欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Rozlytrek
适用类别Human
治疗领域Cancer;Carcinoma, Non-Small-Cell Lung
通用名/非专利名称entrectinib
活性成分Entrectinib
产品号EMEA/H/C/004936
患者安全信息No
许可状态Authorised
ATC编码L01EX14
是否额外监管Yes
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2020/07/31
上市许可开发者/申请人/持有人Roche Registration 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2020/05/28
欧盟委员会决定日期2025/03/24
修订号11
治疗适应症Rozlytrek as monotherapy is indicated for the treatment of adult and paediatric patients 12 years of age and older with solid tumours expressing a neurotrophic tyrosine receptor kinase (NTRK) gene fusion, who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, and who have not received a prior NTRK inhibitor who have no satisfactory treatment options. Rozlytrek as monotherapy is indicated for the treatment of adult patients with ROS1 positive, advanced non small cell lung cancer (NSCLC) not previously treated with ROS1 inhibitors.
适用物种
兽用药物ATC编码
首次发布日期2020/09/11
最后更新日期2025/06/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/rozlytrek-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/rozlytrek
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