HomeTrialNCT05052996
🔬NCT05052996Phase 2ACTIVE NOT RECRUITING

Study Evaluating the Safety and Efficacy of Islatravir in Combination With Lenacapavir in Virologically Suppressed People With HIV

Study Summary

The primary objective of this study is to evaluate the efficacy of oral weekly islatravir (ISL) in combination with lenacapavir (LEN) in virologically suppressed people with HIV (PWH) at Week 24.

Conditions
Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment142 participants
Primary Completion
Lead SponsorGilead Sciences
Data Retrieved2026-04-11 02:55:27.113267+00:00
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