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emtricitabine/rilpivirine/tenofovir disoproxil (as fumarate) (Eviplera®)

 

Following a limited submission

AWMSG advice

Status: Recommended

Emtricitabine/rilpivirine/tenofovir disoproxil (Eviplera®) is recommended as an option for use within NHS Wales for antiretroviral treatment experienced adults infected with human immunodeficiency virus type 1(HIV-1) without known mutations associated with resistance to the nonnucleoside reverse transcriptase inhibitor (NNRTI) class, tenofovir or emtricitabine, and with a viral load ≤ 100,000 HIV-1 RNA copies/ml. As with other antiretroviral medicinal products, genotypic resistance testing and/or historical resistance data should guide the use of Eviplera®.

 Final Recommendation: emtricitabine-rilpivirine-tenofovirdisoproxil (Eviplera) 2374 (PDF, 346Kb)
 Appraisal Report: emtricitabine-rilpivirine-tenofovir (Eviplera) 2374 (PDF, 302Kb)

Medicine details

Medicine name emtricitabine/rilpivirine/tenofovir disoproxil (as fumarate) (Eviplera®)
Formulation 200 mg/25 mg/245 mg film-coated tablet
Reference number 2374
Indication

Antiretroviral treatment-experienced adults infected with human immunodeficiency virus type 1(HIV-1) without known mutations associated with resistance to the nonnucleoside reverse transcriptase inhibitor (NNRTI) class, tenofovir or emtricitabine, and with a viral load ≤ 100,000 HIV-1 RNA copies/ml. As with other antiretroviral medicinal products, genotypic resistance testing and/or historical resistance data should guide the use of Eviplera®.

Company Gilead Sciences Ltd
BNF chapter Infections
Submission type Limited
Status Recommended
Advice number 1514
NMG meeting date 14/05/2014
AWMSG meeting date 11/06/2014
Ratification by Welsh Government 24/07/2014
Date of issue 25/07/2014
Date of last review 29/09/2014
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