欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Elahere
适用类别Human
治疗领域Ovarian Neoplasms;Fallopian Tube Neoplasms;Peritoneal Neoplasms
通用名/非专利名称mirvetuximab soravtansine
活性成分mirvetuximab soravtansine
产品号EMEA/H/C/005036
患者安全信息No
许可状态Authorised
ATC编码L01FX26
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Yes
上市许可日期2024/11/14
上市许可开发者/申请人/持有人AbbVie Deutschland GmbH & Co. KG
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2024/09/19
欧盟委员会决定日期2025/08/20
修订号1
治疗适应症Elahere as monotherapy is indicated for the treatment of adult patients with folate receptor-alpha (FRα) positive, platinum-resistant high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens.
适用物种
兽用药物ATC编码
首次发布日期2024/09/20
最后更新日期2025/10/02
产品说明书https://www.ema.europa.eu/en/documents/product-information/elahere-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/elahere
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