欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Trumenba
适用类别Human
治疗领域Meningitis, Meningococcal
通用名/非专利名称meningococcal group b vaccine (recombinant, adsorbed)
活性成分Neisseria meningitidis serogroup B fHbp (recombinant lipidated fHbp (factor H binding protein)) subfamily A; Neisseria meningitidis serogroup B fHbp (recombinant lipidated fHbp (factor H binding protein)) subfamily B
产品号EMEA/H/C/004051
患者安全信息No
许可状态Authorised
ATC编码J07AH09
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2017/05/24
上市许可开发者/申请人/持有人Pfizer Europe MA EEIG
人用药物治疗学分组Bacterial vaccines;Meningococcal vaccines
兽用药物治疗学分组
审评意见日期2017/02/23
欧盟委员会决定日期2025/12/17
修订号22
治疗适应症Trumenba is indicated for active immunisation of individuals 10 years and older to prevent invasive meningococcal disease caused by Neisseria meningitidis serogroup B. 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2018/04/11
最后更新日期2025/12/17
产品说明书https://www.ema.europa.eu/en/documents/product-information/trumenba-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/trumenba
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase