Reslizumab for eosinophilic asthma

NIHR HSRIC
Record ID 32016000339
English
Authors' objectives: Reslizumab is intended to be used for the treatment of eosinophilic asthma in adults who are inadequately controlled on inhaled corticosteroids. If licensed, it will offer an additional treatment option for patients with eosinophilic asthma. Reslizumab is a monoclonal antibody which acts as an interleukin-5 (IL-5) receptor antagonist. IL-5 stimulates the production, activation and maturation of eosinophils. Infiltrating tissue eosinophils are potent proinflammatory leukocytes containing granule-derived basic proteins, lipid mediators, cytokines and chemokines. These contribute to airway inflammation and lung tissue remodelling that includes airway thickening, fibrosis and angiogenesis. Resilzumab does not currently have Marketing Authorisation in the EU for any indication. Asthma is a chronic disorder of the airways caused primarily by inflammation and constriction of the smooth muscle in airway walls (bronchoconstriction). In the UK around 5.4 million people are receiving treatment for asthma; the equivalent of 1 in 12 adults and 1 in 11 children. Of these, it is estimated that 3.0 million are female and 2.4 million are male. The Health Survey for England (2010) estimated the lifetime prevalence of diagnosed asthma to be 17% in women and 16% in men. Approximately 5% of asthma sufferers are described as therapy resistant and are unable to get good control of their asthma despite using high levels of anti-asthma medicines. In 2013-14, there were 60,636 hospital admissions for asthma in England, resulting in 138,140 bed days and 80,990 finished consultant episodes; 75% of these are avoidable. The management of asthma aims to control the disease while minimising adverse reactions to treatment: good control is characterised by no daytime symptoms, no night-time awakening due to asthma, normal lung function, no need for rescue medication, no exacerbations, and no limitations on activity including exercise. Reslizumab is currently in multiple phase III clinical trials comparing its effect on forced expiratory volume in 1 second (FEV1) and clinical asthma exacerbations against treatment with placebo. These trials are expected to complete by 2015.
Details
Project Status: Completed
Year Published: 2015
English language abstract: An English language summary is available
Publication Type: Not Assigned
Country: England, United Kingdom
MeSH Terms
  • Antibodies, Monoclonal, Humanized
  • Asthma
  • Pulmonary Eosinophilia
  • Anti-Asthmatic Agents
Contact
Organisation Name: NIHR Horizon Scanning Centre
Contact Address: The NIHR Horizon Scanning Centre, Department of Public Health, Epidemiology, and Biostatistics, School of Health and Population Sciences, University of Birmingham, 90 Vincent Drive, Edgbaston, Birmingham, B15 2SP. United Kingdom. Tel: +44 121 414 7831, Fax: +44 121 2269
Contact Name: c.packer@bham.ac.uk
Contact Email: c.packer@bham.ac.uk
Copyright: NIHR Horizon Scanning Centre (NIHR HSC)
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