Early and sustained symptom improvement with umeclidinium/vilanterol


Journal

Therapeutic advances in respiratory disease
ISSN: 1753-4666
Titre abrégé: Ther Adv Respir Dis
Pays: England
ID NLM: 101316317

Informations de publication

Date de publication:
Historique:
entrez: 29 5 2020
pubmed: 29 5 2020
medline: 2 6 2021
Statut: ppublish

Résumé

In chronic obstructive pulmonary disease (COPD), both the time needed for patients to gain symptom improvement with long-acting bronchodilator therapy and whether an early response is predictive of a sustained response is unknown. This study aimed to investigate how quickly meaningful symptom responses are seen in patients with COPD with bronchodilator therapy and whether these responses are sustained. Early MAXimisation of bronchodilation for improving COPD stability (EMAX) was a 24-week, double-blind, double-dummy, parallel-group trial that randomised patients to umeclidinium/vilanterol (UMEC/VI), umeclidinium or salmeterol. Daily Evaluating Respiratory Symptoms in COPD (E-RS:COPD) score and rescue salbutamol use were captured In the intent-to-treat population ( Patients with symptomatic COPD had greater potential for early symptom improvements with UMEC/VI NCT03034915, 2016-002513-22 (EudraCT Number).

Sections du résumé

BACKGROUND
In chronic obstructive pulmonary disease (COPD), both the time needed for patients to gain symptom improvement with long-acting bronchodilator therapy and whether an early response is predictive of a sustained response is unknown. This study aimed to investigate how quickly meaningful symptom responses are seen in patients with COPD with bronchodilator therapy and whether these responses are sustained.
METHODS
Early MAXimisation of bronchodilation for improving COPD stability (EMAX) was a 24-week, double-blind, double-dummy, parallel-group trial that randomised patients to umeclidinium/vilanterol (UMEC/VI), umeclidinium or salmeterol. Daily Evaluating Respiratory Symptoms in COPD (E-RS:COPD) score and rescue salbutamol use were captured
RESULTS
In the intent-to-treat population (
CONCLUSION
Patients with symptomatic COPD had greater potential for early symptom improvements with UMEC/VI
CLINICAL TRIAL REGISTRATION
NCT03034915, 2016-002513-22 (EudraCT Number).

Identifiants

pubmed: 32462979
doi: 10.1177/1753466620926949
pmc: PMC7278094
doi:

Substances chimiques

Adrenergic beta-2 Receptor Agonists 0
Benzyl Alcohols 0
Bronchodilator Agents 0
Chlorobenzenes 0
Drug Combinations 0
GSK573719 0
Muscarinic Antagonists 0
Quinuclidines 0
vilanterol 028LZY775B
Salmeterol Xinafoate 6EW8Q962A5

Banques de données

ClinicalTrials.gov
['NCT03034915']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1753466620926949

Références

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Auteurs

Edward M Kerwin (EM)

Crisor LLC, Clinical Research Institute, 3860 Crater Lake Ave., Medford, OR 97504, USA.

Isabelle H Boucot (IH)

GSK, Brentford, Middlesex, UK.

Claus F Vogelmeier (CF)

Department of Medicine, Pulmonary and Critical Care Medicine, University Medical Center Giessen and Marburg, Philipps-Universität Marburg, Member of the German Center for Lung Research (DZL), Germany.

Francois Maltais (F)

Centre de Pneumologie, Institut Universitaire de Cardiologie et de Pneumologie de Québec, Université Laval, Québec City, Québec, Canada.

Ian P Naya (IP)

GSK, Brentford, Middlesex, UK.
RAMAX Ltd, Bramhall, Cheshire, UK.

Lee Tombs (L)

Precise Approach Ltd, contingent worker on assignment at GSK, Stockley Park West, Uxbridge, Middlesex, UK.

Paul W Jones (PW)

GSK, Brentford, Middlesex, UK.

David A Lipson (DA)

Respiratory Clinical Sciences, GSK, Collegeville, PA, USA and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Tom Keeley (T)

GSK, Stockley Park West, Uxbridge, Middlesex, UK.

Leif Bjermer (L)

Respiratory Medicine and Allergology, Lund University, Lund, Sweden.

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Classifications MeSH