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 AdultsBusiness Wire • 03/28/24
Merck shares move higher as lung disorder drug secures ‘squeaky clean' label from FDAProactive Investors • 03/27/24
Merck's stock rallies toward a record after FDA OKs arterial-hypertension drugMarket Watch • 03/27/24
FDA Approves Merck's WINREVAIR™ (sotatercept-csrk), a First-in-Class Treatment for Adults with Pulmonary Arterial Hypertension (PAH, WHO* Group 1)Business Wire • 03/26/24
Merck's Cardiovascular 'Renaissance' Is Here With The First Approval Of A $10 Billion FranchiseInvestors Business Daily • 03/26/24
Merck's (MRK) Keytruda-Lynparza Combo Fails 2nd Lung Cancer StudyZacks Investment Research • 03/22/24
Merck Provides Update on Phase 3 KEYLYNK-006 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus Maintenance LYNPARZA® (olaparib) for Certain Patients With Metastatic Nonsquamous Non-Small Cell Lung CancerBusiness Wire • 03/21/24
Koneksa Announces Merck Joins Data Syndication Partnership Program Around Parkinson's Digital Biomarkers Observational StudyBusiness Wire • 03/20/24
Merck Announces Positive Data on V116, an Investigational, 21-Valent Pneumococcal Conjugate Vaccine Specifically Designed for Adults, Demonstrated Immune Responses in AdultsBusiness Wire • 03/19/24
FarmSee Ltd Announces the Completion of a Minority Investment in its Swine Monitoring PlatformPRNewsWire • 03/15/24