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Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments
Multiple sclerosis treatment made substantial headway during the last two decades with the implementation of therapeutics with new modes of action and routes of application. We are now in the situation that second-generation molecules, approved since 2018, are on the market, characterized by reduced...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307218/ https://www.ncbi.nlm.nih.gov/pubmed/35869335 http://dx.doi.org/10.1007/s40263-022-00939-9 |
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author | Faissner, Simon Gold, Ralf |
author_facet | Faissner, Simon Gold, Ralf |
author_sort | Faissner, Simon |
collection | PubMed |
description | Multiple sclerosis treatment made substantial headway during the last two decades with the implementation of therapeutics with new modes of action and routes of application. We are now in the situation that second-generation molecules, approved since 2018, are on the market, characterized by reduced side effects using a more tailored therapeutic approach. Diroximel fumarate is a second-generation fumarate with reduced gastrointestinal side effects. Moreover, several novel, selective, sphingosine-1-phosphate receptor modulators with reduced off-target effects have been developed; namely siponimod, ozanimod, and ponesimod; all oral formulations. B-cell-targeted therapies such as ocrelizumab, given intravenously, and since 2021 ofatumumab, applied subcutaneously, complement the spectrum of novel therapies. The glycoengineered antibody ublituximab is the next anti-CD20 therapy about to be approved. Within the next years, oral inhibitors of Bruton’s tyrosine kinase, currently under investigation in several phase III trials, may be licensed for multiple sclerosis. Those developments currently offer an individualized multiple sclerosis therapy, targeting patient needs with substantial effects on relapses, disability progression, and implications for daily life. In this up-to-date review, we provide a holistic overview about novel developments of the therapeutic landscape and upcoming approaches for multiple sclerosis treatment. |
format | Online Article Text |
id | pubmed-9307218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-93072182022-07-25 Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments Faissner, Simon Gold, Ralf CNS Drugs Review Article Multiple sclerosis treatment made substantial headway during the last two decades with the implementation of therapeutics with new modes of action and routes of application. We are now in the situation that second-generation molecules, approved since 2018, are on the market, characterized by reduced side effects using a more tailored therapeutic approach. Diroximel fumarate is a second-generation fumarate with reduced gastrointestinal side effects. Moreover, several novel, selective, sphingosine-1-phosphate receptor modulators with reduced off-target effects have been developed; namely siponimod, ozanimod, and ponesimod; all oral formulations. B-cell-targeted therapies such as ocrelizumab, given intravenously, and since 2021 ofatumumab, applied subcutaneously, complement the spectrum of novel therapies. The glycoengineered antibody ublituximab is the next anti-CD20 therapy about to be approved. Within the next years, oral inhibitors of Bruton’s tyrosine kinase, currently under investigation in several phase III trials, may be licensed for multiple sclerosis. Those developments currently offer an individualized multiple sclerosis therapy, targeting patient needs with substantial effects on relapses, disability progression, and implications for daily life. In this up-to-date review, we provide a holistic overview about novel developments of the therapeutic landscape and upcoming approaches for multiple sclerosis treatment. Springer International Publishing 2022-07-22 2022 /pmc/articles/PMC9307218/ /pubmed/35869335 http://dx.doi.org/10.1007/s40263-022-00939-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review Article Faissner, Simon Gold, Ralf Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title | Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title_full | Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title_fullStr | Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title_full_unstemmed | Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title_short | Efficacy and Safety of Multiple Sclerosis Drugs Approved Since 2018 and Future Developments |
title_sort | efficacy and safety of multiple sclerosis drugs approved since 2018 and future developments |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307218/ https://www.ncbi.nlm.nih.gov/pubmed/35869335 http://dx.doi.org/10.1007/s40263-022-00939-9 |
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