欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Bimervax
适用类别Human
治疗领域COVID-19 virus infection
通用名/非专利名称COVID-19 Vaccine (recombinant, adjuvanted)
活性成分SARS-CoV-2 virus recombinant spike (S) protein receptor binding domain (RBD) fusion dimer produced by recombinant DNA technology
产品号EMEA/H/C/006058
患者安全信息No
许可状态Authorised
ATC编码J07BN
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2023/03/30
上市许可开发者/申请人/持有人Hipra Human Health S.L.
人用药物治疗学分组Vaccines
兽用药物治疗学分组
欧盟委员会决定日期2025/10/02
修订号12
治疗适应症Bimervax is indicated as a booster for active immunisation to prevent COVID-19 in individuals 12 years of age and older who have previously received a mRNA COVID-19 vaccine (see sections 4.2 and 5.1). The use of this vaccine should be in accordance with official recommendations. Bimervax XBB.1.16 is indicated for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 12 years of age and older. The use of this vaccine should be in accordance with official recommendations. Bimervax LP.8.1 is indicated for active immunisation to prevent COVID-19 caused by SARS CoV-2 in individuals 12 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2023/03/31
最后更新日期2025/12/09
产品说明书https://www.ema.europa.eu/en/documents/product-information/bimervax-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/bimervax
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