The purpose of this study is to evaluate the antiviral effect, safety, tolerability, and pharmacokinetics of STP0404 in adult participants living with Human Immunodeficiency Virus Type 1 (HIV-1) infection.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
HIV-1 RNA copies change in plasma
Timeframe: Day 1, Day 11
Total Number of Adverse Events (AEs) occurring through Day 11
Timeframe: Through day 11
Total Number of Serious Adverse Events (SAEs) occurring through Day 11
Timeframe: Through day 11
Mean area under the concentration-time curve from zero to 24 hours (AUC0-24h)
Timeframe: Day 1, Day 10
Mean observed maximum concentration after administration (Cmax)
Timeframe: Day 1, Day 10
Mean time to reach Cmax (Tmax)
Timeframe: Day 1, Day 10
Mean observed concentration at 24 hours after administration (C24h)
Timeframe: Day 2, Day 4, Day 7, Day10, Day 11
Mean area under the concentration-time curve to infinite time (AUCinf)
Timeframe: Day 10
Mean area under the concentration-time curve to time t (AUCt)
Timeframe: Day 10
Mean terminal half-life (t1/2)
Timeframe: Day 10
Mean apparent oral clearance (CL/F)
Timeframe: Day 10
Mean apparent volume of distribution (Vd/F)
Timeframe: Day 10