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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-DE0006599905">Merck</a></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.businesswire.com/news/home/20260715942620/en/Merck%E2%80%99s-LIPFENDRA%C2%AE-enlicitide-is-the-First-and-Only-Once-Daily-Oral-PCSK9-Inhibitor-Approved-by-the-U.S.-FDA-to-Reduce-LDL-C-in-Adults-with-Hypercholesterolemia/">Merck&#39;s LIPFENDRA® (enlicitide) is the First and Only Once-Daily Oral PCSK9 Inhibitor Approved by the U.S. FDA to Reduce LDL-C in Adults with Hypercholesterolemia</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)--Merck&#39;s LIPFENDRA is the First and Only Once-Daily Oral PCSK9 Inhibitor Approved by the U.S. FDA to Reduce LDL-C in Adults with Hypercholesterolemia.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-DE0006599905">Merck</a></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.wsj.com/health/pharma/mercks-first-of-its-kind-cholesterol-pill-approved-ushering-in-new-wave-of-treatment-3e30d0e7">The FDA approved Lipfendra, a first-of-its kind pill from Merck that is designed to help lower cholesterol levels beyond what statins alone can achieve</a>
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        Lipfendra, to be taken once a day, is designed to help lower cholesterol levels beyond what statins alone can achieve.
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          Positive
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-DE0006599905">Merck</a></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.investors.com/news/technology/merck-stock-adc-kelun-biotech-lung-cancer/">Dow Jones&#39; Merck Scores A Win With Cancer Smart Bomb</a>
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        Merck stock popped Wednesday on the back of positive test results for a new treatment combo in a common form of lung cancer.
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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.businesswire.com/news/home/20260710192353/en/FDA-Approves-KEYTRUDA%C2%AE-pembrolizumab-and-KEYTRUDA-QLEX%E2%84%A2-pembrolizumab-and-berahyaluronidase-alfa-pmph-Each-With-Padcev%C2%AE-enfortumab-vedotin-ejfv-as-Treatment-Before-and-After-Surgery-for-Adults-With-Muscle-Invasive-Bladder-Cancer-MIBC/">FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Each With Padcev® (enfortumab vedotin-ejfv), as Treatment Before and After Surgery for Adults With Muscle-Invasive Bladder Cancer (MIBC)</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) approved KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), Merck&#39;s anti-PD-1 therapies, each in combination with Padcev® (enfortumab vedotin-ejfv), as neoadjuvant treatment and then continu...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-DE0006599905">Merck</a></div>
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.investors.com/stock-lists/new-highs/merck-stock-mrk-jpmorgan-chase-jpm-amphenol-aph-medicare-alignment-healthcare-alhc/">Merck Stock, JPMorgan And Two Others Hit New Highs</a>
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        Merck stock is in a buy zone after hitting a new high. Fellow Dow stock JPMorgan Chase and Amphenol are both trading around entry points.
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          Negative
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-DE0006599905">Merck</a></div>
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.proactiveinvestors.com/companies/news/1094734?SNAPI">Merck, AbbVie probed by US lawmakers over China clinical trials: report</a>
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        A bipartisan group of United States lawmakers has opened national security investigations into whether five major pharmaceutical companies, including Merck and AbbVie, were involved in clinical trials conducted in China that may have supported the country&#39;s military capabilities, according to a Reuters report. The inquiry, led by Republican Representative John Moolenaar of Michigan, chair of th...
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260629823507/en/Merck-Announces-New-Agreement-with-ADAP-Crisis-Task-Force-to-Improve-Access-and-Care-for-People-Living-with-HIV/">Merck Announces New Agreement with ADAP Crisis Task Force to Improve Access and Care for People Living with HIV</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck Announces Agreement to Improve Treatment Access for People Living with HIV. Agreement will help state ADAP programs provide access to IDVYNSO.
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260625926870/en/FDA-Approves-KEYTRUDA%C2%AE-pembrolizumab-and-KEYTRUDA-QLEX%E2%84%A2-pembrolizumab-and-berahyaluronidase-alfa-pmph-each-with-Trodelvy%C2%AE-sacituzumab-govitecan-hziy-as-First-Line-Treatment-of-PD-L1-CPS-%E2%89%A510-Advanced-Triple-Negative-Breast-Cancer-TNBC/">FDA Approves KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), each with Trodelvy® (sacituzumab govitecan-hziy) as First-Line Treatment of PD-L1+ (CPS ≥10) Advanced Triple-Negative Breast Cancer (TNBC)</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) approved KEYTRUDA® (pembrolizumab) and KEYTRUDA QLEX™ (pembrolizumab and berahyaluronidase alfa-pmph), each in combination with Trodelvy® (sacituzumab govitecan-hziy), Gilead&#39;s Trop-2-directed antibody-drug conjugate (A...
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