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US FDA approves Gilead's twice-yearly injection for HIV prevention

  • The U.S. FDA approved Yeztugo, a twice-yearly injectable drug by Gilead Sciences for HIV prevention, on Thursday, June 19, 2025.
  • This approval is based on two clinical trials demonstrating that biannual injections provide almost total prevention of HIV infection, showing greater effectiveness compared to daily preventive pills.
  • Gilead developed lenacapavir, the drug's generic name, after two decades of research overcoming initial challenges with drug stability and efficacy.
  • Greg Millett, who leads public policy efforts at The Foundation for AIDS Research , expressed optimism that this approach could potentially halt HIV transmission, while highlighting that widespread implementation faces significant systemic challenges.
  • Despite the approval's promise, experts warn that healthcare cuts and insurance hurdles may slow adoption and limit reach to populations most at risk.
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Only two injections per year to prevent infection from the HIV virus, instead of the current preventive therapies that, although effective, provide for the administration of one tablet every day. (ANSA)

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Forbes broke the news in United States on Wednesday, June 18, 2025.
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