欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tepadina
适用类别Human
治疗领域Hematopoietic Stem Cell Transplantation
通用名/非专利名称thiotepa
活性成分thiotepa
产品号EMEA/H/C/001046
患者安全信息No
许可状态Authorised
ATC编码L01AC01
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2010/03/15
上市许可开发者/申请人/持有人ADIENNE S.r.l. S.U.
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2009/12/17
欧盟委员会决定日期2025/07/24
修订号23
治疗适应症TEPADINA is indicated, in combination with other chemotherapy medicinal products:- with or without total body irradiation (TBI), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (HPCT) in haematological diseases in adult and paediatric patients;- when high dose chemotherapy with HPCT support is appropriate for the treatment of solid tumours in adult and paediatric patients.
适用物种
兽用药物ATC编码
首次发布日期2017/11/29
最后更新日期2025/10/07
产品说明书https://www.ema.europa.eu/en/documents/product-information/tepadina-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tepadina
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