Gilead Sciences Plans Four Drug Launches This Year to Diversify Beyond HIV

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Gilead Sciences is preparing four drug launches this year as it works to diversify beyond its core HIV franchise. The company reported first-quarter revenue of $7 billion, up 4% year over year, driven by a 10% increase in HIV product sales to $5 billion, while earnings per share rose 54.8% to $1.61. Key launches include bulevirtide, which received accelerated FDA approval on May 22 as the first treatment for chronic hepatitis delta virus infection in certain adults, and a once-daily single-tablet regimen of bictegravir plus lenacapavir for suppressed HIV, with a PDUFA date of August 27. Gilead also expects a decision by December on anito-cel, a multiple myeloma therapy gained through its acquisition of Arcellx, and is expanding use of its breast cancer drug Trodelvy into first-line metastatic triple-negative breast cancer following a June 24 FDA approval. The company’s twice-yearly injectable HIV prevention drug Yeztugo is entering a multimarket launch and is projected to generate $1 billion in 2026 sales. Gilead trades at about 15 times forward earnings and offers a 2.39% dividend yield, having raised its dividend for 11 consecutive years.

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Gilead plans four drug launches this year, including bulevirtide for hepatitis delta and anito-cel for multiple myeloma, expanding beyond HIV.

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