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FDA Approves Lenacapavir (Yeztugo) as Twice-Yearly HIV Prevention Injection

FDA Approves Lenacapavir (Yeztugo) as Twice-Yearly HIV Prevention Injection

FDA Approves Lenacapavir (Yeztugo) as Twice-Yearly HIV Prevention Injection On June 19, 2025, the Food and Drug Administration (FDA) approved lenacapavir, marketed as Yeztugo, as the first twice-yearly injection for pre-exposure prophylaxis (PrEP) to prevent HIV infection. Previously approved in 2012 under the name Sunlenca as a treatment for HIV in individuals who no longer responded to other medications, lenacapavir’s mechanism involves targeting a protective shell HIV needs to survive, disrupting its growth and spread. Unlike most HIV drugs that…

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Lenacapavir: A Twice-Yearly HIV Prevention Injection Approved by the FDA – Promise and Challenges

Lenacapavir: A Twice-Yearly HIV Prevention Injection Approved by the FDA – Promise and Challenges

Lenacapavir: A Twice-Yearly HIV Prevention Injection Approved by the FDA – Promise and Challenges The Food and Drug Administration (FDA) has approved Gilead Sciences’ lenacapavir as a twice-yearly pre-exposure prophylaxis (PrEP) injection, marking a significant advancement in HIV prevention. This approval follows successful Phase III clinical trials demonstrating a remarkably high efficacy rate, exceeding that of daily PrEP regimens. The drug, marketed under the brand name Yeztugo, achieved a 100% prevention rate in cisgender women and a 99.9% prevention rate…

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