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Zilucoplan:一种在研的补体 C5 抑制剂,用于治疗乙酰胆碱受体自身抗体阳性的全身性重症肌无力。

Zilucoplan: An Investigational Complement C5 Inhibitor for the Treatment of Acetylcholine Receptor Autoantibody-Positive Generalized Myasthenia Gravis.

机构信息

Department of Neurology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.

Department of Clinical Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

出版信息

Expert Opin Investig Drugs. 2021 May;30(5):483-493. doi: 10.1080/13543784.2021.1897567. Epub 2021 Apr 1.

DOI:10.1080/13543784.2021.1897567
PMID:33792453
Abstract

INTRODUCTION

Generalized myasthenia gravis (gMG) is an autoimmune disorder in which pathogenic autoantibodies damage the neuromuscular junction, causing disabling or life-threatening muscle weakness. Most treatments nonspecifically inhibit aspects of the immune system, do not directly address the causal mechanisms of tissue damage, and often have side-effect profiles that negatively impact patients. Understanding of the central pathogenic role of the complement cascade in gMG is advancing, and a new complement-targeting treatment is under investigation.

AREAS COVERED

We provide an overview of gMG etiology, the complement cascade, current treatments, and the investigational gMG therapy zilucoplan. Zilucoplan is a small, subcutaneously administered, macrocyclic peptide that inhibits cleavage of complement component C5 and the subsequent formation of the membrane attack complex.

EXPERT OPINION

In a randomized, double-blind, placebo-controlled, phase 2 clinical trial, zilucoplan demonstrated clinically meaningful complement inhibition in patients with acetylcholine receptor-positive gMG. Zilucoplan, a first-of-its-kind cyclic peptide targeting C5, appears to be a therapeutic option for the treatment of gMG based on available pharmacokinetic/pharmacodynamic data and phase 1 and 2 efficacy, safety, and tolerability data with limited long-term follow-up. Zilucoplan use earlier in the treatment paradigm would be suitable in this population should phase 3 efficacy and safety data be equally favorable.

摘要

简介

全身性重症肌无力(gMG)是一种自身免疫性疾病,其中致病性自身抗体损害神经肌肉接头,导致使人丧失能力或危及生命的肌肉无力。大多数治疗方法是非特异性地抑制免疫系统的各个方面,不能直接针对组织损伤的因果机制,而且往往具有负面影响患者的副作用特征。人们对补体级联在 gMG 中的中心致病作用的理解正在不断深入,一种新的补体靶向治疗方法正在研究中。

涵盖的领域

我们提供 gMG 病因、补体级联、当前治疗方法以及研究性 gMG 治疗药物zilucoplan 的概述。zilucoplan 是一种小的、皮下给药的大环肽,可抑制补体成分 C5 的切割以及随后膜攻击复合物的形成。

专家意见

在一项随机、双盲、安慰剂对照、2 期临床试验中,zilucoplan 显示出在乙酰胆碱受体阳性 gMG 患者中有临床意义的补体抑制作用。zilucoplan 是一种针对 C5 的首创的环状肽,根据现有的药代动力学/药效学数据以及 1 期和 2 期的疗效、安全性和耐受性数据(具有有限的长期随访),它似乎是治疗 gMG 的一种治疗选择。在这一人群中,如果 3 期疗效和安全性数据同样有利,早期在治疗方案中使用 zilucoplan 将是合适的。

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