Dateline City:
KENILWORTH, N.J.
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 (FDA)
accepted for review the supplemental Biologics License Application
(sBLA) for KEYTRUDA (pembrolizumab), the companys anti-PD-1
therapy, for the treatment of previously treated patients with advanced
microsatellite instability-high (MSI-H) cancer.
Language:
English
Contact:
MerckMedia:Pamela Eisele, 267-305-3558orKim Hamilton, 908-740-1863orInvestors:Teri Loxam, 908-740-1986orAmy Klug, 908-740-1898
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Ticker: MRK Exchange: NYSE
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