Clinical Development of Mepolizumab for the Treatment of Severe Eosinophilic Asthma: On the Path to Personalized Medicine.
Anti-IL-5
Biologic therapy
Mepolizumab
Severe eosinophilic asthma
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
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.e7Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.