Investigational drugs in development to prevent neuromyelitis optica relapses

被引:38
|
作者
Paul, Friedemann [1 ,2 ,3 ,4 ,5 ]
Murphy, Olwen [6 ]
Pardo, Santiago [6 ]
Levy, Michael [6 ]
机构
[1] Charite, Berlin, Germany
[2] Free Univ Berlin, Berlin, Germany
[3] Humboldt Univ, Berlin, Germany
[4] NeuroCure Clin Res Ctr, Berlin Inst Hlth, Berlin, Germany
[5] Charite, Expt & Clin Res Ctr, Max Delbruck Ctr Mol Med, Berlin, Germany
[6] Johns Hopkins Univ, Dept Neurol, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
Neuromyelitis optica; biomarkers; prognosis; risk assessment; RESTORING IMMUNE TOLERANCE; VISUAL-SYSTEM DAMAGE; SPECTRUM DISORDERS; MOG-IGG; DIAGNOSTIC-CRITERIA; CLINICAL-FEATURES; MULTICENTER; EFFICACY; NMO; ECULIZUMAB;
D O I
10.1080/13543784.2018.1443077
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: In the short time since 2014, three pivotal, worldwide studies in neuromyelitis optica spectrum disorders have been launched: eculizumab, SA237 and inebelizumab, each based on a unique mechanism.Areas covered: In this review, we provide a discussion on the trial data available for each drug, a brief description of the trial design, and our expert opinion on the potential benefits and risks.Expert opinion: Eculizumab, a C5 complement inhibitor, may prove useful in the treatment of intractable cases of NMOSD, but physicians must be aware of the known risk of meningococcal infection. SA237, an interleukin-6 receptor blocker, may be effective at reducing relapse risk, and also has the potential to reduce neuropathic pain in NMOSD. Inebelizumab, a B cell depleting agent, has never been tested in NMOSD, but based on extensive evidence of efficacy with B cell depletion using rituximab, inebelizumab is expected to work at least as well.
引用
收藏
页码:265 / 271
页数:7
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