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Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Gemcitabine and Cisplatin as First-Line Treatment for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Merck & Co , Inc : Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Gemcitabine and Cisplatin as First-Line Treatment for Locally Advanced Unresectable or Metastatic Biliary Tract Cancer
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United statesDamini chokshiPeter dannenbaumMichael mcardleJulie cunninghamDrug administrationMerck research laboratoriesMerck co incExchange commissionEuropean unionStatement of merck co incEuropean commissionEuropean medicines agencyMedicinal productsHuman useMarjorie green

KEYTRUDA® (pembrolizumab) Significantly Improved Overall Survival (OS) Versus Placebo as Adjuvant Therapy for Certain Patients With Renal Cell Carcinoma (RCC) Following Nephrectomy

KEYTRUDA® (pembrolizumab) Significantly Improved Overall Survival (OS) Versus Placebo as Adjuvant Therapy for Certain Patients With Renal Cell Carcinoma (RCC) Following Nephrectomy
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United statesPeter dannenbaumMichael mcardleJulie cunninghamDamini chokshiStatement of merck co incMerck research laboratoriesData monitoring committeeEuropean society for medical oncologyExchange commissionAmerican society of clinical oncology annual meetingMerck co incEuropean unionEuropean societyMedical oncologyMarjorie green

KEYTRUDA® (pembrolizumab) Significantly Improved Overall Survival (OS) Versus Placebo as Adjuvant Th

KEYTRUDA is the first therapy to show a statistically significant improvement in OS as adjuvant therapy in patients with RCC at a higher risk of recurrence following nephrectomyNew OS results build on the significant disease-free survival benefit previously reported from the KEYNOTE-564 trialRAHWAY, N.J. (BUSINESS.

United statesPeter dannenbaumJulie cunninghamMichael mcardleDamini chokshiMerck research laboratoriesAmerican society of clinical oncology annual meetingData monitoring committeeEuropean society for medical oncologyEuropean unionEuropean societyMedical oncologyMarjorie greenMerck researchClinical oncology annual meetingSelected important safety

FDA Approves Merck s KEYTRUDA® (pembrolizumab) Plus Gemcitabine and Cisplatin as Treatment for Patients With Locally Advanced Unresectable or Metastatic Biliary Tract Cancer

Approval based on results from the Phase 3 KEYNOTE-966 trial, which demonstrated significant overall survival benefit in these patients versus chemotherapy aloneApproval marks sixth gastrointestinal cancer indication for KEYTRUDA-based regimens in the USRAHWAY, N.J. (BUSINESS WIRE) $MRK #MRK Merck (NYSE: MRK), kn.

United statesSan franciscoMichael mcardleDamini chokshiJulie cunninghamPeter dannenbaumRobin kate kelleyUniversity of californiaDrug administrationMerck research laboratoriesImportant safetyMarjorie greenMerck researchSelected important safetyImportant safety informationFatal immune mediated adverse

KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Reduced Risk of Death by More Than Half Versus Chemotherapy in Patients With Previously Untreated Locally Advanced or Metastatic Urothelial Cancer

KEYTRUDA plus enfortumab vedotin significantly prolonged overall survival by 53% - an improvement in median OS of more than 15 months - compared to chemotherapy in the total patient.

United statesSeagen padcevMerck co incSeagen incAgensys incStatement of merck co incExchange commissionResponse evaluation criteriaSolid tumorsBacillus calmette guerinSelected important safetyImportant safety informationFatal immune mediated adverseWhich can present with diabeticNervous systemConnective tissue