was a phase 3, randomised, double-blind, active-control, parallel-group, noninferiority study conducted at 20 sites across India. COPD patients aged ≥40 to ≤75 years, with forced expiratory volume in 1 s (FEV(1))/forced vital capacity (FVC) <0.70, using mono/dual therapy with inhaled corticosteroids (ICSs), long-acting muscarinic antagonists (LAMAs), or long-acting β-agonists (LABAs) for ≥1 month, were included. Subjects were randomised 1:1 to GB/FF/FP or GB+FF/FP for 12 weeks. The primary efficacy end-point was the change from baseline in trough FEV(1) at the end of 12 weeks. The study is registered with the Clinical Trials Registry of India (identifier number: CTRI/2019/01/017156). RESULTS: Between 23 March 2019 and 14 February 2020, 396 subjects were enrolled, with 198 patients each in the fixed-triple (GB/FF/FP) and open-triple (GB+FF/FP) groups. The difference in least-square mean (LSM) changes in pre-dose FEV(1) from baseline at 12 weeks was noninferior between the groups (p<0.05). The LSM change from baseline in post-dose FEV(1) was comparable (p=0.38). A superiority test showed comparable efficacy (p=0.12) for the difference in mean change from baseline in trough FEV(1) between the groups. Adverse events (mild or moderate) were recorded in 25.3% and 24.9% of subjects in the GB/FF/FP and GB+FF/FP groups. CONCLUSIONS: Fixed triple therapy with GB/FF/FP provides comparable bronchodilation and lung function improvement as open-triple therapy. It is safe and well tolerated in symptomatic COPD patients with a history of exacerbations.
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spelling pubmed-83111332021-07-27 Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial Salvi, Sundeep Balki, Akash Krishnamurthy, Srikanth Panchal, Sagar Patil, Saiprasad Kodgule, Rahul Khandagale, Hitesh Pendse, Amol Wu, Wen Rangwala, Shabbir Tandon, Monika Barkate, Hanmant ERJ Open Res Original Research Articles BACKGROUND: The aim of this work was to investigate the safety and efficacy of single-inhaler triple therapy with 12.5 μg glycopyrronium (GB)/12 μg formoterol fumarate (FF)/250 μg fluticasone propionate (FP), compared to 50 μg GB co-administered with a fixed dose of 12 μg FF/250 μg FP in subjects with COPD. METHODS: This was a phase 3, randomised, double-blind, active-control, parallel-group, noninferiority study conducted at 20 sites across India. COPD patients aged ≥40 to ≤75 years, with forced expiratory volume in 1 s (FEV(1))/forced vital capacity (FVC) <0.70, using mono/dual therapy with inhaled corticosteroids (ICSs), long-acting muscarinic antagonists (LAMAs), or long-acting β-agonists (LABAs) for ≥1 month, were included. Subjects were randomised 1:1 to GB/FF/FP or GB+FF/FP for 12 weeks. The primary efficacy end-point was the change from baseline in trough FEV(1) at the end of 12 weeks. The study is registered with the Clinical Trials Registry of India (identifier number: CTRI/2019/01/017156). RESULTS: Between 23 March 2019 and 14 February 2020, 396 subjects were enrolled, with 198 patients each in the fixed-triple (GB/FF/FP) and open-triple (GB+FF/FP) groups. The difference in least-square mean (LSM) changes in pre-dose FEV(1) from baseline at 12 weeks was noninferior between the groups (p<0.05). The LSM change from baseline in post-dose FEV(1) was comparable (p=0.38). A superiority test showed comparable efficacy (p=0.12) for the difference in mean change from baseline in trough FEV(1) between the groups. Adverse events (mild or moderate) were recorded in 25.3% and 24.9% of subjects in the GB/FF/FP and GB+FF/FP groups. CONCLUSIONS: Fixed triple therapy with GB/FF/FP provides comparable bronchodilation and lung function improvement as open-triple therapy. It is safe and well tolerated in symptomatic COPD patients with a history of exacerbations. European Respiratory Society 2021-07-26 /pmc/articles/PMC8311133/ /pubmed/34322547 http://dx.doi.org/10.1183/23120541.00255-2021 Text en Copyright ©The authors 2021 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Salvi, Sundeep
Balki, Akash
Krishnamurthy, Srikanth
Panchal, Sagar
Patil, Saiprasad
Kodgule, Rahul
Khandagale, Hitesh
Pendse, Amol
Wu, Wen
Rangwala, Shabbir
Tandon, Monika
Barkate, Hanmant
Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title_full Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title_fullStr Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title_full_unstemmed Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title_short Efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with COPD: a double-blind, randomised controlled trial
title_sort efficacy and safety of single-inhaler triple therapy of glycopyrronium, formoterol and fluticasone in patients with copd: a double-blind, randomised controlled trial
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311133/
https://www.ncbi.nlm.nih.gov/pubmed/34322547
http://dx.doi.org/10.1183/23120541.00255-2021
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