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EMA Product

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva

Product approved by European Medicines Agency (EU)

Basic Information

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva

Regulatory Information

EMEA/H/C/004250

Authorised

July 17, 2017

May 18, 2017

12

March 18, 2025

Company Information

Czech Republic

U kabelovny 130 Dolni Mecholupy 102 37 Prague 10

Zentiva, k.s.

Drug Classification

Generic Medicine

Active Substances Detail

efavirenzemtricitabinetenofovir disoproxil phosphate

Detailed Information

Therapeutic Indication

### Therapeutic indication Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva 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 Zentiva prior to initiation of their first antiretroviral treatment regimen. The demonstration of the benefit of the combination 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 combination 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.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use the medicine. For practical information about using Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva, patients should read the package leaflet or contact their doctor or pharmacist.

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