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Merck’s Investigational NNRTI, Doravirine, Meets Primary Efficacy Endpoint of Non-Inferiority to Efavirenz, Both in Combination with Other Antiretroviral Agents, in Pivotal Phase 3 Trial for Treatme
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Merck (MRK) Says Phase 3 Study of KEYTRUDA Monotherapy in Patients with Previously Treated Recurrent or Metastatic HNSCC Didn't Meet Primary Endpoint
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Merck Provides Update on Phase 3 Study of KEYTRUDA® (pembrolizumab) Monotherapy in Patients with Previously Treated Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)
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Merck (MRK) Announces U.S. Launch of RENFLEXIS
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Merck Announces U.S. Launch of RENFLEXIS™ (infliximab-abda), a Biosimilar of Remicade, for All Eligible Indications
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Merck (MRK) Announces Week 96 Results from ONCEMRK Study Evaluating ISENTRESS HD
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Merck Announces Week 96 Results from ONCEMRK, A Study Evaluating Once-Daily ISENTRESS® HD (raltegravir), in Combination with Other Antiretroviral Agents, for the Treatment of HIV-1 Infection in Appro
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EMA's CHMP Issues Positive Opinion for Avelumab for the Treatment of Metastatic Merkel Cell Carcinoma
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Merck (MRK) Announces EMA's CHMP Recommends Approval for KEYTRUDA for Treatment of Certain Patients with Locally Advanced or Metastatic Urothelial Carcinoma
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European Medicines Agency’s CHMP Recommends Approval for Merck’s KEYTRUDA® (pembrolizumab) for the Treatment of Certain Patients with Locally Advanced or Metastatic Urothelial Carcinoma, a Type o
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Merck (MRK) and Pfizer (PFE) Collaborate with Corning (GLW) to Modernize Pharmaceutical Glass Packaging
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Merck and Pfizer Collaborate with Corning to Modernize Pharmaceutical Glass Packaging
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Merck (MRK) Granted Tentative Approval for LUSDUNA Nexvue (insulin glargine injection)
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Merck Announces U.S. FDA Grants Tentative Approval for LUSDUNA™ Nexvue™ (insulin glargine injection), a Follow-On Biologic Basal Insulin
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Merck (MRK) Announces Presentations of Clinical and Real-World Data AAIC
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Merck Announces Presentations of Clinical and Real-World Data at The Alzheimer’s Association International Conference®
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Merck to Hold Second-Quarter 2017 Sales and Earnings Conference Call on July 28
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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

