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Merck Receives Priority Review From FDA for New Drug Application for HIF-2α Inhibitor Belzutifan (MK-6482)
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Merck to Host Investor Briefing to Discuss Broad HIV Development Program and Newly Announced Collaboration with Gilead
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Gilead (GILD), Merck (MRK) Announce Agreement to Jointly Develop and Commercialize Long-Acting, Investigational Treatment Combinations of Lenacapavir and Islatravir in HIV
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Gilead and Merck Announce Agreement to Jointly Develop and Commercialize Long-Acting, Investigational Treatment Combinations of Lenacapavir and Islatravir in HIV
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Merck (MRK) Presents Results from Phase 1 Trial Evaluating Investigational Islatravir Subdermal Implant for the Prevention of HIV-1 Infection at CROI 2021
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Merck Presents Results from Phase 1 Trial Evaluating Investigational Islatravir Subdermal Implant for the Prevention of HIV-1 Infection at CROI 2021
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Ridgeback Biotherapeutics and Merck Announce Preliminary Findings from a Phase 2a Trial of Investigational COVID-19 Therapeutic Molnupiravir
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Merck (MRK) Begins Tender Offer to Acquire Pandion Therapeutics (PAND)
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Merck Begins Tender Offer to Acquire Pandion Therapeutics
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Merck to Present at the Barclays Global Healthcare Conference
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Merck to Present New Data from Various HIV Research and Development Programs at CROI 2021
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Merck (MRK) Confirms It Will Help Produce Johnson & Johnson’s (JNJ) COVID-19 Vaccine;
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Merck to Help Produce Johnson & Johnson’s COVID-19 Vaccine; BARDA to Provide Merck With Funding to Expand Merck’s Manufacturing Capacity for COVID-19 Vaccines and Medicines
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Merck Announces Fifth Round of Global Grants to Tackle Maternal Mortality and Promote Health Equity Worldwide
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Merck (MRK) Provides Update on KEYTRUDA Indication in Metastatic Small Cell Lung Cancer in the US
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Merck Provides Update on KEYTRUDA® (pembrolizumab) Indication in Metastatic Small Cell Lung Cancer in the US
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Merck (MRK) Announces U.S. FDA Accepts its Gefapixant New Drug Application for Review
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U.S. FDA Accepts Merck’s Gefapixant New Drug Application for Review
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Merck Animal Health Completes Acquisition of Poultry Sense Limited
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Merck (MRK) to Acquire Pandion Therapeutics (PAND) for $60/Share in $1.85 Billion Deal
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Merck to Acquire Pandion Therapeutics
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Merck to Present at the Cowen 41st Annual Health Care Conference
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AstraZeneca (AZN), Merck (MRK) Announce IDMC Concludes OlympiA Trial of LYNPARZA Crossed Superiority Boundary for Invasive Disease-Free Survival vs. Placebo at Planned Interim Analysis
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Independent Data Monitoring Committee Concludes OlympiA Trial of LYNPARZA® (olaparib) Crossed Superiority Boundary for Invasive Disease-Free Survival vs. Placebo at Planned Interim Analysis
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KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Demonstrated Superior Progression-Free Survival (PFS) and Overall Survival (OS) Versus Sunitinib as First-Line Treatment for Patients With Advanc
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Merck Announces Fourth-Quarter and Full-Year 2020 Financial Results
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Merck (MRK) CEO Kenneth C. Frazier to Retire; Board Elects Robert M. Davis as Successor; Frazier to Continue as Executive Chairman
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Kenneth C. Frazier to Retire as Merck CEO; Board Elects Robert M. Davis as Successor; Frazier to Continue as Executive Chairman
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Merck (MRK) Reports Election of Dr. Stephen Mayo to Board
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Dr. Stephen Mayo Elected to Merck Board of Directors
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Merck (MRK) Announces Positive EU CHMP Opinion for Expanded Approval of KEYTRUDA (pembrolizumab) in Certain Patients with R/R Classical Hodgkin Lymphoma
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Merck (MRK) Reports Results from Head-to-Head Phase 3 KEYNOTE-598 Trial Evaluating KEYTRUDA (pembrolizumab) in Combination With Ipilimumab (Yervoy)
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Merck Receives Positive EU CHMP Opinion for Expanded Approval of KEYTRUDA® (pembrolizumab) in Certain Patients With Relapsed or Refractory Classical Hodgkin Lymphoma
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Merck Presents Results From Head-to-Head Phase 3 KEYNOTE-598 Trial Evaluating KEYTRUDA® (pembrolizumab) in Combination With Ipilimumab Versus KEYTRUDA Monotherapy in Certain Patients With Metastatic
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Merck Announces Second Cohort of Safer Childbirth Cities Organizations Committed to Improving Maternal Health Equity and Reducing Preventable Maternal Deaths in the US
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Merck Announces Second-Quarter 2021 Dividend
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Merck (MRK) Presents Interim Findings from Phase 2a Clinical Trial Evaluating Investigational Once-Monthly Oral Islatravir for the Prevention of HIV-1 Infection at HIVR4P 2021
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Merck Presents Interim Findings from Phase 2a Clinical Trial Evaluating Investigational Once-Monthly Oral Islatravir for the Prevention of HIV-1 Infection at HIVR4P 2021
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Merck (MRK) Reports EC Approves KEYTRUDA (pembrolizumab) as First-Line Treatment in Adult Patients with MSI-H or dMMR Colorectal Cancer
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European Commission Approves KEYTRUDA® (pembrolizumab) as First-Line Treatment in Adult Patients With Metastatic Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Colorectal
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Merck (MRK) Discontinues Development of SARS-CoV-2/COVID-19 Vaccine Candidates
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Merck Discontinues Development of SARS-CoV-2/COVID-19 Vaccine Candidates; Continues Development of Two Investigational Therapeutic Candidates
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European Commission Approves BAVENCIO® (avelumab) for First-Line Maintenance Treatment of Locally Advanced or Metastatic Urothelial Carcinoma
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Merck (MRK) Announces U.S. FDA Approval of VERQUVO
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Merck Announces U.S. FDA Approval of VERQUVO® (vericiguat)
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Merck (MRK) Announces FDA Accepts for Priority Review the BLA for V114, its Investigational 15-valent Pneumococcal Conjugate Vaccine, for Use in Adults 18 Years of Age and Older
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U.S. FDA Accepts for Priority Review the Biologics License Application for V114, Merck’s Investigational 15-valent Pneumococcal Conjugate Vaccine, for Use in Adults 18 Years of Age and Older
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Merck to Hold Fourth-Quarter and Full-Year 2020 Sales and Earnings Conference Call on February 4
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MilliporeSigma Acquires AmpTec to Expand mRNA Capabilities for Vaccines, Treatments and Diagnostics
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Merck to Present at the 39th Annual J.P. Morgan Healthcare Conference

