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United statesNew jerseyCourtney ronaldoSteven grazianoJulie cunninghamPeter dannenbaumJennifer zacharyUs district courtPatent officeExchange commissionMerck co incStatement of merck co incPatent term extensionLooking statementSecurities litigation reform actAnnual report

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New jerseyUnited statesCourtney ronaldoPeter dannenbaumSteven grazianoJennifer zacharyJulie cunninghamStatement of merck co incPatent officeUs district courtMerck co incExchange commissionPatent term extensionLooking statementSecurities litigation reform actAnnual report

Merck to Present Data for Efinopegdutide (MK-6024), an Investigational GLP-1/Glucagon Receptor Co-agonist, in Patients with Nonalcoholic Fatty Liver Disease (NAFLD) at EASL 2023

Merck to Present Data for Efinopegdutide (MK-6024), an Investigational GLP-1/Glucagon Receptor Co-agonist, in Patients with Nonalcoholic Fatty Liver Disease (NAFLD) at EASL 2023
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United statesCourtney ronaldoSam engelSteven grazianoPeter dannenbaumJulie cunninghamExchange commissionMerck research laboratoriesDrug administrationStatement of merck co incMerck co incFast track designationNonalcoholic steatohepatitisEuropean associationAnnual congressMerck research

FDA Accepts Application for Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer

Acceptance based on results from the Phase 3 KEYNOTE-966 trial, which showed a significant overall survival benefit in these patientsRAHWAY, N.J. (BUSINESS WIRE) $MRK #MRK Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has accep.

United statesDamini chokshiMichael mcardlePeter dannenbaumJulie cunninghamScot ebbinghausAmerican association for cancer researchMerck research laboratoriesDrug administrationBiologics license applicationAmerican associationCancer researchPrescription drug user fee actMerck researchSelected important safetyImportant safety information

Merck (MRK) Announces FDA Acceptance of Application for KEYTRUDA Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer

Merck (MRK) Announces FDA Acceptance of Application for KEYTRUDA Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer
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United statesMichael mcardleScot ebbinghausJulie cunninghamDamini chokshiPeter dannenbaumAmerican association for cancer researchDrug administrationExchange commissionMerck co incStatement of merck co incMerck research laboratoriesBiologics license applicationAmerican associationCancer researchPrescription drug user fee act