Siponimod—A Selective Sphingosine-1-phosphate Modulator for Secondary Progressive Multiple Sclerosis

J. Thornton, A. Harel
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引用次数: 0

Abstract

Over the past decade, there has been a rapid expansion of disease-modifying therapies for multiple sclerosis (MS), which exhibit a variety of different mechanisms of action. While the non-selective sphingosine-1-phosphate (S1P) receptor modulator fingolimod has been available for a decade, two novel selective S1P receptor modulators, siponimod and ozanimod, have been recently approved by the US Food and Drug Adminstration for use in "active" secondary progressive MS (SPMS). Siponimod, the subject of this article, is the only S1P receptor modulator studied in both relapsing remitting MS and SPMS. In this article, we review the clinical trial data regarding use of this medication and the implications for use in patients with SPMS.
siponimoda选择性鞘氨醇-1-磷酸调节剂治疗继发性进行性多发性硬化
在过去的十年中,多发性硬化症(MS)的疾病改善疗法迅速扩大,这些疗法表现出多种不同的作用机制。虽然非选择性鞘氨醇-1-磷酸(S1P)受体调节剂fingolimod已上市10年,但两种新的选择性S1P受体调节剂siponimod和ozanimod最近已被美国食品和药物管理局批准用于“主动”继发性进展性多发性硬化症(SPMS)。Siponimod,这篇文章的主题,是唯一的S1P受体调节剂研究复发缓解型MS和SPMS。在这篇文章中,我们回顾了关于使用这种药物的临床试验数据以及对SPMS患者使用的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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