drugset / Trial / NCT05130086

A Study of Islatravir (MK-8591) in Trans and Gender Diverse Participants (MK-8591-035)

NCT05130086

Phase 2 Withdrawn Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelPrevention

Summary

The primary objective of this study is to evaluate the safety and tolerability of Islatravir (ISL) in trans and gender diverse (TGD) participants who are receiving gender-affirming hormone therapy (GAHT) and are at low-risk for human immunodeficiency virus 1 (HIV-1) infection.

Timeline

Start
2022-10-17
Primary completion
2024-03-25
Completion
2024-03-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Islatravir Other / unclassified 60 mg Oral