耐受性
医学
多神经根神经病
弱点
安慰剂
多灶性运动神经病
不利影响
内科学
外科
免疫学
替代医学
失配负性
脑电图
格林-巴利综合征
病理
精神科
作者
Jeffrey A. Allen,Jie Lin,Ivana Basta,Tina Dysgaard,Christian Eggers,Jeffrey T. Guptill,Kelly Gwathmey,Channa Hewamadduma,Erik Hofman,Yessar Hussain,Satoshi Kuwabara,Gwendal Le Masson,Frank Leypoldt,Ting Chang,Marta Lipowska,Murray Lowe,Giuseppe Lauria,Luís Querol,Mihaela-Adriana Simu,Niraja Suresh
出处
期刊:Lancet Neurology
[Elsevier BV]
日期:2024-09-19
卷期号:23 (10): 1013-1024
被引量:11
标识
DOI:10.1016/s1474-4422(24)00309-0
摘要
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an autoimmune disease of the peripheral nervous system that can lead to severe disability from muscle weakness and sensory disturbances. Around a third of patients do not respond to currently available treatments, and many patients with a partial response have residual neurological impairment, highlighting the need for effective alternatives. Efgartigimod alfa, a human IgG1 antibody Fc fragment, has demonstrated efficacy and safety in patients with generalised myasthenia gravis. We evaluated the safety, tolerability, and efficacy of subcutaneous efgartigimod PH20 in adults with CIDP.
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