欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Leqembi
适用类别Human
治疗领域Cognitive Dysfunction;Alzheimer Disease
通用名/非专利名称Lecanemab
活性成分Lecanemab
产品号EMEA/H/C/005966
患者安全信息No
许可状态Authorised
ATC编码N06DX04
是否额外监管Yes
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2025/04/15
上市许可开发者/申请人/持有人Eisai GmbH
人用药物治疗学分组Psychoanaleptics
兽用药物治疗学分组
审评意见日期2024/11/14
修订号
治疗适应症Leqembi is indicated for the treatment of adult patients with a clinical diagnosis of mild cognitive impairment and mild dementia due to Alzheimer’s disease (Early Alzheimer’s disease) who are apolipoprotein E 4 (ApoE ε4) non-carriers or heterozygotes with confirmed amyloid pathology (see section 4.4).
适用物种
兽用药物ATC编码
首次发布日期2025/02/28
最后更新日期2025/05/05
产品说明书https://www.ema.europa.eu/en/documents/product-information/leqembi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/leqembi
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