欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Ivozall
适用类别Human
治疗领域Precursor Cell Lymphoblastic Leukemia-Lymphoma
通用名/非专利名称clofarabine
活性成分clofarabine
产品号EMEA/H/C/005039
患者安全信息No
许可状态Withdrawn
ATC编码L01BB06
是否额外监管No
是否仿制药或hybrid药物Yes
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2019/11/14
上市许可开发者/申请人/持有人ORPHELIA Pharma
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2019/09/19
欧盟委员会决定日期2023/03/06
修订号5
治疗适应症Treatment of acute lymphoblastic leukaemia (ALL) in paediatric patients who have relapsed or are refractory after receiving at least two prior regimens and where there is no other treatment option anticipated to result in a durable response. Safety and efficacy have been assessed in studies of patients ? 21 years old at initial diagnosis.
适用物种
兽用药物ATC编码
首次发布日期2019/11/22
最后更新日期2023/12/07
产品说明书https://www.ema.europa.eu/en/documents/product-information/ivozall-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/ivozall
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