KEYTRUDA® (pembrolizumab) is First Medicine to be Made Available to Patients Through U.K. Early Access to Medicines Scheme (EAMS) for Advanced Melanoma
Dateline City:
KENILWORTH, N.J.
EAMS Aims to Give U.K. Patients Access to Promising, Innovative Treatments Prior to European License
KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada,
today announced that the company’s anti-PD-1 therapy, pembrolizumab,
which is marketed in the U.S. under the name KEYTRUDA®, is
the first treatment to be accepted under the U.K.’s new Early Access to
Medicines Scheme (EAMS). Pembrolizumab was accepted under the scheme for
the treatment of advanced melanoma based on the significance of the
early study findings and unmet medical need.
Language:
English
Contact:
MerckMedia Contacts:Pam Eisele, 267-305-3558Claire Mulhearn, 908-236-1118orInvestor Contacts:Joseph Romanelli, 908-740-1986Justin Holko, 908-740-1879
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Ticker: MRK Exchange: NYSE
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Source: Merck.com - Corporate News - Category: Pharmaceuticals Tags: Oncology Newsroom Prescription Medicine News Corporate News Latest News Source Type: news