欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Gardasil
适用类别Human
治疗领域Papillomavirus Infections;Uterine Cervical Dysplasia;Condylomata Acuminata;Immunization
通用名/非专利名称human papillomavirus vaccine [types 6, 11, 16, 18] (recombinant, adsorbed)
活性成分human papillomavirus type 6 L1 protein;human papillomavirus type 11 L1 protein;human papillomavirus type 16 L1 protein;human papillomavirus type 18 L1 protein
产品号EMEA/H/C/000703
患者安全信息No
许可状态Authorised
ATC编码J07BM01
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2006/09/20
上市许可开发者/申请人/持有人Merck Sharp & Dohme B.V. 
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2006/07/27
欧盟委员会决定日期2025/10/20
修订号52
治疗适应症Gardasil is a vaccine for use from the age of 9 years for the prevention of: premalignant genital lesions (cervical, vulvar and vaginal), premalignant anal lesions, cervical cancers and anal cancers causally related to certain oncogenic Human Papillomavirus (HPV) types; genital warts (condyloma acuminata) causally related to specific HPV types. See sections 4.4 and 5.1 for important information on the data that support this indication. The use of Gardasil 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2025/10/20
产品说明书https://www.ema.europa.eu/en/documents/product-information/gardasil-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/gardasil
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase