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Merck (MRK) Q3 2023 Earnings Call Transcript

MRK earnings call for the period ending September 30, 2023.

United statesLouise chen cantor fitzgeraldChris schottCaroline litchfieldAndrew baum citiMara goldsteinJonathan cohenHelen hobbsGeoff meachamSteve scalaAmerica merrill lynchChris shibutani goldman sachsMohit bansalTerence flynnAndrew baumSeamus fernandez

KEYTRUDA® (pembrolizumab) Plus Trastuzumab and Chemotherapy Significantly Improved Progression-Free Survival (PFS) Versus Trastuzumab and Chemotherapy in First-Line HER2-Positive Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma

In the KEYNOTE-811 trial, the KEYTRUDA regimen demonstrated a statistically significant PFS improvement in advanced HER2-positive gastric or GEJ adenocarcinoma in tumors expressing PD-L1 compared to.

United statesYelenay janjigianMerck co incEuropean commissionExchange commissionDrug administrationMemorial sloan kettering cancer centerStatement of merck co incEuropean society for medical oncologyMerck research laboratoriesEuropean societyMedical oncologyCombined positive scoreChief attending physicianGastrointestinal oncologyPrincipal investigator

Prevymis: Merck s viral infection drug gets EU recommendation – The Frontier Post

Prevymis: Merck s viral infection drug gets EU recommendation – The Frontier Post
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Bruxelles capitaleElizabeth rheeCommittee for medicinal products human useEuropean unionMerck coMerck research laboratoriesDrug administrationEuropean medicines agencyMerck researchMedicinal productsHuman use

Merck (MRK) Announces FDA Approval of KEYTRUDA for Treatment of Patients With Resectable NSCLC in Combination With Chemotherapy

Merck (MRK) Announces FDA Approval of KEYTRUDA for Treatment of Patients With Resectable NSCLC in Combination With Chemotherapy
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United statesJulie cunninghamPeter dannenbaumDamini chokshiHeather wakeleePatient support programAmerican joint committee on cancerMerck access programMerck co incEuropean society for medical oncologyMerck patient support programMerck research laboratoriesStanford universityDrug administrationExchange commissionStatement of merck co inc

FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery

FDA Approves KEYTRUDA® (pembrolizumab) for Treatment of Patients With Resectable (T?4 cm or N+) NSCLC in Combination With Chemotherapy as Neoadjuvant Treatment, Then Continued as a Single Agent as Adjuvant Treatment After Surgery
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United statesHeather wakeleeStanford universityDrug administrationMerck co incEuropean society for medical oncologyProduct serviceMerck access programPatient support programStatement of merck co incExchange commissionMerck research laboratoriesAmerican joint committee on cancerMerck patient support programPatients with resectableNeoadjuvant treatment