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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Reduced Risk of Death by 27% Versus Chemotherapy as First-Line Treatment for Locally Advanced or Metastatic Esophageal Cancer
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Merck (MRK) Reports First-Line Treatment with KEYTRUDA (pembrolizumab) Doubled 5-Yr Survival Rate (31.9%) vs. Chemotherapy (16.3%) in Certain Patients w/ Metastatic NSCLC & PD-LI Turmors
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First-Line Treatment With Merck’s KEYTRUDA® (pembrolizumab) Doubled Five-Year Survival Rate (31.9%) Versus Chemotherapy (16.3%) in Certain Patients With Metastatic Non-Small Cell Lung Cancer Whose
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AstraZeneca (AZN) and Merck (MRK) Announce LYNPARZA Receives Positive Opinion from EU CHMP for Treatment of BRCA1/2 mCRPC
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LYNPARZA® (olaparib) Recommended for Approval in EU by CHMP as First-Line Maintenance Treatment with Bevacizumab for HRD-Positive Advanced Ovarian Cancer
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LYNPARZA® (olaparib) Receives Positive Opinion from EU CHMP for Treatment of BRCA1/2 Metastatic Castration-Resistant Prostate Cancer (mCRPC)
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LYNPARZA Reduced Risk of Death by 31% vs. Enzalutamide or Abiraterone for Men with BRCA1/2 or ATM-Mutated Metastatic Castration Resistant Prostate Cancer Who Progressed Following Enzalutamide or Abira
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LYNPARZA® (olaparib) Reduced the Risk of Death by 31% in BRCA1/2 or ATM-mutated Metastatic Castration-Resistant Prostate Cancer in Phase III Profound Trial
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Merck Presents Promising New Data for Three Investigational Medicines From Diverse and Expansive Oncology Pipeline at ESMO Virtual Congress 2020
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Merck and Eisai Present First-Time Data From Two Studies Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Seven Different Tumor Types at ESMO Virtual Congress 2020
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Merck’s KEYTRUDA® (pembrolizumab) Reduced the Risk of Distant Metastasis or Death by 40% Versus Placebo as Adjuvant Treatment in Resected, High-Risk Stage III Melanoma
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AstraZeneca (AZN), Merck (MRK) Report LYNPARZA Improved Median PFS to Over Four and a Half Years Compared to 13.8 Months with Placebo for Patients with BRCA-Mutated Advanced Ovarian Cancer
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LYNPARZA® (olaparib) Improved Median Progression-Free Survival to Over Four and a Half Years Compared to 13.8 Months with Placebo for Patients with BRCA-Mutated Advanced Ovarian Cancer
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Pfizer (PFE), Merck (MRK) Biopharmaceutical Business, EMD Serono, Reports Publication of BAVENCIO Pivotal Phase III JAVELIN Bladder 100 Results
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BAVENCIO Pivotal Phase III JAVELIN Bladder 100 Results Published in The New England Journal of Medicine
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Merck to Hold Investor Briefing Following ESMO Virtual Congress 2020
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Merck to Present at the 2020 Cantor Fitzgerald Virtual Global Healthcare Conference
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Seattle Genetics (SGEN) and Merck (MRK) Announce Two Strategic Oncology Collaborations; Merck to Invest $1B
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Seattle Genetics and Merck Announce Two Strategic Oncology Collaborations
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Merck to Present at the Morgan Stanley 18th Annual Virtual Global Healthcare Conference
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MilliporeSigma Announces $65 Million Antibody-Drug Conjugate Manufacturing Expansion
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/C O R R E C T I O N -- MilliporeSigma/
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Merck (MRK) Announces Positive Topline Results from Two Phase 3 Adult Studies Evaluating V114, Investigational 15-valent Pneumococcal Conjugate Vaccine, Including Pivotal Trial
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Merck Announces Positive Topline Results from Two Phase 3 Adult Studies Evaluating V114, Merck’s Investigational 15-valent Pneumococcal Conjugate Vaccine, Including Pivotal Trial
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Merck's (MRK) Gefapixant Significantly Decreased Cough Frequency Compared to Placebo at Week 12 and 24 in Patients with Refractory or Unexplained Chronic Cough
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Merck’s Gefapixant (45 mg Twice Daily) Significantly Decreased Cough Frequency Compared to Placebo at Week 12 and 24 in Patients with Refractory or Unexplained Chronic Cough
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Vaccine makers announce pledge, outlining united commitment to uphold integrity of scientific process
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Biopharma Leaders Unite to Stand With Science
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Biopharma Leaders Unite to Stand with Science
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Biopharma Leaders Unite To Stand With Science
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Biopharma Leaders Unite to Stand with Science
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Biopharma Leaders Unite to Stand with Science
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Merck to Present at the Citi 15th Annual BioPharma Virtual Conference
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Merck (MRK) Says New Scientific Data at the ESMO Virtual Congress 2020 Reflect its Commitment to Advancing Cancer Research and Care
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New Scientific Data at the ESMO Virtual Congress 2020 Reflect Merck’s Commitment to Advancing Cancer Research and Care
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Merck's (MRK) KEYTRUDA Receives Two New Approvals in Japan
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Merck’s KEYTRUDA® (pembrolizumab) Receives Two New Approvals in Japan
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Merck's (MRK) KEYTRUDA in Combination With Chemotherapy Significantly Improved OS and PFS Compared With Chemotherapy in Locally Advanced or First-Line Metastatic Esophageal Cancer
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Merck’s KEYTRUDA® (pembrolizumab) in Combination With Chemotherapy Significantly Improved Overall Survival and Progression-Free Survival Compared With Chemotherapy in Locally Advanced or First-Line
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Merck Animal Health Completes Acquisition of IdentiGEN
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Merck and Hanmi Pharmaceutical Enter into Licensing Agreement to Develop Efinopegdutide, an Investigational Once-Weekly Therapy for Nonalcoholic Steatohepatitis (NASH)
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Merck (MRK) Animal Health Completes Acquisition of Worldwide Rights to VECOXAN Brand of Parasiticides for Ruminant Portfolio
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Merck Animal Health Completes Acquisition of Worldwide Rights to VECOXAN® Brand of Parasiticides for Ruminant Portfolio
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Merck Announces Second-Quarter 2020 Financial Results
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Merck (MRK) Announces Two US Regulatory Milestones for KEYTRUDA in Triple-Negative Breast Cancer
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Merck Announces Two US Regulatory Milestones for KEYTRUDA® (pembrolizumab) in Triple-Negative Breast Cancer (TNBC)
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Merck (MRK) Announces FDA Grants Breakthrough Therapy Designation to Novel HIF-2α Inhibitor MK-6482 for Treatment of Certain Patients With VHL- Associated RCC
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FDA Grants Breakthrough Therapy Designation to Merck’s Novel HIF-2α Inhibitor MK-6482 for Treatment of Certain Patients With Von Hippel-Lindau Disease- Associated Renal Cell Carcinoma
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Merck Announces Fourth-Quarter 2020 Dividend
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Factbox: More companies join Facebook ad boycott bandwagon

