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WHITEHOUSE STATION, N.J.
WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside the United States and Canada,
announced today that the U.S. Food and Drug Administration (FDA) has
designated lambrolizumab (MK-3475) as a Breakthrough Therapy for the
treatment of patients with advanced melanoma. Lambrolizumab is Mercks
investigational antibody therapy targeting Programmed Death receptor
(PD-1) that is currently being evaluated for the treatment of patients
with advanced melanoma, and other tumor types.
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MerckMedia:Caroline Lapppetito, 267-305-7639orInvestors:Carol Ferguson, 908-423-4465orJustin Holko, 908-423-5088
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