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          Positive
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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>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/gilead-paho-agree-hiv-prevention-drug-access-latin-america-caribbean-2026-09-15/">Gilead, PAHO agree on HIV prevention drug access in Latin America, Caribbean</a>
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        U.S. drugmaker Gilead Sciences said on Tuesday it had reached an agreement with the Pan American Health Organization to ​widen access to its HIV prevention drug across Latin ‌America and the Caribbean, as the regions seek to curb new infections.
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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">Business Wire</div>
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        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260915880261/en/Gilead-and-PAHO-Announce-Milestone-Partnership-to-Accelerate-Access-to-Twice-Yearly-Lenacapavir-for-HIV-Prevention-Across-Latin-America-and-the-Caribbean/">Gilead and PAHO Announce Milestone Partnership to Accelerate Access to Twice-Yearly Lenacapavir for HIV Prevention Across Latin America and the Caribbean</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced a new agreement with the Pan American Health Organization (PAHO) to accelerate access to twice-yearly lenacapavir for HIV prevention as pre-exposure prophylaxis (PrEP) across all PAHO Member States in Latin America and the Caribbean. Through PAHO&#39;s Regional Revolving Funds, the agreement establishes a coo...
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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">Business Wire</div>
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        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260908951870/en/Gilead-Opens-State-of-the-Art-Research-Center-to-Advance-the-Next-Generation-of-Medicines/">Gilead Opens State-of-the-Art Research Center to Advance the Next Generation of Medicines</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Opens State-of-the-Art Research Center to Advance the Next Generation of Medicines.
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          Positive
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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>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/us-fda-approves-gileads-once-daily-combination-pill-hiv-treatment-2026-08-27/">US FDA approves Gilead&#39;s once-daily combination pill for HIV treatment</a>
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        The U.S. ​Food and ‌Drug Administration has ​approved ​Gilead Sciences&#39; once ⁠daily ​oral combination ​pill for treatment of ​adults ​whose HIV has ‌already ⁠been reduced to very ​low ​levels, ⁠the company ​said on ​Thursday.
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          Positive
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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>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">CNBC</div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.cnbc.com/2026/08/27/fda-approves-gilead-hiv-pill-bixlenvo-designed-to-simplify-treatment.html">FDA approves daily HIV pill from Gilead designed to simplify treatment for some patients</a>
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        The Food and Drug Administration approved a once-daily HIV pill from Gilead that could help simplify care for some patients whose virus is already under control but who remain on complicated treatment regimens. The tablet combines bictegravir, the backbone of Gilead&#39;s blockbuster HIV pill Biktarvy, with lenacapavir, a centerpiece of the company&#39;s long-term strategy for HIV treatment and prevent...
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          Neutral
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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>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Business Wire</div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260817093045/en/U.S.-FDA-Approves-Gilead%E2%80%99s-Bixlenvo%E2%84%A2-a-New-Once-Daily-Single-Tablet-Option-for-Virologically-Suppressed-Adults-With-HIV-Including-Those-on-Complex-Regimens/">U.S. FDA Approves Gilead&#39;s Bixlenvo™, a New Once-Daily Single Tablet Option for Virologically Suppressed Adults With HIV, Including Those on Complex Regimens</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) approved Bixlenvo™ (bictegravir 75 mg/lenacapavir 50 mg), the smallest once-daily single tablet regimen (STR) for the treatment of HIV in adults who are virologically suppressed. Bixlenvo is now the first and only STR option for virologically suppressed peo...
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          Neutral
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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>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Business Wire</div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260819110838/en/European-Commission-Expands-Role-of-Gilead%E2%80%99s-Trodelvy%C2%AE-in-First-Line-Metastatic-Triple-Negative-Breast-Cancer-Across-PD-L1-Status/">European Commission Expands Role of Gilead&#39;s Trodelvy® in First-Line Metastatic Triple-Negative Breast Cancer Across PD-L1 Status</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced that the European Commission (EC) has granted marketing authorization for Trodelvy® (sacituzumab govitecan-hziy) in combination with Keytruda® (pembrolizumab) for the treatment of adult patients with unresectable, locally advanced or metastatic triple-negative breast cancer (TNBC) who have not received pr...
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          Negative
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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>
        <div class="me-2 text-gray text-size-10">●</div>
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        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.cnbc.com/2026/08/14/court-ruling-gilead-medications-overseas-afps.html">Court rules companies can&#39;t import Gilead medications from overseas in blow to AFP health programs</a>
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        A U.S. Court of Appeals on Thursday upheld a preliminary injunction against several AFPs and related businesses. The ruling could pave the way for the growing alternative funding programs industry to shrink.
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