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4/25 - 10:57 AM \; \;Dow Movers: IBM, MRK [VIDEO]
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4/19 - 7:06 AM \; \;Health Canada Approves KEYTRUDA®\; as a first-line treatment for adult patients with locally advanced unresectable or metastatic HER2-negative gastric or gastroesophageal junction (GEJ) adenocarcinoma in combination with fluoropyrimidine- and platinum-containing chemotherapy
4/19 - 7:05 AM \; \;Health Canada Approves KEYTRUDA as a first-line treatment for adult patients with locally advanced unresectable or metastatic HER2-negative gastric or gastroesophageal junction (GEJ) adenocarcinoma in combination with fluoropyrimidine- and platinum-containing chemotherapy
4/4 - 6:45 AM \; \;Merck Initiates Phase 3 Clinical Trial of MK-1084, an Investigational Oral KRAS G12C Inhibitor, in Combination with KEYTRUDA (pembrolizumab) for First-Line Treatment of Certain Patients With Metastatic Non-Small Cell Lung Cancer
4/3 - 8:00 AM \; \;REJOICE-Ovarian01 Phase 2/3 Trial of Raludotatug Deruxtecan Initiated in Patients with Platinum-Resistant Ovarian Cancer
4/1 - 6:45 AM \; \;Merck to Hold First-Quarter 2024 Sales and Earnings Conference Call April 25
3/28 - 9:16 AM \; \;How We Can Strengthen Vaccination Programs and Build Vaccine Confidence Together
3/28 - 6:45 AM \; \;European Commission Approves Merck\'s KEYTRUDA (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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3/26 - 6:21 PM \; \;FDA Approves Merck\'s WINREVAIR™\; (sotatercept-csrk), a First-in-Class Treatment for Adults with Pulmonary Arterial Hypertension (PAH, WHO Group 1)
3/26 - 9:31 AM \; \;Merck Foundation Strengthens Its Commitment to Expanding Access to Care in Asia-Pacific Region
3/21 - 6:45 AM \; \;Merck Provides Update on Phase 3 KEYLYNK-006 Trial Evaluating KEYTRUDA (pembrolizumab) Plus Maintenance LYNPARZA (olaparib) for Certain Patients With Metastatic Nonsquamous Non-Small Cell Lung Cancer
3/20 - 10:13 AM \; \;Dow Movers: CAT, CSCO [VIDEO]
3/19 - 9:00 AM \; \;Merck Announces Positive Data on V116, an Investigational, 21-Valent Pneumococcal Conjugate Vaccine Specifically Designed for Adults, Demonstrated Immune Responses in Adults
3/15 - 4:25 PM \; \;FarmSee Ltd Announces the Completion of a Minority Investment in its Swine Monitoring Platform
3/15 - 6:45 AM \; \;Merck\'s KEYTRUDA (pembrolizumab) Plus Chemoradiotherapy (CRT) Significantly Improved Overall Survival (OS) Versus CRT Alone in Patients With Newly Diagnosed High-Risk Locally Advanced Cervical Cancer
3/13 - 3:00 AM \; \;Merck Announces Plans to Conduct Clinical Trials of a Novel Investigational Multi-Valent Human Papillomavirus (HPV) Vaccine and Single-Dose Regimen for GARDASIL9
3/11 - 8:15 AM \; \;Merck Completes Acquisition of Harpoon Therapeutics, Inc.
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