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Once-Weekly Oral Islatravir Plus Lenacapavir Maintains High Rates of Virologic Suppression in Adults with HIV

A phase 2 randomized study evaluating the efficacy and safety of once-weekly oral islatravir plus lenacapavir (ISL+LEN) in virologically suppressed adults with HIV found that ISL+LEN maintained high rates of virologic suppression through 48 weeks, with no treatment-related grade 3 or greater adverse events or serious adverse events.

December 22, 2025


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