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Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder
Inebilizumab (Uplizna(®)) is a recently approved monoclonal antibody for use in adults with neuromyelitis optica spectrum disorder (NMOSD) who are anti-aquaporin-4 (AQP4) antibody seropositive. Inebilizumab targets the B cell antigen CD19 and effectively depletes circulating B cells, thus suppressin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550749/ https://www.ncbi.nlm.nih.gov/pubmed/36070074 http://dx.doi.org/10.1007/s40263-022-00949-7 |
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author | Nie, Tina Blair, Hannah A. |
author_facet | Nie, Tina Blair, Hannah A. |
author_sort | Nie, Tina |
collection | PubMed |
description | Inebilizumab (Uplizna(®)) is a recently approved monoclonal antibody for use in adults with neuromyelitis optica spectrum disorder (NMOSD) who are anti-aquaporin-4 (AQP4) antibody seropositive. Inebilizumab targets the B cell antigen CD19 and effectively depletes circulating B cells, thus suppressing inflammatory NMOSD attacks that are potentially disabling or life-threatening. It is approved as an intravenous infusion in several countries. In the pivotal phase 2/3 N-MOmentum trial, inebilizumab reduced the risk of NMOSD attacks compared with placebo, including in AQP4-antibody seropositive patients. Inebilizumab also significantly reduced the risk of disability score worsening, the number of NMOSD-related hospitalisations and MRI lesion count, but had no significant effect on low-contrast binocular vision. The treatment effect on relapse risk and disability scores was sustained in inebilizumab-treated patients for ≥ 4 years during the open-label extension. Inebilizumab was generally well tolerated, with the most common adverse events being urinary tract infection and arthralgia. Thus, inebilizumab is an effective treatment option for adults with AQP4-antibody seropositive NMOSD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40263-022-00949-7. |
format | Online Article Text |
id | pubmed-9550749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-95507492022-10-12 Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder Nie, Tina Blair, Hannah A. CNS Drugs Adis Drug Evaluation Inebilizumab (Uplizna(®)) is a recently approved monoclonal antibody for use in adults with neuromyelitis optica spectrum disorder (NMOSD) who are anti-aquaporin-4 (AQP4) antibody seropositive. Inebilizumab targets the B cell antigen CD19 and effectively depletes circulating B cells, thus suppressing inflammatory NMOSD attacks that are potentially disabling or life-threatening. It is approved as an intravenous infusion in several countries. In the pivotal phase 2/3 N-MOmentum trial, inebilizumab reduced the risk of NMOSD attacks compared with placebo, including in AQP4-antibody seropositive patients. Inebilizumab also significantly reduced the risk of disability score worsening, the number of NMOSD-related hospitalisations and MRI lesion count, but had no significant effect on low-contrast binocular vision. The treatment effect on relapse risk and disability scores was sustained in inebilizumab-treated patients for ≥ 4 years during the open-label extension. Inebilizumab was generally well tolerated, with the most common adverse events being urinary tract infection and arthralgia. Thus, inebilizumab is an effective treatment option for adults with AQP4-antibody seropositive NMOSD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40263-022-00949-7. Springer International Publishing 2022-09-07 2022 /pmc/articles/PMC9550749/ /pubmed/36070074 http://dx.doi.org/10.1007/s40263-022-00949-7 Text en © Springer Nature 2022, corrected publication 2022 https://creativecommons.org/licenses/by-nc/4.0/ Open Access This 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 | Adis Drug Evaluation Nie, Tina Blair, Hannah A. Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title | Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title_full | Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title_fullStr | Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title_full_unstemmed | Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title_short | Inebilizumab: A Review in Neuromyelitis Optica Spectrum Disorder |
title_sort | inebilizumab: a review in neuromyelitis optica spectrum disorder |
topic | Adis Drug Evaluation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550749/ https://www.ncbi.nlm.nih.gov/pubmed/36070074 http://dx.doi.org/10.1007/s40263-022-00949-7 |
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