欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tybost
适用类别Human
治疗领域HIV Infections
通用名/非专利名称cobicistat
活性成分cobicistat
产品号EMEA/H/C/002572
患者安全信息No
许可状态Authorised
ATC编码V03AX03
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2013/09/19
上市许可开发者/申请人/持有人Gilead Sciences Ireland UC
人用药物治疗学分组Antivirals for systemic use
兽用药物治疗学分组
欧盟委员会决定日期2023/02/13
修订号15
治疗适应症Tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (HIV-1) infected adults and adolescents aged 12 years and older: weighing at least 35 kg co?administered with atazanavir or weighing at least 40 kg co?administered with darunavir.
适用物种
兽用药物ATC编码
首次发布日期2018/07/26
最后更新日期2023/02/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/tybost-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tybost
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