欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Sorafenib Accord
适用类别Human
治疗领域Carcinoma, Hepatocellular;Carcinoma, Renal Cell
通用名/非专利名称sorafenib
活性成分sorafenib tosilate
产品号EMEA/H/C/005921
患者安全信息No
许可状态Authorised
ATC编码L01EX02
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2022/11/09
上市许可开发者/申请人/持有人Accord Healthcare S.L.U.
人用药物治疗学分组Antineoplastic agents
兽用药物治疗学分组
审评意见日期2022/09/15
欧盟委员会决定日期2025/06/27
修订号4
治疗适应症Hepatocellular carcinomaSorafenib Accord is indicated for the treatment of hepatocellular carcinoma (see section 5.1). Renal cell carcinomaSorafenib Accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.
适用物种
兽用药物ATC编码
首次发布日期2022/09/14
最后更新日期2025/09/30
产品说明书https://www.ema.europa.eu/en/documents/product-information/sorafenib-accord-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/sorafenib-accord
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase