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dc.contributor.authorCunniffe, Nen_US
dc.contributor.authorVuong, KAen_US
dc.contributor.authorAinslie, Den_US
dc.contributor.authorBaker, Den_US
dc.contributor.authorBeveridge, Jen_US
dc.contributor.authorBickley, Sen_US
dc.contributor.authorCamilleri, Pen_US
dc.contributor.authorCraner, Men_US
dc.contributor.authorFitzgerald, Den_US
dc.contributor.authorde la Fuente, AGen_US
dc.contributor.authorGiovannoni, Gen_US
dc.contributor.authorGray, Een_US
dc.contributor.authorHazlehurst, Len_US
dc.contributor.authorKapoor, Ren_US
dc.contributor.authorKaur, Ren_US
dc.contributor.authorKozlowski, Den_US
dc.contributor.authorLumicisi, Ben_US
dc.contributor.authorMahad, Den_US
dc.contributor.authorNeumann, Ben_US
dc.contributor.authorPalmer, Aen_US
dc.contributor.authorPeruzzotti-Jametti, Len_US
dc.contributor.authorPluchino, Sen_US
dc.contributor.authorRobertson, Jen_US
dc.contributor.authorRothaul, Aen_US
dc.contributor.authorShellard, Len_US
dc.contributor.authorSmith, KJen_US
dc.contributor.authorWilkins, Aen_US
dc.contributor.authorWilliams, Aen_US
dc.contributor.authorColes, Aen_US
dc.date.accessioned2020-11-18T11:02:42Z
dc.date.available2020-10-13en_US
dc.date.issued2020-11-12en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68421
dc.description.abstractOBJECTIVE: To establish a rigorous, expert-led, evidence-based approach to the evaluation of licensed drugs for repurposing and testing in clinical trials of people with progressive multiple sclerosis (MS). METHODS: We long-listed licensed drugs with evidence of human safety, blood-brain barrier penetrance and demonstrable efficacy in at least one animal model, or mechanistic target, agreed by a panel of experts and people with MS to be relevant to the pathogenesis of progression. We systematically reviewed the preclinical and clinical literature for each compound, condensed this into a database of summary documents and short-listed drugs by scoring each one of them. Drugs were evaluated for immediate use in a clinical trial, and our selection was scrutinised by a final independent expert review. RESULTS: From a short list of 55 treatments, we recommended four treatments for immediate testing in progressive MS: R-α-lipoic acid, metformin, the combination treatment of R-α-lipoic acid and metformin, and niacin. We also prioritised clemastine, lamotrigine, oxcarbazepine, nimodipine and flunarizine. CONCLUSIONS: We report a standardised approach for the identification of candidate drugs for repurposing in the treatment of progressive MS.en_US
dc.languageengen_US
dc.relation.ispartofJ Neurol Neurosurg Psychiatryen_US
dc.titleSystematic approach to selecting licensed drugs for repurposing in the treatment of progressive multiple sclerosis.en_US
dc.typeArticle
dc.rights.holder© Author(s) (or their employer(s)) 2020.Published by BMJ.
dc.identifier.doi10.1136/jnnp-2020-324286en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33184094en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2020-10-13en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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