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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">12 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/us-drugmakers-turn-china-licensing-deals-2026-09-28/">US drugmakers turn to China for licensing deals</a>
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        Merck on Monday agreed to pay Chinese biotech SciBrunch Therapeutics $400 million upfront for global ​rights to an experimental cancer drug, making ‌it the latest US drugmaker to license China-developed medicines.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">12 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/merck-licenses-scibrunch-cancer-drug-deal-worth-up-213-billion-2026-09-28/">Merck licenses SciBrunch cancer drug in deal worth up to $2.13 billion</a>
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        Merck said on Monday it would pay up to $2.13 billion under a ​global licensing deal with China&#39;s SciBrunch Therapeutics ‌for rights to develop, manufacture and sell an experimental cancer treatment.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</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">12 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260928125137/en/Merck-Enters-into-Exclusive-Global-License-Agreement-with-SciBrunch-Therapeutics-for-SPR2015-an-Investigational-Oral-KRAS-G12D-ON-Inhibitor/">Merck Enters into Exclusive Global License Agreement with SciBrunch Therapeutics for SPR2015, an Investigational Oral KRAS G12D (ON) Inhibitor</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, and SciBrunch Therapeutics Co., Ltd. (“SciBrunch”), today announced that they have entered into an exclusive global license agreement for SPR2015, an investigational preclinical oral KRAS G12D (ON) inhibitor.“Evidence continues to accumulate for the therapeutic potential of targeting the KRAS...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">15 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/merck-daiichi-sankyo-withdraw-us-application-lung-cancer-drug-2026-09-25/">Merck, Daiichi Sankyo withdraw US application for lung cancer drug</a>
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        Merck ​and Daiichi ‌Sankyo have ​voluntarily ​withdrawn their ⁠US ​application ​seeking accelerated approval ​for ​their experimental lung ‌cancer ⁠therapy, the ​drugmakers ​said ⁠on Friday.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">15 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260925527975/en/Ifinatamab-Deruxtecan-Biologics-License-Application-for-Certain-Patients-with-Previously-Treated-Extensive-Stage-Small-Cell-Lung-Cancer-Voluntarily-Withdrawn/">Ifinatamab Deruxtecan Biologics License Application for Certain Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn</a>
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        TOKYO--(BUSINESS WIRE)--The Biologics License Application (BLA) seeking accelerated approval in the U.S. for Daiichi Sankyo (TSE: 4568) and Merck&#39;s (NYSE: MRK), known as MSD outside of the United States and Canada, ifinatamab deruxtecan (I-DXd) for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC) with disease progression on or after platinum-based chemothera...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">15 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260925284187/en/Ifinatamab-Deruxtecan-Biologics-License-Application-for-Certain-Patients-with-Previously-Treated-Extensive-Stage-Small-Cell-Lung-Cancer-Voluntarily-Withdrawn/">Ifinatamab Deruxtecan Biologics License Application for Certain Patients with Previously Treated Extensive-Stage Small Cell Lung Cancer Voluntarily Withdrawn</a>
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      <div class="me-0 me-md-5">
        RAHWAY, N.J.--(BUSINESS WIRE)--The Biologics License Application (BLA) seeking accelerated approval in the U.S. for Daiichi Sankyo (TSE: 4568) and Merck&#39;s (NYSE: MRK), known as MSD outside of the United States and Canada, ifinatamab deruxtecan (I-DXd) for the treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC) with disease progression on or after platinum-based che...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">15 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260924674783/en/U.S.-FDA-Approves-WELIREG%C2%AE-belzutifan-Plus-LENVIMA%C2%AE-lenvatinib-for-Certain-Previously-Treated-Adult-Patients-With-Advanced-Renal-Cell-Carcinoma-With-a-Clear-Cell-Component-ccRCC/">U.S. FDA Approves WELIREG® (belzutifan) Plus LENVIMA® (lenvatinib) for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Component (ccRCC)</a>
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        RAHWAY, N.J. &amp; NUTLEY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--FDA Approves WELIREG Plus LENVIMA for Certain Previously Treated Adult Patients With Advanced Renal Cell Carcinoma With a Clear Cell Component (ccRCC).
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Merck-Co-US58933Y1055">Merck &amp; Co.</a></div>
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">16 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/mercks-eye-disease-drug-meets-main-goal-trial-2026-09-24/">Merck&#39;s eye disease drug meets main goal in trial</a>
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        Merck said ​on Thursday ‌its drug met ​the main ​goal in a ⁠mid- ​to late-stage ​trial testing it in ​adult ​patients with a ‌type ⁠of disease that affects blood ​vessels ​at ⁠the back ​of ​the ⁠eye.
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