欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Yargesa
适用类别Human
治疗领域Gaucher Disease
通用名/非专利名称miglustat
活性成分miglustat
产品号EMEA/H/C/004016
患者安全信息No
许可状态Authorised
ATC编码A16AX06
是否额外监管No
是否仿制药或hybrid药物Yes
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2017/03/22
上市许可开发者/申请人/持有人Piramal Critical Care B.V.
人用药物治疗学分组Other alimentary tract and metabolism products
兽用药物治疗学分组
审评意见日期2017/01/26
欧盟委员会决定日期2023/02/17
修订号5
治疗适应症Yargesa is indicated for the oral treatment of adult patients with mild to moderate type 1 Gaucher disease. Yargesa may be used only in the treatment of patients for whom enzyme replacement therapy is unsuitable. Yargesa is indicated for the treatment of progressive neurological manifestations in adult patients and paediatric patients with Niemann-Pick type C disease.
适用物种
兽用药物ATC编码
首次发布日期2017/05/10
最后更新日期2024/02/29
产品说明书https://www.ema.europa.eu/en/documents/product-information/yargesa-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/yargesa
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase