欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Idefirix
适用类别Human
治疗领域Desensitization, Immunologic;Kidney Transplantation
通用名/非专利名称imlifidase
活性成分imlifidase
产品号EMEA/H/C/004849
患者安全信息No
许可状态Authorised
ATC编码L04AA
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Yes
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2020/08/25
上市许可开发者/申请人/持有人Hansa Biopharma AB
人用药物治疗学分组Immunosuppressants
兽用药物治疗学分组
审评意见日期2020/06/25
欧盟委员会决定日期2025/06/25
修订号8
治疗适应症Idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. The use of Idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.
适用物种
兽用药物ATC编码
首次发布日期2020/08/28
最后更新日期2025/07/02
产品说明书https://www.ema.europa.eu/en/documents/product-information/idefirix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/idefirix
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase