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FDA approved Gilead's twice-yearly lenacapavir, marketed as Yeztugo , for HIV pre-exposure prophylaxis on June 18, 2025, based on the PURPOSE 1 and PURPOSE 2 trial program, which Gilead describes as demonstrating superiority "among a broad and geographically diverse range of cisgender men and gender-diverse people" ( [111] )
Expiration Date: 30 JAN 2028
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When not looking at complete adherence to treatment plans, the researchers reported similar results
This differs fundamentally from the chaotic, leaky vessels tumors create to sustain their growth
