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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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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260624345655/en/European-Commission-Approves-KEYTRUDA%C2%AE-pembrolizumab-Plus-Padcev%C2%AE-enfortumab-vedotin-ejfv-as-First-PD-1-Inhibitor-Plus-Antibody-Drug-Conjugate-Regimen-for-Adults-With-Cisplatin-Ineligible-Resectable-Muscle-Invasive-Bladder-Cancer/">European Commission Approves KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) as First PD-1 Inhibitor Plus Antibody-Drug Conjugate Regimen for Adults With Cisplatin-Ineligible Resectable Muscle-Invasive Bladder Cancer</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 that KEYTRUDA® (pembrolizumab), Merck&#39;s anti-PD-1 therapy, in combination with Padcev® (enfortumab vedotin-ejfv), an antibody-drug conjugate (ADC), is approved in the European Union (EU), as neoadjuvant treatment and then continued after radical cystectomy (RC) as adjuvant tre...
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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/20260623129832/en/Merck-and-Mae-Partner-to-Expand-Doula-Workforce-and-Address-Maternal-Health-Disparities-in-High-Risk-U.S.-Markets/">Merck and Mae Partner to Expand Doula Workforce and Address Maternal Health Disparities in High-Risk U.S. Markets</a>
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        NEW YORK--(BUSINESS WIRE)--Merck, through the company&#39;s Merck for Mothers initiative, and Mae are collaborating on a multi-state effort to expand and sustain the community-based doula workforce, with a goal of advancing maternal health equity and access for those experiencing the most disparate outcomes. The collaboration will advance doula training, professional development, and ongoing admini...
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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.reuters.com/business/healthcare-pharmaceuticals/mercks-bowel-disease-drug-meets-main-goal-late-stage-trial-2026-06-22/">Merck&#39;s bowel disease drug meets main goal in late-stage trial</a>
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        Merck ​said on ‌Monday its ​drug ​met the ⁠main ​goal in ​a late-stage trial ​testing ​it in ‌patients ⁠with a type ​of ​inflammatory ⁠bowel disease.
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260622057174/en/Merck%E2%80%99s-Tulisokibart-Met-Primary-and-Key-Secondary-Endpoints-in-the-Phase-3-ATLAS-UC-Induction-only-Study-in-Patients-With-Moderately-to-Severely-Active-Ulcerative-Colitis-UC/">Merck&#39;s Tulisokibart Met Primary and Key Secondary Endpoints in the Phase 3 ATLAS-UC Induction-only Study in Patients With Moderately to Severely Active Ulcerative Colitis (UC)</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 positive topline results from the Phase 3 ATLAS-UC induction-only study (Study 2) evaluating tulisokibart (MK-7240), an investigational humanized monoclonal antibody targeting tumor necrosis factor-like cytokine 1A (TL1A), in patients with moderately to severely ...
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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.reuters.com/business/healthcare-pharmaceuticals/mercks-pneumococcal-vaccine-wins-us-approval-high-risk-children-teens-2026-06-18/">Merck&#39;s pneumococcal vaccine wins US approval for high-risk children, teens</a>
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        Drugmaker Merck said on Thursday the U.S. health regulator has approved an expanded use of its ​pneumococcal vaccine for children and teenagers who ‌face a higher risk of catching the bacterial disease due to chronic health conditions.
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260618416609/en/U.S.-FDA-Approves-an-Additional-Indication-for-CAPVAXIVE%C2%AE-Pneumococcal-21-valent-Conjugate-Vaccine-in-Children-and-Adolescents-Aged-2-through-17-at-Increased-Risk-for-Pneumococcal-Disease/">U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) in Children and Adolescents Aged 2 through 17 at Increased Risk for Pneumococcal Disease</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--U.S. FDA Approves an Additional Indication for CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine).
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260617911309/en/Study-Reveals-Dog-Owners-and-Veterinarians-See-Challenges-in-Treating-Allergic-Skin-Disease-Highlighting-a-Need-for-a-Targeted-Rapid-Onset-Treatment-for-Dogs-of-All-Ages/">Study Reveals Dog Owners and Veterinarians See Challenges in Treating Allergic Skin Disease, Highlighting a Need for a Targeted Rapid Onset Treatment for Dogs of All Ages</a>
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        RAHWAY, N.J.--(BUSINESS WIRE)--Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck &amp; Co., Inc., Rahway, N.J., USA (NYSE:MRK), today announced results from a new global survey of dog owners and veterinarians revealing challenges and pain points associated with diagnosing the underlying cause of allergic skin disease in dogs and its treatme...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260616568223/en/Protillion-Biosciences-Announces-Drug-Discovery-Collaboration-with-Merck/">Protillion Biosciences Announces Drug Discovery Collaboration with Merck</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Protillion Biosciences, Inc., a leader in lab-in-the-loop AI drug design, today announced the signing of a multi-target discovery collaboration and license agreement with Merck, known as MSD outside the United States and Canada. The agreement combines Protillion&#39;s proprietary platform with Merck&#39;s global expertise in the discovery of novel therapeutic candidat...
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