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Systematic approach to selecting licensed drugs for repurposing in the treatment of progressive multiple sclerosis.
Cunniffe, Nick; Vuong, Khue Anh; Ainslie, Debbie; Baker, David; Beveridge, Judy; Bickley, Sorrel; Camilleri, Patrick; Craner, Matthew; Fitzgerald, Denise; de la Fuente, Alerie G; Giovannoni, Gavin; Gray, Emma; Hazlehurst, Lorraine; Kapoor, Raj; Kaur, Ranjit; Kozlowski, David; Lumicisi, Brooke; Mahad, Don; Neumann, Björn; Palmer, Alan; Peruzzotti-Jametti, Luca; Pluchino, Stefano; Robertson, Jennifer; Rothaul, Alan; Shellard, Lyndsey; Smith, Kenneth J; Wilkins, Alastair; Williams, Anna; Coles, Alasdair.
Affiliation
  • Cunniffe N; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK ngc26@cam.ac.uk.
  • Vuong KA; Multiple Sclerosis Society, London, UK.
  • Ainslie D; Research Network, Multiple Sclerosis Society, London, UK.
  • Baker D; Blizard Institute, Queen Mary University of London, London, UK.
  • Beveridge J; Research Network, Multiple Sclerosis Society, London, UK.
  • Bickley S; Multiple Sclerosis Society, London, UK.
  • Camilleri P; Independent consultant, Stevenage, UK.
  • Craner M; Department of Neurology, University of Oxford, Oxford, UK.
  • Fitzgerald D; Wellcome-Wolfson Institute for Experimental Medicine, Queen's Univeristy, Belfast, UK.
  • de la Fuente AG; Wellcome-Wolfson Institute for Experimental Medicine, Queen's Univeristy, Belfast, UK.
  • Giovannoni G; Blizard Institute, Queen Mary University of London, London, UK.
  • Gray E; Multiple Sclerosis Society, London, UK.
  • Hazlehurst L; Research Network, Multiple Sclerosis Society, London, UK.
  • Kapoor R; Faculty of Brain Sciences, Queen Square Institute of Neurology, University College London, London, UK.
  • Kaur R; Research Network, Multiple Sclerosis Society, London, UK.
  • Kozlowski D; Research Network, Multiple Sclerosis Society, London, UK.
  • Lumicisi B; Multiple Sclerosis Society, London, UK.
  • Mahad D; Centre for Clinical Brain Sciences, Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh, UK.
  • Neumann B; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Palmer A; University of Reading, Reading, Berkshire, UK.
  • Peruzzotti-Jametti L; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Pluchino S; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Robertson J; Multiple Sclerosis Society, London, UK.
  • Rothaul A; Independent consultant, Woodstock, Oxfordshire, UK.
  • Shellard L; Research Network, Multiple Sclerosis Society, London, UK.
  • Smith KJ; Department of Neuroinflammation, Queen Square Institute of Neurology, University College London, London, UK.
  • Wilkins A; Department of Neurology, University of Bristol, Bristol, UK.
  • Williams A; MS Centre, Centre for regenerative medicine, University of Edinburgh, Edinburgh, UK.
  • Coles A; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
J Neurol Neurosurg Psychiatry ; 92(3): 295-302, 2021 03.
Article in En | MEDLINE | ID: mdl-33184094
ABSTRACT

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multiple Sclerosis, Chronic Progressive / Drug Repositioning Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2021 Document type: Article Affiliation country: United kingdom Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multiple Sclerosis, Chronic Progressive / Drug Repositioning Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2021 Document type: Article Affiliation country: United kingdom Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM