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Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects

Multiple sclerosis (MS) is a prevalent and debilitating neurologic condition characterized by widespread neurodegeneration and the formation of focal demyelinating plaques in the central nervous system. Current therapeutic options are complex and attempt to manage acute relapse, modify disease, and...

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Autores principales: Lassiter, Grace, Melancon, Carlie, Rooney, Tyler, Murat, Anne-Marie, Kaye, Jessica S., Kaye, Adam M., Kaye, Rachel J., Cornett, Elyse M., Kaye, Alan D., Shah, Rutvij J., Viswanath, Omar, Urits, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768354/
https://www.ncbi.nlm.nih.gov/pubmed/33287177
http://dx.doi.org/10.3390/neurolint12030016
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author Lassiter, Grace
Melancon, Carlie
Rooney, Tyler
Murat, Anne-Marie
Kaye, Jessica S.
Kaye, Adam M.
Kaye, Rachel J.
Cornett, Elyse M.
Kaye, Alan D.
Shah, Rutvij J.
Viswanath, Omar
Urits, Ivan
author_facet Lassiter, Grace
Melancon, Carlie
Rooney, Tyler
Murat, Anne-Marie
Kaye, Jessica S.
Kaye, Adam M.
Kaye, Rachel J.
Cornett, Elyse M.
Kaye, Alan D.
Shah, Rutvij J.
Viswanath, Omar
Urits, Ivan
author_sort Lassiter, Grace
collection PubMed
description Multiple sclerosis (MS) is a prevalent and debilitating neurologic condition characterized by widespread neurodegeneration and the formation of focal demyelinating plaques in the central nervous system. Current therapeutic options are complex and attempt to manage acute relapse, modify disease, and manage symptoms. Such therapies often prove insufficient alone and highlight the need for more targeted MS treatments with reduced systemic side effect profiles. Ozanimod is a novel S1P (sphingosine-1-phosphate) receptor modulator used for the treatment of clinically isolated syndrome, relapsing–remitting, and secondary progressive forms of multiple sclerosis. It selectively modulates S1P1 and S1P5 receptors to prevent autoreactive lymphocytes from entering the CNS where they can promote nerve damage and inflammation. Ozanimod was approved by the US Food and Drug Administration (US FDA) for the management of multiple sclerosis in March 2020 and has been proved to be both effective and well tolerated. Of note, ozanimod is associated with the following complications: increased risk of infections, liver injury, fetal risk, increased blood pressure, respiratory effects, macular edema, and posterior reversible encephalopathy syndrome, among others. Further investigation including head-to-head clinical trials is warranted to evaluate the efficacy of ozanimod compared with other S1P1 receptor modulators.
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spelling pubmed-77683542020-12-29 Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects Lassiter, Grace Melancon, Carlie Rooney, Tyler Murat, Anne-Marie Kaye, Jessica S. Kaye, Adam M. Kaye, Rachel J. Cornett, Elyse M. Kaye, Alan D. Shah, Rutvij J. Viswanath, Omar Urits, Ivan Neurol Int Review Multiple sclerosis (MS) is a prevalent and debilitating neurologic condition characterized by widespread neurodegeneration and the formation of focal demyelinating plaques in the central nervous system. Current therapeutic options are complex and attempt to manage acute relapse, modify disease, and manage symptoms. Such therapies often prove insufficient alone and highlight the need for more targeted MS treatments with reduced systemic side effect profiles. Ozanimod is a novel S1P (sphingosine-1-phosphate) receptor modulator used for the treatment of clinically isolated syndrome, relapsing–remitting, and secondary progressive forms of multiple sclerosis. It selectively modulates S1P1 and S1P5 receptors to prevent autoreactive lymphocytes from entering the CNS where they can promote nerve damage and inflammation. Ozanimod was approved by the US Food and Drug Administration (US FDA) for the management of multiple sclerosis in March 2020 and has been proved to be both effective and well tolerated. Of note, ozanimod is associated with the following complications: increased risk of infections, liver injury, fetal risk, increased blood pressure, respiratory effects, macular edema, and posterior reversible encephalopathy syndrome, among others. Further investigation including head-to-head clinical trials is warranted to evaluate the efficacy of ozanimod compared with other S1P1 receptor modulators. MDPI 2020-12-03 /pmc/articles/PMC7768354/ /pubmed/33287177 http://dx.doi.org/10.3390/neurolint12030016 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lassiter, Grace
Melancon, Carlie
Rooney, Tyler
Murat, Anne-Marie
Kaye, Jessica S.
Kaye, Adam M.
Kaye, Rachel J.
Cornett, Elyse M.
Kaye, Alan D.
Shah, Rutvij J.
Viswanath, Omar
Urits, Ivan
Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title_full Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title_fullStr Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title_full_unstemmed Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title_short Ozanimod to Treat Relapsing Forms of Multiple Sclerosis: A Comprehensive Review of Disease, Drug Efficacy and Side Effects
title_sort ozanimod to treat relapsing forms of multiple sclerosis: a comprehensive review of disease, drug efficacy and side effects
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768354/
https://www.ncbi.nlm.nih.gov/pubmed/33287177
http://dx.doi.org/10.3390/neurolint12030016
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