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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Gilead-Sciences-US3755581036">Gilead Sciences</a></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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      <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="text-gray">vor etwa einem Monat</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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      <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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      <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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      <a target="_blank" rel="nofollow" href="https://seekingalpha.com/article/4907521-why-gilead-sciences-is-now-a-hold-rating-upgrade">Why Gilead Sciences Is Now A Hold (Rating Upgrade)</a>
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        Gilead Sciences, Inc. once again demonstrated strong performance of Trodelvy, Livdelzi, and Yeztugo. This &quot;trio&quot; generated $701 million in revenue for Gilead in Q1, up 110.5% quarter-on-quarter. However, Gilead&#39;s cell therapy franchise is once again struggling, with sales of Yescarta and Tecartus falling 12.3% YoY.
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260520959712/en/Gilead-Sciences-Completes-Acquisition-of-Tubulis-Further-Strengthening-Oncology-Portfolio/">Gilead Sciences Completes Acquisition of Tubulis Further Strengthening Oncology Portfolio</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced the successful completion of its previously announced acquisition of Tubulis GmbH, a private Germany-based, clinical-stage biotechnology company developing next-generation antibody-drug conjugates (ADCs). The acquisition brings Gilead next-generation ADC assets and a platform designed to maximize patient ...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260521945977/en/Gilead-Sciences-and-World-Health-Organization-Expand-Collaboration-to-Help-Eliminate-Visceral-Leishmaniasis-a-Fatal-Parasitic-Disease/">Gilead Sciences and World Health Organization Expand Collaboration to Help Eliminate Visceral Leishmaniasis, a Fatal Parasitic Disease</a>
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        FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences, Inc. (Nasdaq: GILD) today announced a renewed five-year collaboration with the World Health Organization (WHO), committing funding, strategic support and product donations to accelerate progress toward eliminating visceral leishmaniasis (VL), also known as kala-azar. VL, the second deadliest parasitic disease after malaria, is a sandfly-bor...
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