欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tremelimumab AstraZeneca
适用类别Human
治疗领域Carcinoma, Non-Small-Cell Lung
通用名/非专利名称tremelimumab
活性成分Tremelimumab
产品号EMEA/H/C/004650
患者安全信息no
授权状态Authorised
ATC编码L01FX20
是否额外监管yes
是否仿制药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
批准上市日期2023/02/20
上市许可持有人/公司名称AstraZeneca AB
人用药物治疗分组Antineoplastic agents
审评意见发布日期2022/12/15
决定日期2023/09/04
修订号1
适应症Tremelimumab AstraZeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (NSCLC) with no sensitising EGFR mutations or ALK positive mutations.
首次发布日期2022/12/09
修订日期2023/09/11
产品信息https://www.ema.europa.eu/en/documents/product-information/tremelimumab-astrazeneca-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tremelimumab-astrazeneca
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