欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Blitzima
适用类别Human
治疗领域Lymphoma, Non-Hodgkin;Leukemia, Lymphocytic, Chronic, B-Cell
通用名/非专利名称rituximab
活性成分rituximab
产品号EMEA/H/C/004723
患者安全信息No
许可状态Authorised
ATC编码L01FA01
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药Yes
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2017/07/13
上市许可开发者/申请人/持有人Celltrion Healthcare Hungary Kft.
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2017/05/18
欧盟委员会决定日期2025/09/25
修订号24
治疗适应症Blitzima is indicated in adults for the following indications: Non-Hodgkin’s lymphoma (NHL) Blitzima is indicated for the treatment of previously untreated patients with stage III-IV follicular lymphoma in combination with chemotherapy. Blitzima maintenance therapy is indicated for the treatment of follicular lymphoma patients responding to induction therapy. Blitzima monotherapy is indicated for treatment of patients with stage III-IV follicular lymphoma who are chemo-resistant or are in their second or subsequent relapse after chemotherapy. Blitzima is indicated for the treatment of patients with CD20 positive diffuse large B cell non-Hodgkin’s lymphoma in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy. Chronic lymphocytic leukaemia (CLL) Blitzima in combination with chemotherapy is indicated for the treatment of patients with previously untreated and relapsed/refractory CLL. Only limited data are available on efficacy and safety for patients previously treated with monoclonal antibodies including Blitzima or patients refractory to previous Blitzima plus chemotherapy.
适用物种
兽用药物ATC编码
首次发布日期2018/05/17
最后更新日期2025/09/29
产品说明书https://www.ema.europa.eu/en/documents/product-information/blitzima-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/blitzima
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