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-- October 31, 2024 --

Merck Announces Third-Quarter 2024 Financial Results Business Wire 6:30 AM

-- October 28, 2024 --

Merck and Moderna Initiate Phase 3 Trial Evaluating Adjuvant V940 (mRNA-4157) in Combination with KEYTRUDA (pembrolizumab) After Neoadjuvant KEYTRUDA and Chemotherapy in Patients With Certain Types of Non-Small Cell Lung Cancer (NSCLC) Business Wire 6:45 AM

-- October 24, 2024 --

Merck's KEYTRUDA (pembrolizumab) Receives 30th Approval From European Commission With Two New Indications in Gynecologic Cancers Business Wire 6:45 AM

-- October 23, 2024 --

CDC'S ACIP Recommends Merck's CAPVAXIVE (Pneumococcal 21-valent Conjugate Vaccine) for Pneumococcal Vaccination in Adults 50 Years of Age and Older Business Wire 7:58 PM

-- October 19, 2024 --

Gilead and Merck Announce Phase 2 Data Showing a Treatment Switch to an Investigational Oral Once-Weekly Combination Regimen of Islatravir and Lenacapavir Maintained Viral Suppression in Adults at Week 48 Business Wire 5:09 PM

-- October 17, 2024 --

Merck's Clesrovimab (MK-1654), an Investigational Respiratory Syncytial Virus (RSV) Preventative Monoclonal Antibody, Significantly Reduced Incidence of RSV Disease and Hospitalization in Healthy Preterm and Full-term Infants Business Wire 6:00 PM

-- October 16, 2024 --

Merck's CAPVAXIVE (Pneumococcal 21-valent Conjugate Vaccine) Demonstrates Positive Immune Responses in Adults with Increased Risk for Pneumococcal Disease Business Wire 6:45 AM

-- October 14, 2024 --

Exelixis and Merck Sign Clinical Development Collaboration to Evaluate Investigational Zanzalintinib in Combination with KEYTRUDA (pembrolizumab) in Head and Neck Cancer and in Combination with WELIREG (belzutifan) in Renal Cell Carcinoma Business Wire 8:00 AM

-- October 9, 2024 --

New Data to be Presented at IDWeek 2024 Reinforce Merck's Broad and Diverse Vaccines and Infectious Disease Pipeline and Portfolio Business Wire 6:45 AM

-- October 8, 2024 --

Merck's KEYTRUDA (pembrolizumab) Met Primary Endpoint of Event-Free Survival (EFS) as Perioperative Treatment Regimen in Patients With Resected, Locally Advanced Head and Neck Squamous Cell Carcinoma Business Wire 6:45 AM

-- October 1, 2024 --

Merck Completes Acquisition of Investigational B-Cell Depletion Therapy, CN201, from Curon Biopharmaceutical Business Wire 6:45 AM
Merck to Hold Third-Quarter 2024 Sales and Earnings Conference Call Oct. 31 Business Wire 6:30 AM

-- September 26, 2024 --

Merck to Present New Long-Term Data for Tulisokibart (MK-7240), an Investigational Anti-TL1A Monoclonal Antibody, in Inflammatory Bowel Disease at UEG Week 2024 Business Wire 6:45 AM

-- September 25, 2024 --

Merck Provides Update on Phase 3 KEYFORM-007 Trial Evaluating Investigational Fixed-Dose Combination of Favezelimab and Pembrolizumab for Patients With Previously Treated PD-L1 Positive Microsatellite Stable Metastatic Colorectal Cancer Business Wire 6:45 AM
Merck's KEYTRUDA (pembrolizumab) Receives New Approvals in Japan for Certain Patients With Non-Small Cell Lung Carcinoma (NSCLC) and Radically Unresectable Urothelial Carcinoma Business Wire 6:30 AM

-- September 24, 2024 --

Merck Animal Health Announces Expansion of NOBIVAC NXT Platform with the First and Only RNA-Particle Technology Vaccine for Feline Leukemia Virus Business Wire 8:06 AM

-- September 20, 2024 --

How Critical Demand for Metastatic Breast Cancer Therapies is Producing a Multi-Billion Dollar Opportunity for Biotechs Globe Newswire 9:00 AM
Merck Receives Positive EU CHMP Opinions for KEYTRUDA (pembrolizumab) Regimens as Treatment for Patients With Two Types of Gynecologic Cancers Business Wire 7:30 AM

-- September 18, 2024 --

FDA Approves Merck's KEYTRUDA (pembrolizumab) Plus Pemetrexed and Platinum Chemotherapy as First-Line Treatment for Adult Patients With Unresectable Advanced or Metastatic Malignant Pleural Mesothelioma (MPM) Business Wire 6:45 AM

