Natalizumab (Tysabri) for secondary progressive multiple sclerosis
NIHR HSRIC
Record ID 32016000347
English
Authors' objectives:
Natalizumab (Tysabri) is intended for the treatment of secondary progressive multiple sclerosis (SPMS) in patients who have progressed from relapsing remitting MS. If licensed, natalizumab will offer an additional treatment option for patients with SPMS, a group who currently have few effective therapies available. No disease-modifying drugs are currently licensed specifically for SPMS. Natalizumab is a selective adhesion-molecule inhibitor that binds to the α4-subunit of human integrins, which are highly expressed on the surface of all leukocytes except neutrophils. The interaction between α4β1 and its targets is an important component of pathological inflammation in the brain and disruption of these interactions leads to reduced inflammation. Natalizumab is licensed in the EU for the treatment of highly active relapsing remitting multiple sclerosis (RRMS) in patients aged 18 years and over with high disease activity despite treatment with a beta-interferon or glatiramer acetate; or patients aged 18 years and over with rapidly evolving severe RRMS.
MS is a chronic immune-mediated condition of the central nervous system characterised by demyelination and axonal degeneration. MS is incurable and progressive in the majority of people, resulting in a low incidence but high prevalence. The prevalence of MS in England is approximately 0.16%, equivalent to approximately 85,600 affected people. About 75% of people whose disease pattern begins with relapsing and remitting symptoms later develop SPMS, 30-40% of those with RRMS develop SPMS within ten years of diagnosis. In 2013-14 there were 44,335 admissions for MS in England, resulting in 53,554 bed days and 46,584 finished consultant episodes. In England and Wales, 1,100 deaths due to MS were registered in 2013.
The aim of effective therapy is to relieve symptoms, prevent or delay disability arising from disease progression and promote tissue repair to treat established progression. Natalizumab is currently in one phase III clinical trial comparing its effect on progression of disability against treatment with placebo. This trial is expected to complete in March 2017.
Details
Project Status:
Completed
Year Published:
2015
URL for published report:
http://www.hsric.nihr.ac.uk/topics/natalizumab-tysabri-for-secondary-progressive-multiple-sclerosis/
English language abstract:
An English language summary is available
Publication Type:
Not Assigned
Country:
England, United Kingdom
MeSH Terms
- Humans
- Antibodies, Monoclonal, Humanized
- Multiple Sclerosis
- Multiple Sclerosis, Chronic Progressive
- Natalizumab
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 Research&Intelligence Centre (NIHR HSRIC)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.