Page 9 - Merck Research News Today : Breaking News, Live Updates & Top Stories | Vimarsana

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults

European Commission Approves Merck s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Neoadjuvant Treatment, Then Continued as Monotherapy as Adjuvant Treatment, for Resectable Non-Small Cell Lung Cancer (NSCLC) at High Risk of Recurrence in Adults
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United statesSolange petersExchange commissionEuropean commissionEuropean commission approves merckProduct serviceMerck co incCommittee for medicinal products humanStatement of merck co incCentre hospitalier universitaire vaudoisMerck research laboratoriesNeoadjuvant treatmentThen continuedAdjuvant treatmentResectable non small cell lung cancerHigh risk

FDA Approves Merck s WINREVAIR, a First-in-Class Treatment for Adults with Pulmonary Arterial Hypertension

WINREVAIR on top of background therapy significantly improved exercise capacity and multiple important secondary outcome measures compared to background therapy alone

France generalUnited statesMarc humbertAaron waxmanMatt granatoEliav barrBristol myers squibbMerck research laboratoriesPulmonary hypertension reference centerWorld health organization groupDrug administrationMerck access programPulmonary hypertension associationWorld health organizationBreakthrough therapy designationPulmonary hypertension

FDA Approves Merck s WINREVAIR™ (sotatercept-csrk), a First-in-Class Treatment for Adults with Pulmonary Arterial Hypertension (PAH, WHO* Group 1)

FDA Approves Merck s WINREVAIR™ (sotatercept-csrk), a First-in-Class Treatment for Adults with Pulmonary Arterial Hypertension (PAH, WHO* Group 1)
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United statesFrance generalMatt granatoPeter dannenbaumAaron waxmanMarc humbertJulie cunninghamSteven grazianoEliav barrPulmonary hypertension reference centerExchange commissionPulmonary hypertension associationMerck access programBristol myers squibbWorld health organizationMerck co inc

Merck Announces Plans to Conduct Clinical Trials of a Novel Investigational Multi-Valent Human Papillomavirus (HPV) Vaccine and Single-Dose Regimen for GARDASIL®9

Company reaffirms commitment to reduce the global burden of HPV-related diseases, including certain cancers .

United statesEliav barrMerck co incMerck research laboratoriesExchange commissionStatement of merck co incHuman papillomavirusMerck researchLooking statementSecurities litigation reform actAnnual report

Merck Completes Acquisition of Harpoon Therapeutics, Inc

Merck Completes Acquisition of Harpoon Therapeutics, Inc
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United statesMerck co incStatement of merck co incMerck research laboratoriesExchange commissionDrug administrationHarpoon therapeutics incHarpoon therapeuticsNasdaq stockMerck researchOrphan drug designationLooking statementSecurities litigation reform actAnnual report