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Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide in a Rapid-Initiation Model of Care for Human Immunodeficiency Virus Type 1 Infection: Primary Analysis of the DIAMOND Study
Author(s) -
Gregory Huhn,
Gordon Crofoot,
Moti Ramgopal,
Joseph Gathe,
Robert Bolan,
Donghan Luo,
Richard Bruce Simonson,
Richard E. Nettles,
Carmela Benson,
Keith Dunn
Publication year - 2019
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/ciz1213
Subject(s) - tenofovir alafenamide , emtricitabine , medicine , darunavir , cobicistat , adverse effect , regimen , clinical endpoint , viral load , human immunodeficiency virus (hiv) , virology , clinical trial , antiretroviral therapy
Most guidelines recommend rapid treatment initiation for patients with newly diagnosed human immunodeficiency virus type 1 (HIV-1) infection, but prospective US data are limited. The DIAMOND (NCT03227861) study using darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) 800/150/200/10 mg is a phase 3 prospective study evaluating efficacy/safety of a single-tablet regimen in a rapid-initiation model of care.

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