医学
肾病
安慰剂
替代补体途径
双盲
发病机制
补语(音乐)
随机对照试验
内科学
免疫学
胃肠病学
补体系统
抗体
病理
内分泌学
替代医学
糖尿病
化学
互补
表型
基因
生物化学
作者
J. Barratt,B. Rovin,H. Zhang,N. Kashihara,B. Maes,D. Rizk,H. Trimarchi,B. Sprangers,M. Meier,D. Kollins,W. Wang,A. Magirr,V. Perkovic
标识
DOI:10.1016/j.ekir.2022.01.577
摘要
No approved targeted therapies currently exist for IgA nephropathy (IgAN). Targeting the alternative complement pathway (AP) is an attractive therapeutic strategy given its role in the pathogenesis of IgAN. Iptacopan (LNP023) is a first-in-class, oral, potent and highly selective inhibitor of factor B of AP.
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