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European Commission Approves KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) as First-Line Treatment for Adult Patients With Advanced Renal Cell Carcinoma
Merck & Company, Inc. (new) (MRK)
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Source: Business Wire
Last merck & company, inc. (new) earnings: 4/28 06:45 am
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US:NYSE Investor Relations: investors.merck.com/home/default.aspx
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Approval Based on Results From CLEAR/KEYNOTE-581 Trial Demonstrating KEYTRUDA Plus LENVIMA Significantly Reduced the Risk of Disease Progression or Death by 61%, With a
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