欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Orserdu
适用类别Human
治疗领域Breast Neoplasms
通用名/非专利名称elacestrant
活性成分elacestrant
产品号EMEA/H/C/005898
患者安全信息No
许可状态Authorised
ATC编码L02BA
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2023/09/15
上市许可开发者/申请人/持有人Stemline Therapeutics B.V.
人用药物治疗学分组Endocrine therapy
兽用药物治疗学分组
审评意见日期2023/07/20
欧盟委员会决定日期2025/10/13
修订号4
治疗适应症Orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (ER) positive, HER2-negative, locally advanced or metastatic breast cancer with an activating ESR1 mutation who have disease progression following at least one line of endocrine therapy including a CDK 4/6 inhibitor.
适用物种
兽用药物ATC编码
首次发布日期2023/07/18
最后更新日期2025/10/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/orserdu-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/orserdu
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