Merck (MRK) Announces European Commission Approves KEYTRUDA Plus LENVIMA as First-Line Treatment for Adult Patients With Advanced RCC

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Go back to Merck (MRK) Announces European Commission Approves KEYTRUDA Plus LENVIMA as First-Line Treatment for Adult Patients With Advanced RCC
Merck & Co. (NYSE: MRK) Delayed: 144.17 -0.54 (0.37%)
Previous Close $144.71    52 Week High $65.46 
Open $145.52    52 Week Low $47.97 
Day High $145.90    P/E 98.07 
Day Low $143.82    EPS $1.47 
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