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法规知识库 · EMA 集中审评

Efavirenz/Emtricitabine/Tenofovir disoproxil Krka

efavirenz;emtricitabine;tenofovir disoproxil succinate · EMEA/H/C/004274 · 已授权

仿制药

获批上市许可

2018-02-08

欧委会决定日

2025-01-16

持有人 / 申请人

KRKA tovarna zdravil d.d. Novo mesto

终止日期字段

无

从产品到官方文件

文件记录

7

官方索引 7

EPAR / 审评

5

assessment / overview 等

产品信息

2

PI / presentations

其他

0

RMP / PIP 等

ATC:J05AR06

治疗领域:HIV Infections

药理分类:Antivirals for systemic use

修订号:13 · 最新影响 PI 的程序:N/0000241468

适应症(原文):Efavirenz/Emtricitabine/Tenofovir disoproxil Krka is a fixed-dose combination of efavirenz, emtricitabine and tenofovir disoproxil. It is indicated for the treatment of human immunodeficiency virus-1 (HIV-1) infection in adults aged 18 years and over with virologic suppression to HIV-1 RNA levels of < 50 copies/ml on their current combination antiretroviral therapy for more than three months. Patients must not have experienced virological failure on any prior antiretroviral therapy and must be known not to have harboured virus strains with mutations conferring significant resistance to any of the three components contained in Efavirenz/Emtricitabine/Tenofovir disoproxil Krka prior to initiation of their first antiretroviral treatment regimen. The demonstration of the benefit of efavirenz/emtricitabine/tenofovir disoproxil is primarily based on 48-week data from a clinical study in which patients with stable virologic suppression on a combination antiretroviral therapy changed to efavirenz/emtricitabine/tenofovir disoproxil. No data are currently available from clinical studies with efavirenz/emtricitabine/tenofovir disoproxil in treatment-naïve or in heavily pretreated patients. No data are available to support the combination of efavirenz/emtricitabine/tenofovir disoproxil and other antiretroviral agents.

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. 2025-01-16 · 欧委会决定

  2. 2018-02-08 · 获批上市许可

  3. 2017-12-14 · 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 5产品信息 2其他 0

EPAR / 审评资料

  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Procedural steps taken and scientific information after authorisation

    procedural-steps-after · 2025-01-22

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  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)

    procedural-steps-after · 2024-07-19

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  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Risk-management-plan summary

    rmp-summary · 2020-03-17

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  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Summary for the public

    overview · 2018-02-20 · EMA/9058/2018

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  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Public assessment report

    assessment-report · 2018-02-20 · EMA/846772/2017

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产品信息

  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Product information

    product-information · 2025-01-22

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  • Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - All Authorised presentations

    all-authorised-presentations · 2018-02-20

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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。