The Immune Regulator NLRX1 Limits Inflammatory Neurodegeneration in the Anterior Visual Pathway

common TEAE (71.1% vs 71.6%, respectively).In the prior-rituximabtreated group, no deaths occurred; no patients experienced TEAEs/ TESAEs leading to C5IT withdrawal.There were no differences in TEAE/TESAE incidence rates when analyzed by time since last rituximab use. ConclusionsNo differences in safety were observed among prior-rituximab-treated patients in the PREVENT and CHAMPION-NMOSD studies.These findings provide important information to guide clinical decisionmaking when considering a switch from rituximab to C5IT in patients with AQP4-Ab+ NMOSD who received rituximab within the preceding 3-12 months.Study Supported By: Alexion, AstraZeneca Rare Disease.Disclosure: Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Mitsubishi Pharma.Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a

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Publication Details

Journal
Neurology
Published
2024-10-08
DOI
https://doi.org/10.1212/01.wnl.0001051492.92479.e3
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

The Immune Regulator NLRX1 Limits Inflammatory Neurodegeneration in the Anterior Visual Pathway

Marjan Gharagozloo, Danny Galleguillos, Thomas Garton, Matthew D. Smith et al.
Neurology
Neuroinflammation and Neurodegeneration Mechanisms
article

The Immune Regulator NLRX1 Limits Inflammatory Neurodegeneration in the Anterior Visual Pathway

Marjan Gharagozloo, Danny Galleguillos, Thomas Garton, Matthew D. Smith, Peter A. Calabresi, Alexander Gill
article en

Abstract

common TEAE (71.1% vs 71.6%, respectively).In the prior-rituximabtreated group, no deaths occurred; no patients experienced TEAEs/ TESAEs leading to C5IT withdrawal.There were no differences in TEAE/TESAE incidence rates when analyzed by time since last rituximab use. ConclusionsNo differences in safety were observed among prior-rituximab-treated patients in the PREVENT and CHAMPION-NMOSD studies.These findings provide important information to guide clinical decisionmaking when considering a switch from rituximab to C5IT in patients with AQP4-Ab+ NMOSD who received rituximab within the preceding 3-12 months.Study Supported By: Alexion, AstraZeneca Rare Disease.Disclosure: Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Mitsubishi Pharma.Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a

NeurologyVol. 103(7_Supplement_1)
AstraZeneca, Sanofi, Biogen, Alexion Pharmaceuticals, Regeneron Pharmaceuticals, National Institutes of Health, National Cancer Institute
Zero hunger
Openalex Percentile: Top 81%
Neuroinflammation and Neurodegeneration Mechanisms
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