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FDA Approves KEYTRUDA® Plus LENVIMA® Combination for Patients With Certain Types of Advanced Endometrial Carcinoma

FDA Approves KEYTRUDA® Plus LENVIMA® Combination for Patients With Certain Types of Advanced Endometrial Carcinoma
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United statesGregory lubinieckiCourtney ronaldoPeter dannenbaumMelissa moodyJustine mooreVicky makkerOncology clinical researchStatement of merck co incMerck co incSustainable development goalsMerck research laboratoriesDrug administrationEisai incOncology business group at eisaiExchange commission

VERQUVO® Approved in the European Union

VERQUVO® Approved in the European Union
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United statesPeter dannenbaumMelissa moodyRoy baynesBayer agMerck research laboratoriesEuropean commissionMinistry of healthDrug administrationStatement of merck co incExchange commissionMerck co incEuropean unionEuropean approval grantedMerck researchSafety information

Merck Presents New Data from Ongoing Phase 2a Clinical Trial Evaluating the Safety, Tolerability and Pharmacokinetics of Investigational, Once-Monthly, Oral Islatravir for HIV-1 Prevention at IAS 2021

Merck Presents New Data from Ongoing Phase 2a Clinical Trial Evaluating the Safety, Tolerability and Pharmacokinetics of Investigational, Once-Monthly, Oral Islatravir for HIV-1 Prevention at IAS 2021
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United statesJoan buttertonPeter dannenbaumMelissa moodyMerck research laboratoriesStatement of merck co incSociety conferenceExchange commissionMerck co incResearch for prevention conferencePrevention conferenceMerck researchOral study resultsInvestigational islatravirAfrican americanLooking statement

Merck Announces U S FDA Approval of VAXNEUVANCE for the Prevention of Invasive Pneumococcal Disease in Adults 18 Years and Older Caused by 15 Serotypes

Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses for the Serotypes Shared with PCV13 VAXNEUVANCE Elicited Superior Immune Responses for Serotypes 3, 22F and 33F Compared to PCV13, Which Are Major Causes of Disease known as MSD outside the United States and Canada, today announced the U.S. Food and Drug Administration approved VAXNEUVANCE ™ for active immunization for the prevention of … Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses for the Serotypes Shared with PCV13 (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F) VAXNEUVANCE Elicited Superior Immune Responses for Serotypes 3, 22F and 33F Compared to PCV13, Which Are Major Causes of Disease

United statesPeter dannenbaumSteve wanczykMelissa moodyRoy baynesJose cardonaUs centers for diseaseStatement of merck co incMerck co incPfizer incMerck research laboratoriesDrug administrationAdvisory committee on immunization practicesExchange commissionHealth centerIndago research

FDA Approves Expanded Indication for Merck s KEYTRUDA® in Locally Advanced Cutaneous Squamous Cell Carcinoma

FDA Approves Expanded Indication for Merck s KEYTRUDA® in Locally Advanced Cutaneous Squamous Cell Carcinoma
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United statesVicki goodmanCourtney ronaldoPeter dannenbaumMelissa moodyMerck research laboratoriesMerck access programPatient support programDrug administrationStatement of merck co incEastern cooperative oncology groupMerck co incMerck patient support programExchange commissionNow approvedPatients with recurrent