This double-blind, placebo-controlled study was designed to assess the safety, tolerability, and pharmacokinetics of oral MK-8527 taken once monthly (QM) in participants at low risk for human immunodeficiency virus Type 1 (HIV-1) infection.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Participants With ≥1 Adverse Event (AE)
Timeframe: Up to ~28 weeks
Number of Participants Discontinuing Study Therapy Due to Adverse Event (AE)
Timeframe: Up to ~20 weeks