欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Zalmoxis
适用类别Human
治疗领域Hematopoietic Stem Cell Transplantation;Graft vs Host Disease
通用名/非专利名称allogeneic T cells genetically modified with a retroviral vector encoding for a truncated form of the human low affinity nerve growth factor receptor (ΔLNGFR) and the herpes simplex I virus thymidine kinase (HSV-TK Mut2)
活性成分allogeneic T cells genetically modified with a retroviral vector encoding for a truncated form of the human low affinity nerve growth factor receptor (ΔLNGFR) and the herpes simplex I virus thymidine kinase (HSV-TK Mut2)
产品号EMEA/H/C/002801
患者安全信息No
许可状态Withdrawn
ATC编码L01
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2016/08/18
上市许可开发者/申请人/持有人MolMed SpA
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2016/06/23
欧盟委员会决定日期2018/07/26
修订号1
治疗适应症Zalmoxis is indicated as adjunctive treatment in haploidentical haematopoietic stem cell transplantation (HSCT) of adult patients with high-risk haematological malignancies.
适用物种
兽用药物ATC编码
首次发布日期2018/07/26
最后更新日期2020/02/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/zalmoxis-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/zalmoxis
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