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) has
accepted for review the supplemental Biologics License Application
(sBLA) for KEYTRUDA (pembrolizumab), the companys anti-PD-1
therapy, for the treatment of patients with refractory classical Hodgkin
lymphoma (cHL) or for patients who have relapsed after three or more
prior lines of therapy.
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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