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FDA Approves Merck's KEYTRUDA (pembrolizumab) as Adjuvant Treatment for Adult and Pediatric (≥12 Years of Age) Patients With Stage IIB or IIC Melanoma Following Complete Resection

04.12.2021 - Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA, Merckโ€™s anti-PD-1 therapy, for the adjuvant treatment of adult and pediatric (12 years and ...
United States Jason Luke Scot Ebbinghaus Statement Of Merck Co Inc Merck Co Inc Merck Patient Support Program

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