Clinical Development of Mepolizumab for the Treatment of Severe Eosinophilic Asthma: On the Path to Personalized Medicine.


Journal

The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220

Informations de publication

Date de publication:
03 2021
Historique:
received: 15 04 2020
revised: 15 07 2020
accepted: 12 08 2020
pubmed: 6 9 2020
medline: 25 5 2021
entrez: 5 9 2020
Statut: ppublish

Résumé

The development of mepolizumab, an anti-IL-5 monoclonal antibody for the treatment of severe eosinophilic asthma, is an example of a clinical development program that evolved over time based on sound, basic scientific principles. Initial clinical data on the effects of mepolizumab on lung function in a general asthmatic population were disappointing. However, it became clear that mepolizumab may be more effective against other clinical endpoints, particularly asthma exacerbations, in patients with more severe disease. Furthermore, a developing understanding of asthma disease pathobiology led to the identification of an appropriate target population and predictive biomarker for mepolizumab treatment: patients with severe eosinophilic asthma and blood eosinophil count. Mepolizumab use provides clinically meaningful benefits in this target population, fulfilling an unmet need. This Clinical Commentary Review describes the clinical development of mepolizumab and details of how this program informed the development of other biologic therapies in patients with severe asthma. This account highlights how a personalized approach toward treatment of patients with severe eosinophilic asthma, supported by a large body of scientific evidence, ultimately led to new and effective treatments and improved patient outcomes.

Identifiants

pubmed: 32889223
pii: S2213-2198(20)30871-0
doi: 10.1016/j.jaip.2020.08.039
pii:
doi:

Substances chimiques

Anti-Asthmatic Agents 0
Antibodies, Monoclonal, Humanized 0
mepolizumab 90Z2UF0E52

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1121-1132.e7

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Ian D Pavord (ID)

Nuffield Department of Medicine and Oxford Respiratory NIHR BRC, University of Oxford, Oxford, United Kingdom.

Andrew Menzies-Gow (A)

Respiratory Medicine, Royal Brompton Hospital, London, United Kingdom.

Roland Buhl (R)

Pulmonary Department, Mainz University Hospital, Mainz, Germany.

Pascal Chanez (P)

Aix-Marseille Université, INSERM CV2N, APHM CIC NORD, Marseille, France.

Mark Dransfield (M)

Division of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, Ala.

Njira Lugogo (N)

Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, Mich.

Oliver N Keene (ON)

Biostatistics, GSK, Stockley Park, Uxbridge, Middlesex, United Kingdom.

Eric S Bradford (ES)

Respiratory Therapeutic Area, GSK, Research Triangle Park, NC.

Steve W Yancey (SW)

Respiratory Therapeutic Area, GSK, Research Triangle Park, NC. Electronic address: steve.w.yancey@gsk.com.

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Classifications MeSH