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dc.contributor.authorMao, Zen_US
dc.contributor.authorÁlvarez-Gonzalez, Cen_US
dc.contributor.authorDe Trane, Sen_US
dc.contributor.authorYildiz, Oen_US
dc.contributor.authorAlbor, Cen_US
dc.contributor.authorDoctor, Gen_US
dc.contributor.authorSoon, Den_US
dc.contributor.authorPepper, Gen_US
dc.contributor.authorTurner, BPen_US
dc.contributor.authorMarta, Men_US
dc.contributor.authorMathews, Jen_US
dc.contributor.authorGiovannoni, Gen_US
dc.contributor.authorBaker, Den_US
dc.contributor.authorSchmierer, Ken_US
dc.date.accessioned2018-08-24T11:36:12Z
dc.date.available2018-05-04en_US
dc.date.issued2018-04en_US
dc.date.submitted2018-08-16T06:18:22.383Z
dc.identifier.issn2055-2173en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/43785
dc.description.abstractBackground: A considerable number of people with multiple sclerosis (pwMS) live in low- and middle-income countries (LMIC), where lack of resource adversely affects access to effective disease-modifying treatment. Objective: The objective of this commentary is to propose a useful cost-effective disease-modifying treatment option for pwMS in LMIC with potential high efficacy and high convenience to the pwMS and treating physician.Viewpoint: We propose using generic 2-chloro-2'-deoxyadenosine (cladribine), a small molecule licensed for treatment of people with hairy cell leukaemia, as a solution of this significant equity imbalance. Cladribine has been shown in phase II and III trials to be a highly effective disease-modifying treatment for pwMS, and its adverse effect profile is comparable with any DMT currently licensed in high-income economies where an oral preparation has recently been licensed by the European Medicines Agency. Conclusion: Our viewpoint takes into account experience we have gathered over the past three years in the use of generic cladribine to treat pwMS. Whilst here we focus on MS, there is significant potential for use of cladribine in other conditions that could benefit from its mechanism of action.en_US
dc.description.sponsorshipZM has been supported by an ECTRIMS Clinical Training Fellowship (FS-E ECTRIMS2016-0042).en_US
dc.format.extent2055217318783767 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofMult Scler J Exp Transl Clinen_US
dc.subjectCladribineen_US
dc.subjectdisease-modifying treatmenten_US
dc.subjectlow- and middle-income countriesen_US
dc.subjectmultiple sclerosisen_US
dc.subjectoff-labelen_US
dc.titleCladribine: Off-label disease modification for people with multiple sclerosis in resource-poor settings?en_US
dc.typeArticle
dc.identifier.doi10.1177/2055217318783767en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/30090639en_US
pubs.issue2en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublished onlineen_US
pubs.volume4en_US
dcterms.dateAccepted2018-05-04en_US


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