欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Heplisav B
适用类别Human
治疗领域Hepatitis B
通用名/非专利名称hepatitis B surface antigen
活性成分hepatitis B surface antigen
产品号EMEA/H/C/005063
患者安全信息No
许可状态Authorised
ATC编码J07BC01
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2021/02/18
上市许可开发者/申请人/持有人Dynavax GmbH
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2020/12/10
欧盟委员会决定日期2024/02/27
修订号7
治疗适应症Heplisav B is indicated for the active immunisation against hepatitis B virus infection (HBV) caused by all known subtypes of hepatitis B virus in adults 18 years of age and older. The use of Heplisav B should be in accordance with official recommendations. It can be expected that hepatitis D will also be prevented by immunisation with Heplisav B as hepatitis D (caused by the delta agent) does not occur in the absence of hepatitis B infection.
适用物种
兽用药物ATC编码
首次发布日期2021/03/01
最后更新日期2025/03/31
产品说明书https://www.ema.europa.eu/en/documents/product-information/heplisav-b-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/heplisav-b
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