-- September 17, 2024 --

Patritumab Deruxtecan Demonstrated Statistically Significant Improvement in Progression-Free Survival Versus Doublet Chemotherapy in Patients with Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer in HERTHENA-Lung02 Phase 3 Trial Business Wire 6:00 AM

-- September 16, 2024 --

PESG Releases Report on Nuvectis Pharma: With Summit Therapeutics Threatening to Dethrone Merck's Keytruda, Nuvectis' NXP900 is One to Watch Business Wire 7:15 AM
BeyondSpring Presents Efficacy/Safety Results from a Phase 2 Study of Pembrolizumab plus Plinabulin/Docetaxel in Metastatic NSCLC after Progressing on First-Line Immune Checkpoint Inhibitors at ESMO Congress 2024 Globe Newswire 7:00 AM

-- September 15, 2024 --

KEYTRUDA (pembrolizumab) Plus Chemotherapy Before Surgery and Continued as Single Agent After Surgery Reduced Risk of Death by More Than One-Third (34%) Versus Neoadjuvant Chemotherapy in High-Risk Early-Stage Triple-Negative Breast Cancer (TNBC) Business Wire 10:30 AM
Ten-Year Data for Merck's KEYTRUDA (pembrolizumab) Demonstrates Sustained Overall Survival Benefit Versus Ipilimumab in Advanced Melanoma Business Wire 8:45 AM

-- September 14, 2024 --

KEYTRUDA (pembrolizumab) Plus LENVIMA (lenvatinib) in Combination With Transarterial Chemoembolization Significantly Improved Progression-Free Survival Compared to TACE Alone in Patients With Unresectable, Non-Metastatic Hepatocellular Carcinoma Business Wire 10:35 AM
Merck's KEYTRUDA (pembrolizumab) Plus Chemoradiotherapy (CRT) Reduced Risk of Death by 33% Versus CRT Alone in Patients With Newly Diagnosed High-Risk Locally Advanced Cervical Cancer Business Wire 10:30 AM
KEYTRUDA (pembrolizumab) Plus Trastuzumab and Chemotherapy Significantly Improved Overall Survival (OS) Versus Trastuzumab and Chemotherapy Alone in First-Line Treatment of Patients With HER2-Positive Advanced Gastric or GEJ Adenocarcinoma Business Wire 3:15 AM

-- September 11, 2024 --

Merck to Participate in the Bank of America 2024 Global Healthcare Conference Business Wire 6:45 AM
Merck Announces Positive Top-line Results from Phase 3 Trial Evaluating Efficacy and Safety of GARDASIL9 in Japanese Males Business Wire 6:30 AM

-- September 10, 2024 --

Junior Biotech Utilizes AI To Shorten Drug Discovery Timelines, Ultimately Saving Lives Yolowire 6:58 PM

-- September 7, 2024 --

Ifinatamab Deruxtecan Continues to Demonstrate Promising Objective Response Rates in Patients with Extensive-Stage Small Cell Lung Cancer in IDeate-Lung01 Phase 2 Trial Business Wire 11:30 AM

-- September 4, 2024 --

Merck to Present Survival Data and New Research on 10 Investigational or Approved Medicines at ESMO Congress 2024 Business Wire 6:45 AM
Merck and EyeBio Announce Initiation of Phase 2b/3 Clinical Trial for Restoret for the Treatment of Diabetic Macular Edema Business Wire 6:40 AM

-- September 3, 2024 --

European Commission Approves Merck's KEYTRUDA (pembrolizumab) Plus Padcev (enfortumab vedotin-ejfv) as First-Line Treatment of Unresectable or Metastatic Urothelial Carcinoma in Adults Business Wire 6:45 AM

-- August 29, 2024 --

Merck to Participate in the Morgan Stanley 22nd Annual Global Healthcare Conference Business Wire 6:45 AM
Merck Provides Update on Phase 3 KEYNOTE-867 and KEYNOTE-630 Trials Business Wire 6:30 AM

-- August 27, 2024 --

Merck Announces Phase 3 Trial Initiation for Bomedemstat, an Investigational Candidate for the Treatment of Certain Patients With Essential Thrombocythemia Business Wire 6:45 AM

-- August 26, 2024 --

Merck Receives European Commission Approval for WINREVAIR (sotatercept) in Combination With Other Pulmonary Arterial Hypertension (PAH) Therapies, for the Treatment of PAH in Adult Patients With Functional Class II-III Business Wire 6:45 AM

-- August 9, 2024 --

Merck to Acquire Investigational B-Cell Depletion Therapy, CN201, from Curon Biopharmaceutical Business Wire 6:45 AM

