欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Livtencity
适用类别Human
治疗领域Cytomegalovirus Infections
通用名/非专利名称maribavir
活性成分Maribavir
产品号EMEA/H/C/005787
患者安全信息No
许可状态Authorised
ATC编码J05AX10
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2022/11/09
上市许可开发者/申请人/持有人Takeda Pharmaceuticals International AG Ireland Branch
人用药物治疗学分组Antivirals for systemic use
兽用药物治疗学分组
审评意见日期2022/09/15
欧盟委员会决定日期2025/05/15
修订号7
治疗适应症LIVTENCITY is indicated for the treatment of cytomegalovirus (CMV) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (HSCT) or solid organ transplant (SOT). Consideration should be given to official guidance on the appropriate use of antiviral agents.
适用物种
兽用药物ATC编码
首次发布日期2022/09/14
最后更新日期2025/10/22
产品说明书https://www.ema.europa.eu/en/documents/product-information/livtencity-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/livtencity
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