欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Yselty
适用类别Human
治疗领域Leiomyoma
通用名/非专利名称linzagolix choline
活性成分linzagolix choline
产品号EMEA/H/C/005442
患者安全信息No
许可状态Authorised
ATC编码H01CC04
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2022/06/14
上市许可开发者/申请人/持有人Theramex Ireland Limited
人用药物治疗学分组Pituitary and hypothalamic hormones and analogues
兽用药物治疗学分组
审评意见日期2021/12/16
欧盟委员会决定日期2024/11/22
修订号6
治疗适应症Yselty is indicated in adult women of reproductive age for: -           treatment of moderate to severe symptoms of uterine fibroids,-           symptomatic treatment of endometriosis in women with a history of previous medical or surgical treatment for their endometriosis (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2021/12/14
最后更新日期2025/11/21
产品说明书https://www.ema.europa.eu/en/documents/product-information/yselty-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/yselty
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