<turbo-stream action="append" target="news"><template>  <div class="row mb-4 py-2 news-box">
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Gilead-Sciences-US3755581036">Gilead Sciences</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260605187130/en/Gilead-Applauds-Collaborative-Efforts-to-Launch-Lenacapavir-for-HIV-Prevention-in-South-Africa/">Gilead Applauds Collaborative Efforts to Launch Lenacapavir for HIV Prevention in South Africa</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)-- #Access--Gilead applauds the leadership of the Government of South Africa and the Global Fund for accelerating access to lenacapavir, a long-acting HIV prevention medication. This marks an important step toward expanding access to lenacapavir for communities most affected by HIV. “South Africa is at the heart of global efforts to end HIV. With the country&#39;...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Gilead-Sciences-US3755581036">Gilead Sciences</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/04/3307098/0/en/GILEAD-SCIENCES-AND-LAKEFRONT-COMPLETE-ACQUISITION-OF-OURO-MEDICINES-TO-FURTHER-EXPAND-INFLAMMATION-PIPELINE.html">GILEAD SCIENCES AND LAKEFRONT COMPLETE ACQUISITION OF OURO MEDICINES TO FURTHER EXPAND INFLAMMATION PIPELINE</a>
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        Companies will collaborate on the development of gamgertamig, a potential first-in-class and best-in-class T cell engager in autoimmune diseases
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Gilead-Sciences-US3755581036">Gilead Sciences</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260602237640/en/Gilead%E2%80%99s-Livdelzi%C2%AE-Seladelpar-Delivers-Statistically-Significant-Composite-ALP-Normalization-in-Phase-3-IDEAL-Trial-in-Primary-Biliary-Cholangitis-PBC/">Gilead&#39;s Livdelzi® (Seladelpar) Delivers Statistically Significant Composite ALP Normalization in Phase 3 IDEAL Trial in Primary Biliary Cholangitis (PBC)</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced positive results from a Phase 3 study in people with primary biliary cholangitis (PBC), showing that treatment with Livdelzi® (seladelpar) led to significantly more patients achieving normalization of alkaline phosphatase (ALP), a key liver marker of disease progression, compared with placebo after 52 wee...
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260526228499/en/Phase-3-ASSURE-Interim-Data-Majority-of-People-in-the-Study-with-ALP-1%E2%80%931.67%C3%97ULN-Achieved-High-and-Sustained-Composite-ALP-Normalization-at-24-Months-with-Gilead%E2%80%99s-Livdelzi-Seladelpar/">Phase 3 ASSURE Interim Data: Majority of People in the Study with ALP 1–1.67×ULN Achieved High and Sustained Composite ALP Normalization at 24 Months with Gilead&#39;s Livdelzi (Seladelpar)</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today shared new results from a post hoc analysis showing that Livdelzi® (seladelpar) was associated with high and sustained rates of normalization of a key liver marker (ALP) in people living with primary biliary cholangitis (PBC). In an ongoing Phase 3 study, participants with elevated ALP levels (between 1.0 and 1.67×...
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-gileads-drug-deadly-liver-infection-2026-05-22/">US FDA approves Gilead&#39;s drug for deadly liver infection</a>
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        The U.S. Food and ​Drug Administration said on ‌Friday it approved Gilead Sciences&#39; drug for a rare and ​deadly liver infection that previously ​had no approved treatment options.
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260522569258/en/FDA-Grants-Accelerated-Approval-to-Gilead%E2%80%99s-Hepcludex%C2%AE-bulevirtide-gmod-the-First-and-Only-Approved-Treatment-for-Chronic-Hepatitis-Delta-Virus-HDV/">FDA Grants Accelerated Approval to Gilead&#39;s Hepcludex® (bulevirtide-gmod), the First and Only Approved Treatment for Chronic Hepatitis Delta Virus (HDV)</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval for Hepcludex® (bulevirtide-gmod) 8.5 mg for the treatment of adults living with chronic hepatitis delta virus (HDV) infection, making it the first and only approved treatment for HDV in the United States. The FDA granted ac...
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260521052840/en/Gilead-Receives-CHMP-Positive-Opinion-for-Trodelvy%C2%AE-in-First-Line-Metastatic-Triple-Negative-Breast-Cancer-for-Patients-Not-Candidates-for-PD--L-1-Inhibitors/">Gilead Receives CHMP Positive Opinion for Trodelvy® in First-Line Metastatic Triple-Negative Breast Cancer for Patients Not Candidates for PD-(L)1 Inhibitors</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion, recommending the marketing authorization of Trodelvy® (sacituzumab govitecan-hziy) as a monotherapy for the treatment of adult patients with unresectable locally advanced o...
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260520344508/en/New-ASCO-and-EHA-2026-Data-Demonstrate-Gilead-and-Kite%E2%80%99s-Momentum-Across-Antibody-Drug-Conjugates-and-Cell-Therapy-in-Oncology/">New ASCO and EHA 2026 Data Demonstrate Gilead and Kite&#39;s Momentum Across Antibody-Drug Conjugates and Cell Therapy in Oncology</a>
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        FOSTER CITY, Calif. &amp; SANTA MONICA, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that together with Kite, a Gilead company, it will present more than 25 abstracts, including six oral presentations, at the 2026 ASCO Annual Meeting (May 29 – June 2) and the 2026 EHA Congress (June 11 – 14). These presentations underscore the increasing diversity of Gilead&#39;s oncolo...
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