-- August 8, 2024 --

Merck Provides Update on Phase 3 KeyVibe-008 Trial Evaluating an Investigational Fixed-Dose Combination of Vibostolimab and Pembrolizumab in Patients With Extensive-Stage Small Cell Lung Cancer Business Wire 6:45 AM

-- August 6, 2024 --

Ligand Reports Second Quarter 2024 Financial Results Business Wire 4:01 PM
Alzheimer's Disease Diagnostics & Therapeutics Market Driven by Use of Biomarkers and Advancing R&D Activities Globe Newswire 9:00 AM
Daiichi Sankyo and Merck Enter into Global Development and Commercialization Agreement for MK-6070 Business Wire 6:45 AM

-- August 1, 2024 --

IDeate-Lung02 Phase 3 Trial of Ifinatamab Deruxtecan Initiated in Patients with Relapsed Small Cell Lung Cancer Business Wire 8:00 AM

-- July 30, 2024 --

Merck Announces Second-Quarter 2024 Financial Results Business Wire 6:30 AM

-- July 26, 2024 --

Merck Receives Positive EU CHMP Opinion for KEYTRUDA (pembrolizumab) Plus Padcev (enfortumab vedotin-ejfv) as First-Line Treatment for Patients With Unresectable or Metastatic Urothelial Carcinoma Business Wire 6:50 AM

-- July 23, 2024 --

Merck Announces Fourth-Quarter 2024 Dividend Business Wire 12:52 PM
Merck Announces Topline Results from Phase 2b/3 Trial of Clesrovimab (MK-1654), an Investigational Respiratory Syncytial Virus Preventative Monoclonal Antibody for Infants Business Wire 6:45 AM

-- July 16, 2024 --

Merck to Share New Research and Host Community-Focused Symposia at AIDS 2024 Business Wire 6:45 AM
Jeito Capital consolidates its support in CatalYm with a renewed participation in a $150 million financing Globe Newswire 5:10 AM

-- July 12, 2024 --

Merck Completes Acquisition of EyeBio Business Wire 6:45 AM

-- July 9, 2024 --

Merck Animal Health Completes Acquisition of Elanco's Aqua Business Business Wire 8:30 AM
Elanco Completes Sale of Aqua Business PRNewswire 8:28 AM

-- July 1, 2024 --

Merck and Orion Announce Mutual Exercise of Option Providing Merck Global Exclusive Rights to Opevesostat, an Investigational CYP11A1 Inhibitor, for the Treatment of Metastatic Castration-Resistant Prostate Cancer Business Wire 8:15 AM
Merck to Hold Second-Quarter 2024 Sales and Earnings Conference Call July 30 Business Wire 6:45 AM

-- June 28, 2024 --

Merck Receives Positive EU CHMP Opinion for WINREVAIR (sotatercept) in Pulmonary Arterial Hypertension (PAH) Business Wire 6:53 AM

-- June 27, 2024 --

CDC'S ACIP Unanimously Recommends Merck's CAPVAXIVE (Pneumococcal 21-valent Conjugate Vaccine) for Pneumococcal Vaccination in Appropriate Adults Business Wire 8:18 PM

-- June 26, 2024 --

Patritumab Deruxtecan BLA Submission Receives Complete Response Letter from FDA Due to Inspection Findings at Third-Party Manufacturer Business Wire 7:45 PM

-- June 25, 2024 --

USDA Approves Merck Animal Health's NOBIVAC NXT Canine Flu H3N2 The First and Only RNA-Particle Technology Vaccine for Canine Influenza Business Wire 4:05 PM

-- June 20, 2024 --

Pancreatic Cancer Market Is Projecting to Expand As NCI-Funded Research Expects to Empower Market Growth Globe Newswire 10:00 AM

-- June 17, 2024 --

U.S. FDA Approves CAPVAXIVE (Pneumococcal 21-valent Conjugate Vaccine) for Prevention of Invasive Pneumococcal Disease and Pneumococcal Pneumonia in Adults Business Wire 5:29 PM
FDA Approves Merck's KEYTRUDA (pembrolizumab) Plus Carboplatin and Paclitaxel as Treatment for Adult Patients With Primary Advanced or Recurrent Endometrial Carcinoma Business Wire 5:15 PM

-- June 5, 2024 --

Merck to Participate in the Goldman Sachs 45th Annual Global Healthcare Conference Business Wire 6:45 AM

-- June 3, 2024 --

Moderna & Merck Announce 3-Year Data For mRNA-4157 (V940) in Combination With KEYTRUDA(R) (pembrolizumab) Demonstrated Sustained Improvement in Recurrence-Free Survival & Distant Metastasis-Free Survival Versus KEYTRUDA in Patients With High-Risk Stage III/IV Melanoma Following Complete Resection ACCESSWIRE 8:01 AM