Literature DB >> 24696868

Umeclidinium/vilanterol fixed-dose combination for COPD.

J Gras1.   

Abstract

Chronic obstructive pulmonary disease (COPD) mortality is projected to increase by more than 30% in the next 10 years without interventions to cut risks, particularly tobacco smoke exposure. Umeclidinium/vilanterol at 62.5/25 μg is the fixed-dose combination of a long-acting antimuscarinic agent and a long-acting β2-adrenoceptor agonist that administered as dry powder by inhalation was developed for the maintenance treatment of COPD. The combination demonstrated its efficacy in phase III studies where the amelioration of lung function translated into subjective symptomatic improvements. Its long-term safety and tolerability were demonstrated in a 52-week study. Last December, umeclidinium/vilanterol 62.5/25 μg combination was approved, as Anoro™ Ellipta™, by the U.S. Food and Drug Administration (FDA) for maintenance treatment of COPD, being the first FDA-approved once-daily treatment for COPD that contains two long-acting bronchodilators in a single inhaler. It has been filed for approval with the European Medicines Agency. Copyright 2014 Prous Science, S.A.U. or its licensors. All rights reserved.

Entities:  

Keywords:  COPD; GSK-573719/GW-642444; Muscarinic M3 antagonists; Umeclidinium/vilanterol; β2-Adrenoceptor agonists

Mesh:

Substances:

Year:  2014        PMID: 24696868     DOI: 10.1358/dot.2014.50.3.2122119

Source DB:  PubMed          Journal:  Drugs Today (Barc)        ISSN: 1699-3993            Impact factor:   2.245


  2 in total

Review 1.  Umeclidinium/vilanterol: a review of its use as maintenance therapy in adults with chronic obstructive pulmonary disease.

Authors:  Hannah A Blair; Emma D Deeks
Journal:  Drugs       Date:  2015-01       Impact factor: 9.546

2.  Second M3 muscarinic receptor binding site contributes to bronchoprotection by tiotropium.

Authors:  Loes E M Kistemaker; Carolina R S Elzinga; Christofer S Tautermann; Michael P Pieper; Daniel Seeliger; Suraya Alikhil; Martina Schmidt; Herman Meurs; Reinoud Gosens
Journal:  Br J Pharmacol       Date:  2019-07-02       Impact factor: 8.739

  2 in total

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