欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Kerendia
适用类别Human
治疗领域Renal Insufficiency, Chronic;Diabetes Mellitus, Type 2;Heart Failure
通用名/非专利名称finerenone
活性成分finerenone
产品号EMEA/H/C/005200
患者安全信息No
许可状态Authorised
ATC编码C09
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2022/02/16
上市许可开发者/申请人/持有人Bayer AG
人用药物治疗学分组Agents acting on the renin-angiotensin system
兽用药物治疗学分组
审评意见日期2021/12/16
欧盟委员会决定日期2026/03/26
修订号4
治疗适应症Kerendia is indicated for the treatment of chronic kidney disease (with albuminuria) associated with type 2 diabetes in adults. For study results with respect to renal and cardiovascular events, see section 5.1. Kerendia is indicated for the treatment of symptomatic chronic heart failure with left ventricular ejection fraction (LVEF) ≥ 40% in adults.
适用物种
兽用药物ATC编码
首次发布日期2021/12/14
最后更新日期2026/05/07
产品说明书https://www.ema.europa.eu/en/documents/product-information/kerendia-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/kerendia
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