欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tepkinly
适用类别Human
治疗领域Lymphoma, Large B-Cell, Diffuse
通用名/非专利名称epcoritamab
活性成分epcoritamab
产品号EMEA/H/C/005985
患者安全信息No
许可状态Authorised
ATC编码L01FX27
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No
上市许可日期2023/09/22
上市许可开发者/申请人/持有人AbbVie Deutschland GmbH & Co. KG
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2023/07/20
欧盟委员会决定日期2025/07/17
修订号5
治疗适应症Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy.Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy.Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy.Tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy. 
适用物种
兽用药物ATC编码
首次发布日期2023/07/17
最后更新日期2025/09/19
产品说明书https://www.ema.europa.eu/en/documents/product-information/tepkinly-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tepkinly
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