欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Azacitidine Kabi
适用类别Human
治疗领域Myelodysplastic Syndromes;Leukemia, Myelomonocytic, Chronic;Leukemia, Myeloid, Acute
通用名/非专利名称azacitidine
活性成分azacitidine
产品号EMEA/H/C/006154
患者安全信息No
许可状态Authorised
ATC编码L01BC07
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2024/01/05
上市许可开发者/申请人/持有人Fresenius Kabi Deutschland GmbH
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2023/11/10
欧盟委员会决定日期2024/08/29
修订号1
治疗适应症Azacitidine Kabi is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation(HSCT) with: Intermediate-2 and high-risk myelodysplastic syndromes (MDS) according to the international prognostic scoring system (IPSS), Chronic myelomonocytic leukaemia (CMML) with 10-29% marrow blasts without myeloproliferative disorder, Acute myeloid leukaemia (AML) with 20-30% blasts and multi-lineage dysplasia, according to World Health Organization (WHO) classification, AML with > 30% marrow blasts according to the WHO classification.
适用物种
兽用药物ATC编码
首次发布日期2023/11/10
最后更新日期2024/08/30
产品说明书https://www.ema.europa.eu/en/documents/product-information/azacitidine-kabi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/azacitidine-kabi
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