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Review
. 2021 Jun;81(9):1031-1063.
doi: 10.1007/s40265-021-01526-w. Epub 2021 Jun 4.

Failed, Interrupted, or Inconclusive Trials on Neuroprotective and Neuroregenerative Treatment Strategies in Multiple Sclerosis: Update 2015-2020

Affiliations
Review

Failed, Interrupted, or Inconclusive Trials on Neuroprotective and Neuroregenerative Treatment Strategies in Multiple Sclerosis: Update 2015-2020

Niklas Huntemann et al. Drugs. 2021 Jun.

Abstract

In the recent past, a plethora of drugs have been approved for the treatment of multiple sclerosis (MS). These therapeutics are mainly confined to immunomodulatory or immunosuppressive strategies but do not sufficiently address remyelination and neuroprotection. However, several neuroregenerative agents have shown potential in pre-clinical research and entered Phase I to III clinical trials. Although none of these compounds have yet proceeded to approval, understanding the causes of failure can broaden our knowledge about neuroprotection and neuroregeneration in MS. Moreover, most of the investigated approaches are characterised by consistent mechanisms of action and proved convincing efficacy in animal studies. Therefore, learning from their failure will help us to enforce the translation of findings acquired in pre-clinical studies into clinical application. Here, we summarise trials on MS treatment published since 2015 that have either failed or were interrupted due to a lack of efficacy, adverse events, or for other reasons. We further outline the rationale underlying these drugs and analyse the background of failure to gather new insights into MS pathophysiology and optimise future study designs. For conciseness, this review focuses on agents promoting remyelination and medications with primarily neuroprotective properties or unconventional approaches. Failed clinical trials that pursue immunomodulation are presented in a separate article.

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Conflict of interest statement

Niklas Huntemann: declares no conflicts of interest. Leoni Rolfes: declares no conflicts of interest. Marc Pawlitzki: declares no conflicts of interest. Tobias Ruck: received personal fees from Alexion, Biogen, Merck Serono, Sanofi-Genzyme, Roche, and Teva, grants from Alexion and Sanofi-Genzyme, and nonfinancial support from Merck Serono. Steffen Pfeuffer: received travel reimbursements from Sanofi Genzyme and Merck Serono, honoraria for lecturing from Sanofi Genzyme, Biogen, and Mylan Healthcare, and research support from Merck Serono, Diamed, and the German Multiple Sclerosis Society North Rhine-Westphalia. Heinz Wiendl: received grants from German Ministry for Education and Research (BMBF), Deutsche Forschungsgesellschaft (DFG), Else Kröner Fresenius Foundation, Fresenius Foundation, the European Union, Hertie Foundation, NRW Ministry of Education and Research, Interdisciplinary Center for Clinical Studies (IZKF) Muenster, Biogen, GlaxoSmithKline GmbH, Roche, and Sanofi-Genzyme; consulting fees from AbbVie, Actelion, Argenx, Biogen, EMD Serono, Idorsia, IGES, Immunic, Merck, Novartis, Roche, Sanofi-Aventis, the Swiss Multiple Sclerosis Society, and UCB; support for travel to meetings for other purposes from Alexion, Biogen, Cognomed, F. Hoffmann-La Roche Ltd., Hertie Foundation, Merck Serono, Novartis, Roche, Genzyme, Teva, and WebMD Global; fees for participation in review activities such as data monitoring boards from Polpharma Biologics; payment for lectures from Alexion, Biogen, Cognomed, F. Hoffmann-La Roche Ltd., Hertie Foundation, Merck Serono, Novartis, Roche, Genzyme, Teva, and WebMD Global; honorarium for expert testimony from the Drug Commission of the German Medical Association. Sven G. Meuth: received honoraria for lecturing and travel reimbursement for attending meetings from Almirall, Amicus Therapeutics Germany, Bayer Health Care, Biogen, Celgene, Diamed, Genzyme, MedDay Pharmaceuticals, Merck Serono, Novartis, Novo Nordisk, ONO Pharma, Roche, Sanofi-Aventis, Chugai Pharma, QuintilesIMS, and Teva. His research is funded by the German Ministry for Education and Research (BMBF), Bundesinstitut für Risikobewertung (BfR), Deutsche Forschungsgemeinschaft (DFG), Else Kröner Fresenius Foundation, Gemeinsamer Bundesausschuss (G-BA), German Academic Exchange Service, Hertie Foundation, Interdisciplinary Center for Clinical Studies (IZKF) Muenster, German Foundation Neurology and Alexion, Almirall, Amicus Therapeutics Germany, Biogen, Diamed, Fresenius Medical Care, Genzyme, HERZ Burgdorf, Merck Serono, Novartis, ONO Pharma, Roche, and Teva.

Figures

Fig. 1
Fig. 1
PRISMA flow diagram of the reviewed literature. AAN American Academy of Neurology, EU CT register European Union Clinical Trials register, ECTRIMS European Committee for Treatment and Research in Multiple Sclerosis

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