Merck's 2Q results next week will reveal the state of Keytruda demand in the USProactive Investors • 07/27/23
Merck Announces V116, an Investigational, 21-valent Pneumococcal Conjugate Vaccine Specifically Designed for Adults, Met Key Immunogenicity and Safety Endpoints in Two Phase 3 TrialsBusiness Wire • 07/27/23
Merck and Moderna launch late-stage trial of V940 with Keytruda as treatment for high-risk melanomaMarket Watch • 07/26/23
Merck and Moderna Initiate Phase 3 Study Evaluating V940 (mRNA-4157) in Combination with KEYTRUDA® (pembrolizumab) for Adjuvant Treatment of Patients with Resected High-Risk (Stage IIB-IV) MelanomaBusiness Wire • 07/26/23
Merck Receives Positive EU CHMP Opinion for KEYTRUDA® (pembrolizumab) Plus Trastuzumab and Chemotherapy as First-Line Treatment for HER2-Positive Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma Expressing PD-L1 (CPS ≥1)Business Wire • 07/21/23
Merck Announces Phase 3 KEYNOTE-A18 Trial Met Primary Endpoint of Progression-Free Survival (PFS) in Patients With Newly Diagnosed High-Risk Locally Advanced Cervical CancerBusiness Wire • 07/19/23
First Patient Dosed in STARSTRUCK Study of TLX250 Targeted Radiation Therapy in Combination with Merck Investigational DNA-PK Inhibitor, PeposertibPRNewsWire • 07/18/23
Johnson & Johnson joins Merck, others, in fighting Medicare drug-price programMarket Watch • 07/18/23
Merck and AbbVie Are Facing Big Patent Cliffs, But Here's Why Both Are Still BuysThe Motley Fool • 07/03/23
Week In Review: CMBG Out-Licenses Two CAR-T Candidates To Janssen For $245 Million UpfrontSeeking Alpha • 07/02/23