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Merck (MRK) stops Phase 3 KEYLYNK-008 KEYTRUDA trial in NSCLC after it did not not demonstrate improvement in overall survival

Merck (MRK) stops Phase 3 KEYLYNK-008 KEYTRUDA trial in NSCLC after it did not not demonstrate improvement in overall survival
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Merck Announces Findings from Phase 2 KeyVibe-002 Trial Evaluating an Investigational Coformulation of Vibostolimab and Pembrolizumab in Previously Treated Patients with Metastatic Non-Small Cell Lung Cancer (NSCLC)

Merck Announces KEYLYNK-008 Trial Evaluating KEYTRUDA (pembrolizumab) Plus LYNPARZA (olaparib) for Patients With Metastatic Squamous Non-Small Cell Lung Cancer to Stop for Futility

07.12.2023 - Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today 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 .

Data Support Immunogenicity of 21-Valent Pneumococcal Conjugate Vaccine

Merck’s investigational 21-valent pneumococcal conjugate vaccine, V116, achieved positive immune responses in pneumococcal vaccine-naïve adults.

Merck (MRK) STRIDE-3 Trial of V116 Vaccine Demonstrated Superior Immunogenicity vs PCV20 in Older Adults

Merck (MRK) STRIDE-3 Trial of V116 Vaccine Demonstrated Superior Immunogenicity vs PCV20 in Older Adults
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