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法规知识库 · EMA 集中审评

Tenofovir disoproxil Zentiva

tenofovir disoproxil phosphate · EMEA/H/C/004120 · 已授权

仿制药

获批上市许可

2016-09-15

欧委会决定日

2025-03-19

持有人 / 申请人

Zentiva k.s.

终止日期字段

无

从产品到官方文件

文件记录

8

官方索引 8

EPAR / 审评

6

assessment / overview 等

产品信息

2

PI / presentations

其他

0

RMP / PIP 等

ATC:J05AF07

治疗领域:HIV Infections

药理分类:Antivirals for systemic use

修订号:16 · 最新影响 PI 的程序:N/0000256696

适应症(原文):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).

关键日期时间轴

来自 EMA medicines JSON 日期字段;缺失字段不展示,不补推结论。

  1. 2025-03-19 · 欧委会决定

  2. 2016-09-15 · 获批上市许可

  3. 2016-07-21 · CHMP 意见通过

说明书、EPAR 与其他文件

仅展示 EMA 官方 document_url;本站不下载或镜像 PDF。

EPAR / 审评资料 6产品信息 2其他 0

EPAR / 审评资料

  • Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation

    procedural-steps-after · 2026-06-11

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  • Tenofovir disoproxil Zentiva : EPAR - Risk management plan

    rmp · 2026-06-11

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  • Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)

    procedural-steps-after · 2024-05-24

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  • Tenofovir disoproxil Zentiva-PSUSA-00002892-201903 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation

    scientific-conclusion · 2020-04-06 · EMA/134602/2020

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  • Tenofovir disoproxil Zentiva : EPAR - Summary for the public

    overview · 2017-03-13

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  • Tenofovir disoproxil Zentiva : EPAR - Public assessment report

    assessment-report · 2017-03-13 · EMA/532453/2016

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产品信息

  • Tenofovir disoproxil Zentiva : EPAR - Product information

    product-information · 2025-03-19

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  • Tenofovir disoproxil Zentiva : EPAR - All Authorised presentations

    all-authorised-presentations · 2017-03-13

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数据来自 EMA 官方 JSON;最终以 EMA / 欧委会文件为准。本页不自动给出安全或非安全结论。