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Oral disease-modifying therapies for multiple sclerosis in the Middle Eastern and North African (MENA) region: an overview

Authors :
Dirk Deleu
Boulenouar Mesraoua
Beatriz CanibaƱo
Gayane Melikyan
Hassan Al Hail
Lubna El-Sheikh
Musab Ali
Hassan Al Hussein
Faiza Ibrahim
Yolande Hanssens
Source :
Current Medical Research and Opinion. 35:249-260
Publication Year :
2018
Publisher :
Informa UK Limited, 2018.

Abstract

The introduction of new disease-modifying therapies (DMTs) for remitting-relapsing multiple sclerosis (RRMS) has considerably transformed the landscape of therapeutic opportunities for this chronic disabling disease. Unlike injectable drugs, oral DMTs promote patient satisfaction and increase therapeutic adherence.This article reviews the salient features about the mode of action, efficacy, safety, and tolerability profile of approved oral DMTs in RRMS, and reviews their place in clinical algorithms in the Middle East and North Africa (MENA) region. A systematic review was conducted using a comprehensive search of MEDLINE, PubMed, Cochrane Database of Systematic Reviews (period January 1, 1995-January 31, 2018). Additional searches of the American Academy of Neurology and European Committee for Treatment and Research in Multiple Sclerosis abstracts from 2012-2017 were performed, in addition to searches of the Food and Drug Administration and European Medicines Agency websites, to obtain relevant safety information on these DMTs.Four oral DMTs: fingolimod, teriflunomide, dimethyl fumarate, and cladribine have been approved by the regulatory agencies. Based on the number needed to treat (NNT), the potential role of these DMTs in the management of active and highly active or rapidly evolving RRMS is assessed. Finally, the place of the oral DMTs in clinical algorithms in the MENA region is reviewed.

Details

ISSN :
14734877 and 03007995
Volume :
35
Database :
OpenAIRE
Journal :
Current Medical Research and Opinion
Accession number :
edsair.doi.dedup.....b447a03e117917da6fd432da2645fe79
Full Text :
https://doi.org/10.1080/03007995.2018.1476334