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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Use at an Additional Recommended Dose of 400 mg Every Six Weeks for All Approved Adult Indications
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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KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (
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