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Merck (MRK) Receives Priority Review from FDA for Second Application for KEYTRUDA Based on Biomarker
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Merck Receives Priority Review from FDA for Second Application for KEYTRUDA® (pembrolizumab) Based on Biomarker, Regardless of Tumor Type
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Merck (MRK) Announces KEYTRUDA Significantly Improved PFS as First-Line Treatment for MSI-H or dMMR Colorectal Cancer
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Merck Announces KEYTRUDA® (pembrolizumab) Significantly Improved Progression-Free Survival as First-Line Treatment for Advanced Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (d
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Merck to Hold First-Quarter 2020 Sales and Earnings Conference Call on April 28
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Medical Professionals Across Merck & Co., Inc., Pfizer Inc., and Eli Lilly and Company Activate to Support Health Systems, First Responders and Patients Amid COVID-19 Pandemic
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Medical Professionals Across Merck & Co., Inc., Pfizer Inc., and Eli Lilly and Company Activate to Support Health Systems, First Responders and Patients Amid COVID-19 Pandemic
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Merck (MRK) Reports Investigational Drug Vericiguat Significantly Reduced the Risk of Composite Endpoint of Heart Failure Hospitalization or Cardiovascular Death
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Investigational Drug Vericiguat Significantly Reduced the Risk of the Composite Endpoint of Heart Failure Hospitalization or Cardiovascular Death, Compared to Placebo, When Given in Combination with A
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Merck to Donate 300,000 Masks to New Jersey for COVID-19 Emergency Response
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Merck Donates a Half a Million Masks to Support COVID-19 Emergency Response in New York City
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Merck Recommends Rejection of TRC Capital’s “Mini-Tender” Offer
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Merck (MRK) Announces Top-Line Results from Phase 3 Trials Evaluating Gefapixant
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Merck Announces Top-Line Results from Phase 3 Trials Evaluating Gefapixant, an Investigational Treatment for Refractory or Unexplained Chronic Cough
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EMD Serono and Pfizer Provide Update on Phase III JAVELIN Head and Neck 100 Study
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Merck (MRK), AstraZeneca (AZN) Report Update on Phase 3 GY004 for Cediranib & LYNPARZA (olaparib) in Platinum-Sensitive Relapsed Ovarian Cancer
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Update on Phase 3 GY004 for Cediranib and LYNPARZA® (olaparib) in Platinum-Sensitive Relapsed Ovarian Cancer
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Scientists from Merck and the Walter and Eliza Hall Institute of Medical Research Discover Novel Class of Candidate Anti Malaria Agents that Block Multiple Stages of the Lifecycle of the Parasite
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MilliporeSigma's New LANEXO™ System to Improve Scientists' Productivity in the Lab
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Merck Announces New Data from Broad HIV Program at CROI 2020
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Merck's (MRK) KEYTRUDA Significantly Improved PSF Compared with Brentuximab Vedotin in Patients with Relapsed or Refractory cHL
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Merck’s KEYTRUDA® (pembrolizumab) Significantly Improved Progression-Free Survival Compared with Brentuximab Vedotin in Patients with Relapsed or Refractory Classical Hodgkin Lymphoma (cHL)
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Merck to Present at the Cowen Health Care Conference
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Merck Receives Complete Response Letter from the US FDA for Supplemental Biologics License Applications (sBLAs) for KEYTRUDA® (pembrolizumab) Six-Week Dosing Schedule
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ERVEBO® (Ebola Zaire Vaccine, Live) Now Registered in Four African Countries, Within 90 Days of Reference Country Approval and WHO Prequalification
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Merck's (MRK) KEYTRUDA in Combination with Chemotherapy Met Primary Endpoint of PFS as First-Line Treatment for mTNBC
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Merck’s KEYTRUDA® (pembrolizumab) in Combination with Chemotherapy Met Primary Endpoint of Progression-Free Survival (PFS) as First-Line Treatment for Metastatic Triple-Negative Breast Cancer (mTNB
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Merck Announces Fourth-Quarter and Full-Year 2019 Financial Results
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Merck (MRK) Announces Spinoff of Women�s Health, Trusted Legacy Brands and Biosimilars Products
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Merck to Focus on Key Growth Pillars Through Spinoff of Women’s Health, Trusted Legacy Brands and Biosimilars Products into New Company (“NewCo”)
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Merck (MRK) Reports FDA Acceptance for sNDA Review for RECARBRIO (imipenem, cilastatin, and relebactam)
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FDA Accepts For Review Supplemental New Drug Application (sNDA) for RECARBRIO™ (imipenem, cilastatin, and relebactam) for the Treatment of Adults with Hospital-Acquired and Ventilator-Associated Bac
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Merck (MRK) Reports Election of Dr. Christine Seidman and Kathy Warden to Board
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Dr. Christine Seidman and Kathy Warden Elected to Merck Board of Directors
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Merck Announces Second-Quarter 2020 Dividend
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Lung Cancer Study Shows Barriers in Patient Access to Care in Europe
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Merck (MRK) Reports FDA Approval of DIFICID (fidaxomicin) to Treat Clostridioides difficile in Children Aged Six Months and Older
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FDA Approves Merck’s DIFICID® (fidaxomicin) to Treat Clostridioides difficile in Children Aged Six Months and Older
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FDA Accepts Regulatory Submission of Supplemental New Drug Application for LYNPARZA® (olaparib) in HRR-Mutated Metastatic Castration-Resistant Prostate Cancer and Grants Priority Review
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Significant Study on Veterinary Wellbeing Reveals Importance of Continued Focus on Personal and Professional Health and Wellbeing Among Veterinarians
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Merck (MRK) Completes Acquisition of ArQule (ARQL)
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Merck Completes Acquisition of ArQule
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Merck (MRK) Announces FDA Approved its KEYTRUDA for Patients With BCG-Unresponsive, High-Risk, NMIBC With CIS With or Without Papillary Tumors
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Patients With BCG-Unresponsive, High-Risk, Non-Muscle Invasive Bladder Cancer With Carcinoma In Situ With or Without Papillary Tumors Who Are Inel
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Merck's (MRK) KEYTRUDA in Combination with Chemotherapy Significantly Improved PFS Compared to Chemotherapy Alone as First-Line Treatment for ES-SCLC
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Merck’s KEYTRUDA® (pembrolizumab) in Combination with Chemotherapy Significantly Improved Progression-Free Survival Compared to Chemotherapy Alone as First-Line Treatment for Extensive Stage Small
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BAVENCIO Significantly Improved Overall Survival in Patients With Locally Advanced or Metastatic Urothelial Carcinoma
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Merck (MRK) Announces Strategic Oncology Collaboration with Taiho and Astex
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Merck Establishes Strategic Oncology Collaboration with Taiho and Astex
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Merck to Hold Fourth-Quarter and Full-Year 2019 Sales and Earnings Conference Call on February 5

