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Merck to Present New Data from Clinical Trials Evaluating ISENTRESS® HD (raltegravir) and Investigational HIV Therapies Doravirine and MK-8591 at IAS 2017
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Merck (MRK) Says Three Multiple Myeloma Studies Evaluating KEYTRUDA Placed on Hold After More Deaths
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Merck Provides Further Update on Three Multiple Myeloma Studies Evaluating KEYTRUDA® (pembrolizumab) in Combination with Pomalidomide or Lenalidomide
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UPDATE: Merck (MRK) Confirms Computer Network Compromised
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Merck (MRK) REVEAL Study of Anacetrapib Met Primary Endpoint of Reducing Major Coronary Events
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Merck Provides Update on REVEAL Outcomes Study of Anacetrapib
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Merck (MRK), Premier (PINC) Expand Pact to Address Chronic Care and Vaccination Rates
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Merck and Premier Inc. Expand Collaboration to Address Chronic Care and Vaccination Rates
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Merck (MRK) Presents Update on Multiple Myeloma Studies KEYNOTE-183 & 185 of KEYTRUDA (pembrolizumab) in Combination with Other Therapies
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Merck Provides Update on Multiple Myeloma Studies KEYNOTE-183 and 185 of KEYTRUDA® (pembrolizumab) in Combination with Other Therapies
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Merck and Pfizer Announce that Investigational SGLT-2 Inhibitor Ertugliflozin Met Primary Endpoint in Two Phase 3 Studies
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Merck (MRK) Says Updated Data from KEYNOTE-024 Show Continued Overall Survival Benefit of KEYTRUDA Compared to Chemotherapy in Treatment of Patients with NSCLC with High Levels of PD-L1
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Updated Data from KEYNOTE-024 Show Continued Overall Survival Benefit of Merck’s KEYTRUDA® (pembrolizumab) Compared to Chemotherapy in the First-Line Treatment of Patients with Metastatic Non-Small
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Merck (MRK) Presents New Data From Phase 2 I-SPY 2 TRIAL Shows Improved Outcomes with Combination of KEYTRUDA (pembrolizumab) Plus Standard Neoadjuvant Therapy
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Incyte (INCY), Merck (MRK) Provide Updated Data from ECHO-202 Trial of Epacadostat in Combination with KEYTRUDA
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New Data From Phase 2 I-SPY 2 TRIAL Shows Improved Outcomes with Combination of Merck’s KEYTRUDA® (pembrolizumab) Plus Standard Neoadjuvant Therapy in Patients with High-Risk Breast Cancer
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Updated Data from ECHO-202 Trial of Incyte’s Epacadostat in Combination with Merck’s KEYTRUDA® (Pembrolizumab) Demonstrate Clinical Activity across Multiple Tumor Types
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Merck (MRK) Reports 1+ Year Follow-Up on KEYTRUDA (pembrolizumab) Shows Continued Overall Survival Benefit Over Chemotherapy
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Merck (MRK) Announces New Monotherapy Data for KEYTRUDA (pembrolizumab) in Heavily Pre-Treated Patients with Advanced Gastric Cancer
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Merck (MRK) Reports New Data on Response for Merck’s KEYTRUDA (pembrolizumab) in Advanced Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Solid Tumors
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Merck (MRK) Announces Follow-Up Data with Merck’s KEYTRUDA (pembrolizumab) in Combination with Pemetrexed & Carboplatin at ASCO Meetings
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New Monotherapy Data for Merck’s KEYTRUDA® (pembrolizumab) in Heavily Pre-Treated Patients with Advanced Gastric Cancer to be Presented at 2017 ASCO Annual Meeting
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With More than One-Year Follow-Up, Merck’s KEYTRUDA® (pembrolizumab) Shows Continued Overall Survival Benefit Over Chemotherapy as Second-Line Treatment for Advanced Urothelial Carcinoma Patients P
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Combination of Incyte’s Epacadostat plus Merck’s KEYTRUDA® (pembrolizumab) Demonstrates Activity in Clinical Trial of Patients with Advanced Non-Small Cell Lung Cancer (NSCLC)
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New Data Show Durability of Response for Merck’s KEYTRUDA® (pembrolizumab) in Advanced Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Solid Tumors, Regardless of Tumor
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Longer Term Follow-Up Data with Merck’s KEYTRUDA® (pembrolizumab) in Combination with Pemetrexed and Carboplatin in First-Line Nonsquamous Metastatic Non-Small Cell Lung Cancer (NSCLC) to Be Presen
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Merck (MRK) Announces Updated Longer-Term Overall Survival Data from KEYNOTE-006 Phase 3 Study of KEYTRUDA at ASCO
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With Nearly Three Years of Follow-Up, KEYTRUDA® (pembrolizumab) Data Demonstrated Improved Survival Benefit Compared to Ipilimumab in Advanced Melanoma
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Merck to Present at the Bernstein’s 33rd Annual Strategic Decisions Conference
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Merck Highlights Ongoing Commitment to Fighting Infectious Diseases With More than 20 Data Presentations at ASM Microbe 2017
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Merck (MRK) Announces FDA Approval of ISENTRESS HD Combo for Treatment of HIV-1 Infection
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Merck Receives FDA Approval of ISENTRESS® HD (raltegravir), a New Once-Daily Option, in Combination with Other Antiretroviral Agents, for the Treatment of HIV-1 Infection in Appropriate Patients
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Merck (MRK) Enters License Agreement with Teijin Pharma
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Merck Enters Exclusive Worldwide License Agreement with Teijin Pharma for Investigational Antibody Candidate Targeting Tau
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Merck (MRK) Granted FDA Approval of KEYTRUDA (pembrolizumab) for Adult & Pediatric Patients with Unresectable or Metastatic, Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Adult and Pediatric Patients with Unresectable or Metastatic, Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient Cancer
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Merck Announces Third-Quarter 2017 Dividend
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Merck's (MRK) sBLA for KEYTRUDA to Treat Recurrent or Advanced Gastric or Gastroesophageal Junction Adenocarcinoma Granted FDA Priority Review
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FDA Grants Priority Review to Merck’s Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) for Treatment of Recurrent or Advanced Gastric or Gastroesophageal Junction Ade
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Merck (MRK) Announces Presentation of Phase 2 Results for MK-7264
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Merck Announces Presentation of Phase 2 Results for MK-7264, an Investigational, P2X3 Receptor Antagonist, Being Evaluated for the Treatment of Chronic Cough
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Merck (MRK) Announces CHMP Opinion Recommending Approval of ISENTRESS 600 mg
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Merck Receives CHMP Positive Opinion Recommending Approval of ISENTRESS® (raltegravir) 600 mg in the European Union
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100 Healthy Years - Are Kids Prepared?
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Merck (MRK) Says FDA Approves KEYTRUDA for Two New Indications fo Types of Bladder Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Certain Patients with Locally Advanced or Metastatic Urothelial Carcinoma, a Type of Bladder Cancer
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Merck (MRK) Says Data for KEYTRUDA Across 16 Types of Cancer to Be Presented at ASCO
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Data for KEYTRUDA® (pembrolizumab) Across 16 Types of Cancer from Merck’s Industry-Leading Immuno-Oncology Program to Be Presented at the 2017 ASCO Annual Meeting
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Merck KGaA, Darmstadt, Germany, and Pfizer to Present Data Highlighting Potential of Avelumab in Challenging Cancers at ASCO 2017
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Merck (MRK) to Report New Phase 3 Data on Investigational Ertugliflozin, Additional Analyses of Studies of JANUVIA® (sitagliptin) & Real-World Evidence Research at ADA Meetings

