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A Trial of a Single-tablet Regimen of Elvitegravir, Cobicistat, Emtricitabine, and Tenofovir Disoproxil Fumarate for the Initial Treatment of Human Immunodeficiency Virus Type 2 Infection in a Resource-limited Setting: 48-Week Results From Senegal, West Africa
Author(s) -
Selly Ba,
Da. Raugi,
Robert A. Smith,
Fatima Sall,
Khadim Faye,
Stephen E. Hawes,
Papa Salif Sow,
Moussa Seydi,
Geoffrey S. Gottlieb,
Fatou Traoré,
Marie Pierre Sy,
Bintou Diaw,
Mbaye Ndoye,
Amadou Bale Diop,
Marianne Fadam Diome,
Alassane Niang,
Jean Jacques Malomar,
ElHadji Ibrahima Sall,
Ousseynou Cisse,
Ibrahima Tito Tamba,
Jean Philippe Diatta,
Jacques F. Sambou,
Raphael Bakhoum,
Juliette Gomis,
Noelle A. Benzekri,
John Lin,
Nancy B. Kiviat,
Sally Leong,
Sara Masoum,
Vincent H. Wu,
Carol Gallardo,
Eleanor Espinosa,
Ming Chang,
Bob Coombs
Publication year - 2018
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/ciy324
Subject(s) - medicine , elvitegravir , emtricitabine , cobicistat , regimen , viral load , adverse effect , tolerability , virology , reverse transcriptase inhibitor , human immunodeficiency virus (hiv) , antiretroviral therapy
Our trial of a single-tablet regimen containing elvitegravir, cobicistat, emtricitabine, and tenofovir disoproxil fumarate in antiretroviral therapy–naive HIV-2–infected individuals for 48 weeks, in a resource-limited setting, demonstrated favorable immunovirologic outcomes and was well tolerated.

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