Back to Search Start Over

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

Authors :
Lassiter G
Melancon C
Rooney T
Murat AM
Kaye JS
Kaye AM
Kaye RJ
Cornett EM
Kaye AD
Shah RJ
Viswanath O
Urits I
Source :
Neurology international [Neurol Int] 2020 Dec 03; Vol. 12 (3), pp. 89-108. Date of Electronic Publication: 2020 Dec 03.
Publication Year :
2020

Abstract

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.

Details

Language :
English
ISSN :
2035-8385
Volume :
12
Issue :
3
Database :
MEDLINE
Journal :
Neurology international
Publication Type :
Academic Journal
Accession number :
33287177
Full Text :
https://doi.org/10.3390/neurolint12030016