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Merck (MRK) Announces Phase 3 KEYNOTE-671 Trial Met Primary Endpoint of Event-Free Survival (EFS)

Merck (MRK) Announces Phase 3 KEYNOTE-671 Trial Met Primary Endpoint of Event-Free Survival (EFS)
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Merck Provides Update on Phase 3 Trials KEYNOTE-641 and KEYNOTE-789

28.02.2023 - Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today provided updates on two Phase 3 trials, KEYNOTE-641 and KEYNOTE-789. Merck is discontinuing the Phase 3 KEYNOTE-641 trial evaluating KEYTRUDA (pembrolizumab), Merck’s .

United statesEliav barrMerck research laboratoriesStatement of merck co incExchange commissionMerck co incMerck researchProstate cancer workingSelected important safetyImportant safety informationFatal immune mediated adverseWhich can present with diabeticNervous systemPatients with multipleNeck squamous cellBacillus calmette guerin unresponsive

Merck (MRK) Issues Update on Phase 3 Trials KEYNOTE-641 and KEYNOTE-789

Merck (MRK) Issues Update on Phase 3 Trials KEYNOTE-641 and KEYNOTE-789
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United statesJulie cunninghamNikki sullivanPeter dannenbaumEliav barrDamini chokshiMerck research laboratoriesData monitoring committeeStatement of merck co incExchange commissionMerck co incWall streetData monitoringMerck researchProstate cancer working group modifiedSelected important safety

Moderna, Inc : Moderna and Merck Announce mRNA-4157/V940, an Investigational Personalized mRNA Cancer Vaccine, in Combination With KEYTRUDA , was Granted Breakthrough Therapy Designation by the FDA for Adjuvant Treatment of Patients With High-Risk Melanom

Designation based on positive data from Phase 2b KEYNOTE-942/mRNA-4157-P201 trialCAMBRIDGE, MA and RAHWAY, NJ / ACCESSWIRE / February 22, 2023 / Moderna, Inc. (NASDAQ:MRNA), a biotechnology company pioneering

United statesUnited kingdomLavina talukdarErich rubinJulie cunninghamDennis riedlMary beth woodinDamini chokshiJustine mooreStephen hogePeter dannenbaumMerck research laboratoriesDrug administrationStatement of merck co incExchange commissionMerck co inc

Moderna and Merck Announce mRNA-4157/V940, an Investigational Personalized mRNA Cancer Vaccine, in Combination With KEYTRUDA(R) (pembrolizumab), was Granted Breakthrough Therapy Designation by the FDA

Moderna and Merck Announce mRNA-4157/V940, an Investigational Personalized mRNA Cancer Vaccine, in Combination With KEYTRUDA(R) (pembrolizumab), was Granted Breakthrough Therapy Designation by the FDA
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United statesUnited kingdomLavina talukdarErich rubinJulie cunninghamMary beth woodinDamini chokshiJustine mooreStephen hogePeter dannenbaumMerck research laboratoriesDrug administrationStatement of merck co incExchange commissionMerck co incModerna inc