欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称mCombriax
适用类别Human
治疗领域Influenza, Human;COVID-19 virus infection
通用名/非专利名称influenza mRNA vaccine;COVID-19 mRNA vaccine
活性成分single-stranded, 5’-capped messenger RNAs (mRNAs) produced using a cell-free in vitro transcription from the corresponding DNA template, encoding seasonal influenza haemagglutinin (HA) glycoproteins: A/H1N1, A/H3N2, B/Victoria
产品号EMEA/H/C/006472
患者安全信息No
许可状态Authorised
ATC编码J07B
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2026/04/20
上市许可开发者/申请人/持有人Moderna Biotech Spain, S.L.
人用药物治疗学分组Vaccines
兽用药物治疗学分组
审评意见日期2026/02/26
欧盟委员会决定日期2026/04/20
修订号
治疗适应症mCombriax is indicated for active immunisation for the prevention of influenza disease and COVID-19 caused by SARS-CoV-2 in individuals 50 years of age and older. The use of this vaccine should be in accordance with official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2026/02/27
最后更新日期2026/04/30
产品说明书
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/mcombriax
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