奥卡西平
医学
重新调整用途
药物重新定位
临床试验
纳塔利祖玛
拉莫三嗪
药理学
卡马西平
芬戈莫德
药品
多发性硬化
内科学
精神科
癫痫
生态学
生物
作者
Nick Cunniffe,Khue Anh Vuong,Debbie Ainslie,David Baker,Judy Beveridge,Sorrel Bickley,Patrick Camilleri,Matthew Craner,Denise Fitzgerald,Alerie Guzman de la Fuente,Gavin Giovannoni,Emma Gray,Lori Hazlehurst,Raj Kapoor,Ranjit Kaur,David J. Kozlowski,Brooke Lumicisi,Don J. Mahad,Björn Neumann,Alan M. Palmer
标识
DOI:10.1136/jnnp-2020-324286
摘要
Objective 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.
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