Systematic approach to selecting licensed drugs for repurposing in the treatment of progressive multiple sclerosis.


Journal

Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R

Informations de publication

Date de publication:
03 2021
Historique:
received: 16 06 2020
revised: 08 09 2020
accepted: 13 10 2020
pubmed: 14 11 2020
medline: 15 9 2021
entrez: 13 11 2020
Statut: ppublish

Résumé

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). 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. 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. We report a standardised approach for the identification of candidate drugs for repurposing in the treatment of progressive MS.

Identifiants

pubmed: 33184094
pii: jnnp-2020-324286
doi: 10.1136/jnnp-2020-324286
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

295-302

Subventions

Organisme : Medical Research Council
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: DB received compensation for consultancy activity from Canbex Therapeutics, Japan Tobacco, Lundbeck, InMune Bio, Merck, Novartis, and Roche in the past 3 years. AC received honoraria and travel support from Genzyme (a Sanofi company) prior to 2017. MC has received honoraria for educational events and/or consultancy from Biogen, Merck, Roche, AbbVie and Novartis. GG has received compensation for serving as a consultant in relation to multiple sclerosis drug development from AbbVie, Actelion, Atara Bio, Biogen, Celgene, EMD Serono, Japanese Tobacco, Sanofi-Genzyme, Genentech, GlaxoSmithKline, GW Pharma, Merck KGa, Novartis, Roche and Teva. LH holds a small number of GSK shares as part of her renumeration when she was an employee, which she left 4 years ago. DM received consultancy fees from Biogen, MedDay and SanofiGenzyme and Novartis. BN holds a patent regarding the treatment of demyelinating diseases including metformin: WO2019/206419 A1, Treatment for demyelinating disease. SP is cofounder, CSO and shareholder (>5%) of CITC Ltd and iSTEM Therapeutics, and cofounder and non-executive director at Asitia Therapeutics. LP-J is Head of Research at iSTEM Therapeutics. AW receives research support from Roche not associated with drug development or use.

Auteurs

Nick Cunniffe (N)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK ngc26@cam.ac.uk.

Khue Anh Vuong (KA)

Multiple Sclerosis Society, London, UK.

Debbie Ainslie (D)

Research Network, Multiple Sclerosis Society, London, UK.

David Baker (D)

Blizard Institute, Queen Mary University of London, London, UK.

Judy Beveridge (J)

Research Network, Multiple Sclerosis Society, London, UK.

Sorrel Bickley (S)

Multiple Sclerosis Society, London, UK.

Patrick Camilleri (P)

Independent consultant, Stevenage, UK.

Matthew Craner (M)

Department of Neurology, University of Oxford, Oxford, UK.

Denise Fitzgerald (D)

Wellcome-Wolfson Institute for Experimental Medicine, Queen's Univeristy, Belfast, UK.

Alerie G de la Fuente (AG)

Wellcome-Wolfson Institute for Experimental Medicine, Queen's Univeristy, Belfast, UK.

Gavin Giovannoni (G)

Blizard Institute, Queen Mary University of London, London, UK.

Emma Gray (E)

Multiple Sclerosis Society, London, UK.

Lorraine Hazlehurst (L)

Research Network, Multiple Sclerosis Society, London, UK.

Raj Kapoor (R)

Faculty of Brain Sciences, Queen Square Institute of Neurology, University College London, London, UK.

Ranjit Kaur (R)

Research Network, Multiple Sclerosis Society, London, UK.

David Kozlowski (D)

Research Network, Multiple Sclerosis Society, London, UK.

Brooke Lumicisi (B)

Multiple Sclerosis Society, London, UK.

Don Mahad (D)

Centre for Clinical Brain Sciences, Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh, UK.

Björn Neumann (B)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Alan Palmer (A)

University of Reading, Reading, Berkshire, UK.

Luca Peruzzotti-Jametti (L)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Stefano Pluchino (S)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Jennifer Robertson (J)

Multiple Sclerosis Society, London, UK.

Alan Rothaul (A)

Independent consultant, Woodstock, Oxfordshire, UK.

Lyndsey Shellard (L)

Research Network, Multiple Sclerosis Society, London, UK.

Kenneth J Smith (KJ)

Department of Neuroinflammation, Queen Square Institute of Neurology, University College London, London, UK.

Alastair Wilkins (A)

Department of Neurology, University of Bristol, Bristol, UK.

Anna Williams (A)

MS Centre, Centre for regenerative medicine, University of Edinburgh, Edinburgh, UK.

Alasdair Coles (A)

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

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Classifications MeSH