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Merck (MRK) Completes Acquisition of Pandion Therapeutics (PAND)
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Merck Completes Acquisition of Pandion Therapeutics
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Merck (MRK) Announces Acquisition of Alydia Health on behalf of its Planned Spinoff of Organon
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Merck Announces Acquisition of Alydia Health on behalf of its Planned Spinoff of Organon
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Merck (MRK) Receives Positive EU CHMP Opinion for Updated Label of KEYTRUDA To Include Results of Phase 3 KEYNOTE-361 Trial in Certain Adult Patients with Locally Advanced or Metastatic Urothelial Can
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Merck Receives Positive EU CHMP Opinion for Updated Label of KEYTRUDA® (pembrolizumab) To Include Results of Phase 3 KEYNOTE-361 Trial in Certain Adult Patients with Locally Advanced or Metastatic Ur
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Merck (MRK) Receives CRL From US FDA for Supplemental Biologics License Application for KEYTRUDA in High-Risk Early-Stage TNBC
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Merck Receives Complete Response Letter From US FDA for Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) in High-Risk Early-Stage Triple-Negative Breast Cancer (TNBC)
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Merck to Hold First-Quarter 2021 Sales and Earnings Conference Call on April 29
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Merck (MRK) Appoints Caroline Litchfield as CFO
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Merck Appoints Caroline Litchfield Chief Financial Officer
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FDA Approves Merck’s (MRK) KEYTRUDA Plus Platinum- and Fluoropyrimidine-Based Chemotherapy for Treatment of Certain Patients With Locally Advanced or Metastatic Esophageal or GEJ Carcinoma
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) Plus Platinum- and Fluoropyrimidine-Based Chemotherapy for Treatment of Certain Patients With Locally Advanced or Metastatic Esophageal or Gastroesoph
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Merck (MRK) Announces KEYTRUDA Plus LENVIMA Significantly Improved PFS and OS Versus Chemotherapy in Patients With Advanced Endometrial Cancer
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KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) Significantly Improved Progression-Free Survival and Overall Survival Versus Chemotherapy in Patients With Advanced Endometrial Cancer Following
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Merck (MRK) Files Form 10 Related to Planned Spinoff of Organon & Co.
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Merck Announces Filing of Form 10 Registration Statement in Connection with Planned Spinoff of Organon & Co.
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MilliporeSigma Accelerates European Expansion Plans for Single-use Products Critical to Manufacturing Vaccines and Lifesaving Therapies
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EC Approves Expanded Indication for Merck’s (MRK) KEYTRUDA in Adult and Pediatric Patients With Relapsed or Refractory Classical Hodgkin Lymphoma
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European Commission Approves Expanded Indication for Merck’s KEYTRUDA® (pembrolizumab) in Adult and Pediatric Patients With Relapsed or Refractory Classical Hodgkin Lymphoma (cHL)
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Mike Nally to Leave Merck; Frank Clyburn to Lead All Merck Human Health
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Merck (MRK) Receives Priority Review From FDA for New Drug Application for HIF-2α Inhibitor Belzutifan
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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

