欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Cervarix
适用类别Human
治疗领域Papillomavirus Infections;Uterine Cervical Dysplasia;Immunization
通用名/非专利名称human papillomavirus vaccine [types 16, 18] (recombinant, adjuvanted, adsorbed)
活性成分human papillomavirus1 type 16 L1 protein;human papillomavirus type 18 L1 protein
产品号EMEA/H/C/000721
患者安全信息No
许可状态Authorised
ATC编码J07BM02
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2007/09/20
上市许可开发者/申请人/持有人GlaxoSmithKline Biologicals S.A.
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2023/04/26
修订号42
治疗适应症Cervarix is a vaccine for use from the age of 9 years for the prevention of premalignant ano-genital lesions (cervical, vulvar, vaginal and anal) and cervical and anal cancers causally related to certain oncogenic Human Papillomavirus (HPV) types. See sections 4.4 and 5.1 for important information on the data that support this indication. The use of Cervarix should be in accordance with official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2018/05/17
最后更新日期2024/11/26
产品说明书https://www.ema.europa.eu/en/documents/product-information/cervarix-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/cervarix
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