Stopped: Voluntarily terminated due to benefit/risk assessment.
The main purpose of the study is to evaluate the safety and tolerability of oral Islatravir (ISL) once monthly (QM) as Preexposure Prophylaxis (PrEP) in cisgender men who have sex with men (MSM) and transgender women (TGW) who have sex with men and who are at high risk of HIV-1 infection with 48 or 96 weeks of treatment and a minimum follow-up of 42 days.
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Number of Participants Who Experienced an Adverse Event (AE) During Blinded Treatment
Timeframe: Up to approximately 10.5 months
Number of Participants Who Discontinued From Blinded Study Treatment Due to an AE
Timeframe: Up to approximately 9 months