KEYTRUDA® (pembrolizumab) Shows Overall Response Rates of 73 to 83 Percent, with Complete Response Rates of 27 to 30 Percent, in Heavily Pre-treated Patients with cHL, in Update to Study KN-087
Dateline City:
KENILWORTH, N.J.
Findings Support Initiation of Phase 3 Pivotal Study (KEYNOTE-204) Evaluating KEYTRUDA Versus Brentuximab Vedotin in Relapsed or Refractory cHL
KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada,
today announced the first-time presentation of findings from
KEYNOTE-087, the phase 2 study investigating the use of KEYTRUDA® (pembrolizumab),
the company’s anti-PD-1 therapy, as a monotherapy in patients with
relapsed or refractory classical Hodgkin lymphoma (cHL). These data will
be presented today at the 52nd Annual Meeting of the American
Society of Clinical Oncology (ASCO) in Chicago from 8:00 – 11:30 a.m.
Language:
English
Contact:
MerckMedia:Pamela Eisele, 267-305-3558orAn Phan, 908-255-6325orInvestors:Teri Loxam, 908-740-1986orJustin Holko, 908-740-1879
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Ticker: MRK Exchange: NYSE
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Source: Merck.com - Research and Development News - Category: Pharmaceuticals Tags: Oncology Newsroom Research and Development News Corporate News Latest News #Merck #MRK $MRK ASCO cancer Keytruda MSD Source Type: news