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marketscreener.com
Merck & Co., Inc. Announces KEYLYNK-008 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LYNPARZA® for Patients With Metastatic Squamous Non-Small Cell Lung
Merck & Co., Inc. announced that it will stop the Phase 3 KEYLYNK-008 trial evaluating KEYTRUDA, Merck?s anti-PD-1 therapy, in combination with maintenance LYNPARZA, a PARP inhibitor, for the...
Dec 7, 2023
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Just Published: Adjuvant pembrolizumab after resected stage III melanoma led to a 5-year recurrence-free survival of 55.4%, compared with 38.3% in patients treated with placebo. Read more in NEJM Evidence: https://eviden.cc/3x6Wg6l #ESMO22 | The New England Journal of Medicine
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