欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Tenofovir disoproxil Zentiva
适用类别Human
治疗领域HIV Infections
通用名/非专利名称tenofovir disoproxil
活性成分tenofovir disoproxil phosphate
产品号EMEA/H/C/004120
患者安全信息No
许可状态Authorised
ATC编码J05AF07
是否额外监管No
是否仿制药或hybrid药物Yes
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2016/09/15
上市许可开发者/申请人/持有人Zentiva k.s.
人用药物治疗学分组Antivirals for systemic use
兽用药物治疗学分组
审评意见日期2016/07/21
欧盟委员会决定日期2025/03/19
修订号15
治疗适应症HIV?1 infection Tenofovir disoproxil Zentiva is indicated in combination with other antiretroviral medicinal products for the treatment of HIV?1 infected adults. In adults, the demonstration of the benefit of tenofovir disoproxil in HIV?1 infection is based on results of one study in treatment?naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which tenofovir disoproxil was added to stable background therapy (mainly tritherapy) in antiretroviral pre?treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Tenofovir disoproxil Zentiva is also indicated for the treatment of HIV?1 infected adolescents, with NRTI (nucleotide reverse transcriptase inhibitor) resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of Tenofovir disoproxil Zentiva to treat antiretroviral?experienced patients with HIV?1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Tenofovir disoproxil Zentiva is indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1); evidence of lamivudine-resistant hepatitis B virus (see sections 4.8 and 5.1); decompensated liver disease (see sections 4.4, 4.8 and 5.1). Tenofovir disoproxil Zentiva is indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, persistently elevated serum ALT levels and histological evidence of active inflammation and/or fibrosis (see sections 4.4, 4.8 and 5.1).
适用物种
兽用药物ATC编码
首次发布日期2018/01/18
最后更新日期2025/03/19
产品说明书https://www.ema.europa.eu/en/documents/product-information/tenofovir-disoproxil-zentiva-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/tenofovir-disoproxil-zentiva
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