Core Insights - The FDA approved Gilead Sciences' Yeztugo (lenacapavir) as the first and only twice-yearly PrEP option in the U.S. for HIV prevention, showing ≥99.9% efficacy in trials [1][2][5] - The European Medicines Agency's CHMP has recommended lenacapavir for PrEP, with a final decision from the European Commission expected later this year [2][3] - Positive trial results indicate lenacapavir's superiority over daily oral Truvada in preventing HIV infections [4][5] Company Developments - Gilead's Yeztugo could significantly contribute to revenue, with projections of $4.1 billion in sales by 2030 and $6.4 billion by 2035, driven by its ease of use compared to current treatments [6][7] - Needham upgraded Gilead's stock rating from Hold to Buy, forecasting a price of $133 based on positive physician feedback and market potential [6] Market Outlook - The HIV prevention market is expected to grow by approximately 49% by 2030, with Yeztugo anticipated to capture about 38% of this growth [7] - Gilead's revenue heavily relies on its HIV drugs, with around 70% coming from this segment, making Yeztugo a crucial growth driver [7]

Core Viewpoint - Gilead China has officially launched Lenacapavir, a groundbreaking HIV pre-exposure prophylaxis (PrEP) drug that requires administration only twice a year, in the Boao Lecheng International Medical Tourism Pilot Zone in Hainan [1] Group 1 - Lenacapavir has been approved for use in the United States since June, aimed at reducing the risk of HIV transmission through sexual contact for adults and adolescents weighing at least 35 kilograms [1]