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Merck Animal Health Completes Acquisition of U.S. Rights to SENTINEL® Brand of Combination Parasiticides for Companion Animals
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Merck and Ridgeback Bio Announce Closing of Collaboration and Licensing Transaction
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Merck to Hold Second-Quarter 2020 Sales and Earnings Conference Call on July 31
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FDA Approves BAVENCIO as First-Line Maintenance Treatment for Patients with Locally Advanced or Metastatic Urothelial Carcinoma
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Merck (MRK) Announces FDA Approves its KEYTRUDA for First-Line Treatment of Patients With Unresectable or Metastatic MSI-H or dMMR Colorectal Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for First-Line Treatment of Patients With Unresectable or Metastatic MSI-H or dMMR Colorectal Cancer
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Merck (MRK) Announces FDA Approves KEYTRUDA for Treatment of Patients with Recurrent or Metastatic cSCC that is Not Curable by Surgery or Radiation
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for the Treatment of Patients with Recurrent or Metastatic Cutaneous Squamous Cell Carcinoma (cSCC) that is Not Curable by Surgery or Radiation
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Merck (MRK) Underscores Commitment to HIV with New Data Analyses to be Presented at AIDS 2020: Virtual
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Merck Underscores Commitment to HIV with New Data Analyses to be Presented at AIDS 2020: Virtual
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Merck (MRK) Announces V114, Its Investigational 15-valent Pneumococcal Conjugate Vaccine, Met Safety and Immunogenicity Objectives in Initial Phase 3 Studies in Adults
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Merck Announces That V114, Its Investigational 15-valent Pneumococcal Conjugate Vaccine, Met Safety and Immunogenicity Objectives in Initial Phase 3 Studies in Adults
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Merck (MRK) Announces KEYTRUDA Approved in China for Second-Line Treatment of Patients with Locally Advanced or Metastatic Esophageal Squamous Cell Carcinoma Whose Tumors Express PD-L1 (CPS ≥10)
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Merck’s KEYTRUDA® (pembrolizumab) Approved in China for Second-Line Treatment of Patients with Locally Advanced or Metastatic Esophageal Squamous Cell Carcinoma Whose Tumors Express PD-L1 (CPS ≥1
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Merck Completes Acquisition of Themis
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Merck Animal Health Completes Acquisition of Quantified Ag®
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Merck (MRK) Announces FDA Approves Second Biomarker-Based Indication for KEYTRUDA, Regardless of Tumor Type
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FDA Approves Second Biomarker-Based Indication for Merck’s KEYTRUDA® (pembrolizumab), Regardless of Tumor Type
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Merck (MRK), Pfizer (PFE) Report SGLT2 Inhibitor STEGLATROTM (ertugliflozin) Meets Primary Endpoint in VERTIS CV Trial for Patients with Type 2 Diabetes & Atherosclerotic Cardiovascular Disease
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Merck and Pfizer’s SGLT2 Inhibitor STEGLATROTM (ertugliflozin) Meets Primary Endpoint in VERTIS CV Trial for Patients with Type 2 Diabetes and Atherosclerotic Cardiovascular Disease
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Merck Announces Call for Proposals for Second Cohort of Safer Childbirth Cities, Expanding Maternal Health Support Across US Cities
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FDA Approves Merck’s GARDASIL 9 for the Prevention of Certain HPV-Related Head and Neck Cancers
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Merck (MRK) Phase 3 KEYNOTE-361 Trial Evaluating KEYTRUDA as Monotherapy and in Combination with Chemotherapy in Patients with Advanced or Metastatic Urothelial Carcinoma Did Not Meet its Primary Endp
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Merck Provides Update on Phase 3 KEYNOTE-361 Trial Evaluating KEYTRUDA® (pembrolizumab) as Monotherapy and in Combination with Chemotherapy in Patients with Advanced or Metastatic Urothelial Carcinom
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Merck (MRK) Announces FDA Approves its RECARBRIO for Treatment of Adults with HABP/VABP
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FDA Approves Merck’s RECARBRIO™ (imipenem, cilastatin, and relebactam) for the Treatment of Adults with Hospital-Acquired and Ventilator-Associated Bacterial Pneumonia (HABP/VABP)
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AstraZeneca (AZN) and Merck (MRK) Announce LYNPARZA Receives Positive Opinion from EU CHMP for First-Line Maintenance Treatment of Patients with gBRCAm
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LYNPARZA® (olaparib) Receives Positive Opinion from EU CHMP for First-Line Maintenance Treatment of Patients with Germline BRCA-Mutated Metastatic Pancreatic Cancer
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KEYTRUDA® (pembrolizumab) plus LENVIMA® (lenvatinib) Combination Demonstrated Clinically Meaningful Tumor Response Rates in Unresectable Hepatocellular Carcinoma and Advanced Renal Cell Carcinoma
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Merck (MRK) Announces KEYTRUDA Superior to Standard of Care Chemotherapy in Patients with MSI-H Colorectal Cancer
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Merck’s KEYTRUDA® (pembrolizumab) Superior to Standard of Care Chemotherapy in Patients with MSI-H Colorectal Cancer
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MilliporeSigma and Baylor College of Medicine Collaborate to Advance a Vaccine Manufacturing Platform to Fight Covid-19
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Merck Announces Third-Quarter 2020 Dividend
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Merck (MRK) Reports Acquisition of Themis
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Merck and Ridgeback Bio Collaborate to Advance Development of Novel Antiviral Candidate, EIDD-2801
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IAVI and Merck Collaborate to Develop Vaccine Against SARS-CoV-2
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Merck to Acquire Themis
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Merck (MRK) will today announce three significant scientific initiatives to combat COVID-19
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Merck to Announce Multiple Scientific Efforts to Combat COVID-19
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Merck (MRK), AstraZeneca (AZN) Report LYNPARZA (olaparib) Approved by FDA for Treatment of HRR Gene-Mutated Metastatic Castration-Resistant Prostate Cancer
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LYNPARZA® (olaparib) Approved by FDA for Treatment of HRR Gene-Mutated Metastatic Castration-Resistant Prostate Cancer That Has Progressed Following Prior Treatment with Enzalutamide or Abiraterone
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Infectious Disease Connect and ILÚM Health Solutions Combine to Advance Precision Treatment of Infectious Diseases and Antimicrobial Stewardship
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Merck Announces Appointment of Organon & Co. Chief Financial Officer and Chief Information Officer
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CORRECTING and REPLACING Merck Announces Appointment of Organon & Co. Chief Financial Officer and Chief Information Officer
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Merck to Present at the UBS Virtual Global Healthcare Conference
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Merck (MRK) New Combination Data for KEYTRUDA Demonstrated Clinical Benefit in Stage III NSCLC and Reinforce Long-Term Survival in Metastatic NSCLC
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Merck (MRK) KEYTRUDA Plus Chemotherapy Demonstrated Statistically Significant Improvement in Progression-Free Survival Versus Chemotherapy in Certain Patients with Metastatic Triple-Negative Breast Ca
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Merck's (MRK) KEYTRUDA Superior to Brentuximab Vedotin, a Standard of Care, in Patients With cHL in Head-to-Head Phase 3 Trial
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Merck (MRK) Novel HIF-2α Inhibitor Showed ORR of Nearly 30% in Patients with VHL Disease-Associated Clear Cell Renal Cell Carcinoma
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Merck’s Novel HIF-2α Inhibitor Showed an Objective Response Rate of Nearly 30% in Patients with von Hippel-Lindau (VHL) Disease-Associated Clear Cell Renal Cell Carcinoma

