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Novel Drugs in a Pipeline for Progressive Multiple Sclerosis

Multiple sclerosis (MS) is a widely known inflammatory, demyelinating disease of the central nervous system. The pathogenesis of progressive multiple sclerosis (PMS) is a complex, multi-level process that causes therapeutic difficulties. Along with variables such as age and duration of the disease,...

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Autores principales: Sapko, Klaudia, Jamroz-Wiśniewska, Anna, Rejdak, Konrad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225445/
https://www.ncbi.nlm.nih.gov/pubmed/35743410
http://dx.doi.org/10.3390/jcm11123342
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author Sapko, Klaudia
Jamroz-Wiśniewska, Anna
Rejdak, Konrad
author_facet Sapko, Klaudia
Jamroz-Wiśniewska, Anna
Rejdak, Konrad
author_sort Sapko, Klaudia
collection PubMed
description Multiple sclerosis (MS) is a widely known inflammatory, demyelinating disease of the central nervous system. The pathogenesis of progressive multiple sclerosis (PMS) is a complex, multi-level process that causes therapeutic difficulties. Along with variables such as age and duration of the disease, pathogenetic mechanisms change from inflammatory to neurodegenerative processes. Therefore, the efficacy of available anti-inflammatory drugs approved for the treatment of PMS, such as ocrelizumab or siponimod, is limited in time. In search of innovative solutions, several research studies have been conducted to evaluate the effectiveness of drugs with neuroprotective or remyelinating effects in PMS, including biotin, ibudilast, simvastatin, alpha-lipoic acid, clemastine, amiloride, fluoxetine, riluzole, masitinib, opicinumab, and lamotrigine. The current review includes those compounds, which have entered the clinical phase of assessment, and the authors discuss future prospects for successful PMS treatment.
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spelling pubmed-92254452022-06-24 Novel Drugs in a Pipeline for Progressive Multiple Sclerosis Sapko, Klaudia Jamroz-Wiśniewska, Anna Rejdak, Konrad J Clin Med Review Multiple sclerosis (MS) is a widely known inflammatory, demyelinating disease of the central nervous system. The pathogenesis of progressive multiple sclerosis (PMS) is a complex, multi-level process that causes therapeutic difficulties. Along with variables such as age and duration of the disease, pathogenetic mechanisms change from inflammatory to neurodegenerative processes. Therefore, the efficacy of available anti-inflammatory drugs approved for the treatment of PMS, such as ocrelizumab or siponimod, is limited in time. In search of innovative solutions, several research studies have been conducted to evaluate the effectiveness of drugs with neuroprotective or remyelinating effects in PMS, including biotin, ibudilast, simvastatin, alpha-lipoic acid, clemastine, amiloride, fluoxetine, riluzole, masitinib, opicinumab, and lamotrigine. The current review includes those compounds, which have entered the clinical phase of assessment, and the authors discuss future prospects for successful PMS treatment. MDPI 2022-06-10 /pmc/articles/PMC9225445/ /pubmed/35743410 http://dx.doi.org/10.3390/jcm11123342 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sapko, Klaudia
Jamroz-Wiśniewska, Anna
Rejdak, Konrad
Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title_full Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title_fullStr Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title_full_unstemmed Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title_short Novel Drugs in a Pipeline for Progressive Multiple Sclerosis
title_sort novel drugs in a pipeline for progressive multiple sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225445/
https://www.ncbi.nlm.nih.gov/pubmed/35743410
http://dx.doi.org/10.3390/jcm11123342
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