European Medicines Agency ’s CHMP Recommends Merck’s KEYTRUDA® (pembrolizumab) for the First-Line Treatment of Patients with Metastatic Non-Small Cell Lung Cancer (NSCLC) Whose Tumors Have High PD-L1 Expression with No EGFR or ALK Positive Tumor...
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KENILWORTH, N.J. Opinion Based on Findings from KEYNOTE-024 Trial, Which Showed Superior Overall Survival and Progression Free Survival with KEYTRUDA Compared to Chemotherapy First Anti-PD-1 Therapy to Receive a CHMP Positive Opinion for Previously Untreated Patients with Metastatic NSCLCKENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada,
announced today that the Committee for Medicinal Products for Human Use
(CHMP) of the European Medicines Agency (EMA) has adopted a positive
opinion recommending approval of KEYTRUDA ® (pembrolizumab), the
company’s anti-PD-1 therapy, for the first-line treatment of metastatic
non-small cell lung cancer (NSCLC) in adults whose tumors have high
PD-L1 expression (tumor proportion score [TPS] of 50 percent or more)
with no EGFR or ALK positive tuLanguage:
EnglishContact: MerckMedia:Pamela Eisele, 267-305-3558Courtney Ronaldo, 908-236-1108orInvestors:Teri Loxam, 908-740-1986Amy Klug, 908-740-1898Ticker Slug:Ticker:MRKExchange:NYSE
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Source: Merck.com - Corporate News - Category: Pharmaceuticals Tags: Oncology Newsroom Prescription Medicine News Corporate News Latest News #Merck #MRK $MRK CHMP Keytruda MSD NSCLC NYSE:MRK Source Type: news
More News: Cancer | Cancer & Oncology | Chemotherapy | European Medicines Agency (EMA) | Lung Cancer | Merck | Non-Small Cell Lung Cancer | Pharmaceuticals