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Merck Announces Phase 3 KEYNOTE-671 Trial Met Primary Endpoint of Event-Free Survival (EFS) in Patients With Resectable Stage II, IIIA or IIIB Non-Small Cell Lung Cancer
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Merck (MRK) Issues Update on Phase 3 Trials KEYNOTE-641 and KEYNOTE-789
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Merck Provides Update on Phase 3 Trials KEYNOTE-641 and KEYNOTE-789
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Merck (MRK) and Ridgeback Provide Update on EU Marketing Authorization Application for LAGEVRIO
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Merck and Ridgeback Provide Update on EU Marketing Authorization Application for LAGEVRIO™ (Molnupiravir)
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Merck (MRK) Opens Enrollment in New Phase 3 Trials with Once-Daily Islatravir in Combination with Doravirine for Treatment of HIV-1 Infection
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Merck Opens Enrollment in New Phase 3 Clinical Trials with Investigational Once-Daily Islatravir in Combination with Doravirine for Treatment of HIV-1 Infection
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Merck to Present New Data for Sotatercept and MK-0616 at ACC.23/WCC, Demonstrating Significant Progress in Advancing Its Innovative Cardiovascular Pipeline
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Merck (MRK) Provides Update on Phase 3 MOVe-AHEAD Trial Evaluating LAGEVRIO
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Merck Provides Update on Phase 3 MOVe-AHEAD Trial Evaluating LAGEVRIO™ (molnupiravir) for Post-exposure Prophylaxis for Prevention of COVID-19
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Merck (MRK) Announces FDA Acceptance for Priority Review of sNDA for PREVYMIS in Cytomegalovirus Disease in Kidney Transplant Recipients
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U.S. FDA Accepts for Priority Review the Supplemental New Drug Application for Merck’s PREVYMIS™ for Prophylaxis of Cytomegalovirus Disease in Kidney Transplant Recipients at High Risk
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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Significantly Improved Overall Survival Versus Chemotherapy Alone in Patients With HER2-Negative Gastric or Gastroesophageal Junction (GEJ) Adeno
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Merck (MRK) and AstraZeneca (AZN) Present Final Results of Key Secondary Overall Survival Endpoint From Phase 3 PROpel Trial
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Merck and AstraZeneca Present Final Results of Key Secondary Overall Survival Endpoint From Phase 3 PROpel Trial at 2023 American Society of Clinical Oncology Genitourinary Cancers Symposium
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Merck (MRK) Reports KEYTRUDA Plus Chemotherapy Met Primary Endpoint of Progression-Free Survival (PFS) as First-Line Therapy for Advanced or Recurrent Endometrial Carcinoma
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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Met Primary Endpoint of Progression-Free Survival (PFS) as First-Line Therapy for Advanced or Recurrent Endometrial Carcinoma
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Merck Announces Fourth-Quarter and Full-Year 2022 Financial Results
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Merck (MRK) Announces FDA Approval of KEYTRUDA as Adjuvant Treatment Following Surgical Resection and Platinum-Based Chemotherapy for Patients With Stage IB, II, or IIIA (NSCLC)
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FDA Approves KEYTRUDA® (pembrolizumab) as Adjuvant Treatment Following Surgical Resection and Platinum-Based Chemotherapy for Patients With Stage IB (T2a ≥4 Centimeters), II, or IIIA Non-Small Cell
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Merck Animal Health Receives U.S. FDA Approval of Expanded Indication for BRAVECTO (fluralaner) Chews for Dogs
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Merck (MRK) Announces KEYNOTE-991 Trial Evaluating KEYTRUDA Plus Enzalutamide and Androgen Deprivation Therapy
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Merck Announces KEYNOTE-991 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus Enzalutamide and Androgen Deprivation Therapy in Patients With Metastatic Hormone-Sensitive Prostate Cancer to Stop for Fut
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Merck's (MRK) KEYTRUDA Plus Chemotherapy Significantly Improved Overall Survival in KEYNOTE-966 Trial
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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Significantly Improved Overall Survival Versus Chemotherapy in First-Line Advanced or Unresectable Biliary Tract Cancer in KEYNOTE-966 Trial
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Merck Announces Second-Quarter 2023 Dividend
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Merck (MRK) completes takeover of Imago BioSciences
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Merck Completes Tender Offer to Acquire Imago BioSciences, Inc.
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Merck Named One of America’s Most JUST Companies by JUST Capital and CNBC, Industry Leader in Pharmaceuticals and Biotech
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Merck to Hold Fourth-Quarter and Full-Year 2022 Sales and Earnings Conference Call February 2
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Merck to Present at the 41st Annual J.P. Morgan Healthcare Conference
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Merck to Present at the Goldman Sachs Healthcare CEOs Unscripted Conference
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Merck (MRK) and Kelun-Biotech Enter Deal for Seven Investigational Antibody-drug Conjugate Cancer Candidates
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Merck and Kelun-Biotech Announce Exclusive License and Collaboration Agreement for Seven Investigational Antibody-drug Conjugate Candidates for the Treatment of Cancer
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LYNPARZA® (olaparib) in Combination With Abiraterone and Prednisone or Prednisolone Approved in the EU as Treatment for Certain Patients With Metastatic Castration-Resistant Prostate Cancer
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Merck (MRK), Seagen (SGEN) and Astellas Announce FDA Acceptance of sBLA for PADCEV with KEYTRUDA
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Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line Treatment of Certain Patients With Locally Advance
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Astellas, Seagen and Merck Announce FDA Acceptance of Supplemental Biologics License Applications for PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line Treatment of
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AstraZeneca and Merck Provide Update on US Regulatory Review of LYNPARZA® (olaparib) in Combination With Abiraterone and Prednisone or Prednisolone as Treatment of Metastatic Castration-Resistant Pro
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Merck Begins Tender Offer to Acquire Imago BioSciences, Inc.
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MilliporeSigma Gains Leading Perfusion Micro-Bioreactor with Erbi Biosystems Acquisition
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Merck to Present Data From Its Hematology Portfolio and Promising Pipeline at the 64th American Society of Hematology (ASH) Annual Meeting
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Merck Announces First-Quarter 2023 Dividend
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Merck (MRK) Announces Phase 3 KEYNOTE-859 Trial Met Primary Endpoint
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Merck Announces Phase 3 KEYNOTE-859 Trial Met Primary Endpoint of Overall Survival in Patients With HER2-Negative Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma
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Disney, Imago BioSciences rise premarket; Coinbase, Carvana fall
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Merck (MRK) Acquires Imago BioSciences (IMGO) for $36/sh or $1.35B
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Merck to Present at the 5th Annual Evercore ISI HealthCONx Conference
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Merck to Acquire Imago BioSciences, Inc.
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MilliporeSigma Invests $ 286 Million in U.S. Drug Safety Testing Capacity

