The proposed study is a phase 1, open label, randomized study to evaluate the safety and antiretroviral activity of seven infusions of 3BNC117 and 10-1074, administered intravenously at 30 mg/kg dose level, in human immunodeficiency virus (HIV)-infected individuals on combination antiretroviral therapy (ART) and during an analytical interruption of ART.
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The change in the size of the functional, latent HIV-1 reservoir between baseline and after seven infusions of 3BNC117 and 10-1074
Timeframe: Day 0 and week 26
The size of the proviral HIV-1 reservoir
Timeframe: 48 weeks
The rate of viral rebound
Timeframe: Week 12 (group 1) and week 38 (group 2)
Time to return of HIV-1 viremia
Timeframe: 48 weeks
The rate of adverse events (AE) and serious adverse events (SAE).
Timeframe: 48 weeks
The severity of adverse events (AE) and serious adverse events (SAE).
Timeframe: 48 weeks