欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Sutent
适用类别Human
治疗领域Gastrointestinal Stromal Tumors;Carcinoma, Renal Cell;Neuroendocrine Tumors
通用名/非专利名称sunitinib
活性成分sunitinib
产品号EMEA/H/C/000687
患者安全信息No
许可状态Authorised
ATC编码L01EX01
是否额外监管No
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2006/07/19
上市许可开发者/申请人/持有人Pfizer Limited
人用药物治疗学分组Antineoplastic agents
兽用药物治疗学分组
欧盟委员会决定日期2025/03/10
修订号41
治疗适应症Gastrointestinal stromal tumour (GIST) Sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (GIST) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. Metastatic renal cell carcinoma (MRCC) Sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (MRCC) in adults. Pancreatic neuroendocrine tumours (pNET) Sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. Experience with Sutent as first-line treatment is limited (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2018/02/22
最后更新日期2025/03/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/sutent-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/sutent
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase