The purpose of this study is to assess the percent change in body weight when switching to darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) fixed-dose combination (FDC) (Immediate Switch Arm) compared to continuing the current integrase (INI) + tenofovir alafenamide/emtricitabine (TAF/FTC) antiretroviral (ARV) regimen (Delayed Switch Arm) in virologically-suppressed human immunodeficiency virus (HIV)-1 infected participants who have experienced rapid and significant body weight gain.
|Treatment||D/C/F/TAF FDC, TAF/FTC FDC, INI Based Regimen|
|Clinical Study Identifier||NCT04442737|
|Sponsor||Janssen Scientific Affairs, LLC|
|Last Modified on||31 December 2020|
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