重症肌无力
医学
安慰剂
受体
重组DNA
抗体
免疫学
内科学
病理
替代医学
生物化学
基因
化学
标识
DOI:10.1038/s41582-021-00547-z
摘要
A randomized, placebo-controlled trial has found the neonatal Fc receptor modulator efgartigimod to be an effective therapy for generalized myasthenia gravis. If a pending FDA application is approved, the treatment will be the first recombinant antibody-based therapy for selective IgG depletion, adding to a growing spectrum of treatment options for myasthenia gravis.
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