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Oral Disease-Modifying Therapies for Multiple Sclerosis
Classical multiple sclerosis (MS) treatments using first-line injectable drugs, although widely applied, remain a major concern in terms of therapeutic adherence and efficacy. New oral drugs recently approved for MS treatment represent significant advances in therapy. The oral route of administratio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302185/ https://www.ncbi.nlm.nih.gov/pubmed/25628732 http://dx.doi.org/10.3988/jcn.2015.11.1.9 |
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author | Kim, Woojun Zandoná, Manuella Edler Kim, Su-Hyun Kim, Ho Jin |
author_facet | Kim, Woojun Zandoná, Manuella Edler Kim, Su-Hyun Kim, Ho Jin |
author_sort | Kim, Woojun |
collection | PubMed |
description | Classical multiple sclerosis (MS) treatments using first-line injectable drugs, although widely applied, remain a major concern in terms of therapeutic adherence and efficacy. New oral drugs recently approved for MS treatment represent significant advances in therapy. The oral route of administration clearly promotes patient satisfaction and increases therapeutic compliance. However, these drugs may also have safety and tolerability issues, and a thorough analysis of the risks and benefits is required. Three oral drugs have been approved by regulatory agencies for MS treatment: fingolimod, teriflunomide, and dimethyl fumarate. This article reviews the mechanisms of action, safety, and efficacy of these drugs and two other drugs that have yielded positive results in phase III trials: cladribine and laquinimod. |
format | Online Article Text |
id | pubmed-4302185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Neurological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-43021852015-01-27 Oral Disease-Modifying Therapies for Multiple Sclerosis Kim, Woojun Zandoná, Manuella Edler Kim, Su-Hyun Kim, Ho Jin J Clin Neurol Review Classical multiple sclerosis (MS) treatments using first-line injectable drugs, although widely applied, remain a major concern in terms of therapeutic adherence and efficacy. New oral drugs recently approved for MS treatment represent significant advances in therapy. The oral route of administration clearly promotes patient satisfaction and increases therapeutic compliance. However, these drugs may also have safety and tolerability issues, and a thorough analysis of the risks and benefits is required. Three oral drugs have been approved by regulatory agencies for MS treatment: fingolimod, teriflunomide, and dimethyl fumarate. This article reviews the mechanisms of action, safety, and efficacy of these drugs and two other drugs that have yielded positive results in phase III trials: cladribine and laquinimod. Korean Neurological Association 2015-01 2015-01-02 /pmc/articles/PMC4302185/ /pubmed/25628732 http://dx.doi.org/10.3988/jcn.2015.11.1.9 Text en Copyright © 2015 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Kim, Woojun Zandoná, Manuella Edler Kim, Su-Hyun Kim, Ho Jin Oral Disease-Modifying Therapies for Multiple Sclerosis |
title | Oral Disease-Modifying Therapies for Multiple Sclerosis |
title_full | Oral Disease-Modifying Therapies for Multiple Sclerosis |
title_fullStr | Oral Disease-Modifying Therapies for Multiple Sclerosis |
title_full_unstemmed | Oral Disease-Modifying Therapies for Multiple Sclerosis |
title_short | Oral Disease-Modifying Therapies for Multiple Sclerosis |
title_sort | oral disease-modifying therapies for multiple sclerosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302185/ https://www.ncbi.nlm.nih.gov/pubmed/25628732 http://dx.doi.org/10.3988/jcn.2015.11.1.9 |
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