欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Mepact
适用类别Human
治疗领域Osteosarcoma
通用名/非专利名称mifamurtide
活性成分mifamurtide
产品号EMEA/H/C/000802
患者安全信息No
许可状态Authorised
ATC编码L03AX15
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2009/03/06
上市许可开发者/申请人/持有人Esteve Pharmaceuticals, S.A.
人用药物治疗学分组Immunostimulants
兽用药物治疗学分组
欧盟委员会决定日期2025/12/18
修订号22
治疗适应症Mepact is indicated in children, adolescents and young adults for the treatment of high-grade resectable non-metastatic osteosarcoma after macroscopically complete surgical resection. It is used in combination with postoperative multi-agent chemotherapy. Safety and efficacy have been assessed in studies of patients two to 30 years of age at initial diagnosis.
适用物种
兽用药物ATC编码
首次发布日期2016/12/14
最后更新日期2025/12/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/mepact-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/mepact
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