欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Calquence
适用类别Human
治疗领域Leukemia, Lymphocytic, Chronic, B-Cell
通用名/非专利名称acalabrutinib
活性成分acalabrutinib;acalabrutinib maleate
产品号EMEA/H/C/005299
患者安全信息No
许可状态Authorised
ATC编码L01EL02
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2020/11/05
上市许可开发者/申请人/持有人AstraZeneca AB
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2020/11/05
欧盟委员会决定日期2025/08/28
修订号11
治疗适应症Calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL).Calquence in combination with venetoclax with or without obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (CLL).Calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (CLL) who have received at least one prior therapy.Calquence in combination with bendamustine and rituximab (BR) is indicated for the treatment of adult patients with previously untreated mantle cell lymphoma (MCL) who are not eligible for autologous stem cell transplant (ASCT).Calquence as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) not previously treated with a BTK inhibitor.
适用物种
兽用药物ATC编码
首次发布日期2020/11/11
最后更新日期2025/09/19
产品说明书https://www.ema.europa.eu/en/documents/product-information/calquence-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/calquence
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