Gilead's Newly Approved HIV Prevention Drug Poised To Add Billions To Future Sales

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]