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

  • On Wednesday, the FDA approved Gilead Sciences' twice-yearly injectable drug lenacapavir, marketed as Yeztugo, for HIV prevention in the U.S.
  • Lenacapavir was approved following more than six years of development and extensive clinical trials demonstrating almost complete prevention of HIV when administered as biannual injections.
  • The medication is delivered through a pair of abdominal injections that create a slowly releasing reservoir, cutting the required number of yearly medical appointments in half.
  • One study in sub-Saharan Africa found zero HIV infections among lenacapavir recipients versus 2% in controls, and experts call it the closest alternative to a vaccine.
  • Despite Gilead’s goal to provide access to 2 million people globally, high costs, insurer hurdles, political funding cuts, and health disparities may limit lenacapavir’s reach.
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The United States approved a new treatment to prevent HIV consisting of two injections at a. o.

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Yeztugo prevents HIV with 99.9% effectiveness, but experts warn about access barriers for Latinos in the U.S.

Washington, United States.The U.S. approved a new treatment to prevent HIV, called Yeztugo, announced Wednesday the pharmaceutical laboratory Gilead, which develops it.This treatment called Yeztugo consists of two injections annually and could revolutionize the fight against the Human Immunodeficiency Virus and AIDS.Medicines intended to prevent the transmission of HIV have been in existence for more than a decade, but generally require the taki…

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