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Aug 25, 2023 06:30AM Merck Initiates Phase 3 Clinical Program for Oral PCSK9 Inhibitor Candidate MK-0616
Aug 25, 2023 06:24AM Merck (MRK) and Eisai Provide Update on Phase 3 LEAP-010 Trial of KEYTRUDA pus LENVIMA
Aug 25, 2023 06:15AM Merck and Eisai Provide Update on Phase 3 LEAP-010 Trial Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Patients With Certain Types of Recurrent or Metastatic Head and Neck Squam
Aug 24, 2023 06:45AM Merck (MRK) Reports LYNPARZA Plus Abiraterone and Prednisone or Prednisolone Approved in Japan for the Treatment of BRCA-Mutated Metastatic Castration-Resistant Prostate Cancer
Aug 24, 2023 06:45AM LYNPARZA® (olaparib) Plus Abiraterone and Prednisone or Prednisolone Approved in Japan for the Treatment of BRCA-Mutated Metastatic Castration-Resistant Prostate Cancer
Aug 18, 2023 06:46AM Merck (MRK) Reports WELIREG Phase 3 LITESPARK-005 Trial Met Primary Endpoint
Aug 18, 2023 06:45AM Merck Announces WELIREG® (belzutifan) Phase 3 LITESPARK-005 Trial Met Primary Endpoint of Progression-Free Survival in Certain Previously Treated Patients With Advanced Renal Cell Carcinoma
Aug 8, 2023 04:01PM Ligand Reports Second Quarter 2023 Financial Results
Aug 7, 2023 08:30AM Anixa Biosciences Announces Opening of Enrollment for Keytruda® Arm in Ongoing Breast Cancer Vaccine Clinical Trial
Aug 3, 2023 06:45AM Merck (MRK) Announces FDA Approval of ERVEBO for Use in Children 12 Months of Age and Older
Aug 3, 2023 06:45AM U.S. FDA Approves Merck’s ERVEBO® (Ebola Zaire Vaccine, Live) for Use in Children 12 Months of Age and Older
Aug 1, 2023 06:30AM Merck Announces Second-Quarter 2023 Financial Results
Aug 1, 2023 05:57AM Busy earnings day, Meta reportedly prepares AI chatbot - what's moving markets
Jul 28, 2023 06:45AM Merck (MRK) Reports Phase 3 KEYNOTE-756 Trial Met Primary Endpoint
Jul 28, 2023 06:45AM Merck Announces Phase 3 KEYNOTE-756 Trial Met Primary Endpoint of Pathological Complete Response (pCR) Rate in Patients With High-Risk, Early-Stage ER+/HER2- Breast Cancer
Jul 27, 2023 06:45AM Merck (MRK) Announces V116 Met Key Immunogenicity and Safety Endpoints in Two Phase 3 Trials
Jul 27, 2023 06:45AM Merck Announces V116, an Investigational, 21-valent Pneumococcal Conjugate Vaccine Specifically Designed for Adults, Met Key Immunogenicity and Safety Endpoints in Two Phase 3 Trials
Jul 26, 2023 06:45AM Merck (MRK) and Moderna (MRNA) Initiate Phase 3 Study Evaluating V940 in Combination with KEYTRUDA
Jul 26, 2023 06:45AM 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) Melanoma
Jul 25, 2023 12:58PM Merck Announces Fourth-Quarter 2023 Dividend
Jul 21, 2023 07:52AM Merck (MRK) Receives Positive European Union CHMP Opinion for Gefapixant
Jul 21, 2023 07:52AM Merck (MRK) Receives Positive EU CHMP Opinion for KEYTRUDA Plus Trastuzumab and Chemotherapy as First-Line Treatment for HER2-Positive Advanced Gastric or Gastroesophageal Junction (GEJ) Adenocarcinom
Jul 21, 2023 07:52AM Merck Receives Positive European Union CHMP Opinion for Gefapixant
Jul 21, 2023 07:50AM 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) A
Jul 19, 2023 06:46AM Merck (MRK) Announces Phase 3 KEYNOTE-A18 Trial Met Primary Endpoint of Progression-Free Survival (PFS)
Jul 19, 2023 06:45AM 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 Cancer
Jul 17, 2023 08:45AM Argus adds Adobe (ADBE), Merck (MRK), Tesla (TSLA), Walmart (WMT) to its Focus List
Jul 12, 2023 11:30AM MilliporeSigma Invests $25 Million to Expand Cell Culture Media Production in Kansas
Jul 11, 2023 09:05AM Athinia™ expands partnerships to include Tokyo Electron for real-time collaborative analytics of semiconductor fab equipment performance
Jun 29, 2023 06:45AM Merck to Hold Second-Quarter 2023 Sales and Earnings Conference Call on Aug. 1
Jun 20, 2023 06:47AM Merck (MRK) Provides Update on Phase 3 KEYNOTE-585 Trial
Jun 20, 2023 06:45AM Merck Provides Update on Phase 3 KEYNOTE-585 Trial in Locally Advanced Resectable Gastric and Gastroesophageal Junction (GEJ) Adenocarcinoma
Jun 16, 2023 04:04PM Merck (MRK) Completes Acquisition of Prometheus Biosciences (RXDX)
Jun 16, 2023 04:04PM Merck Completes Acquisition of Prometheus Biosciences, Inc.
Jun 16, 2023 06:45AM Merck (MRK) Reports KEYTRUDA Plus Trastuzumab and Chemotherapy Met Primary Endpoint of Progression-Free Survival as First-Line Treatment in Patients With HER2-Positive Advanced Gastric or Gastroesopha
Jun 16, 2023 06:45AM KEYTRUDA® (pembrolizumab) Plus Trastuzumab and Chemotherapy Met Primary Endpoint of Progression-Free Survival as First-Line Treatment in Patients With HER2-Positive Advanced Gastric or Gastroesophage
Jun 13, 2023 04:05PM U.S. District Court for the District of New Jersey Rules in Favor of Merck in Patent Infringement Lawsuit Related to BRIDION® (sugammadex)
Jun 12, 2023 06:45AM Merck to Present Data for Efinopegdutide (MK-6024), an Investigational GLP-1/Glucagon Receptor Co-agonist, in Patients with Nonalcoholic Fatty Liver Disease (NAFLD) at EASL 2023
Jun 8, 2023 06:46AM Merck (MRK) Announces FDA Acceptance of Application for KEYTRUDA Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer
Jun 8, 2023 06:45AM FDA Accepts Application for Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy as Treatment for Advanced or Unresectable Biliary Tract Cancer
Jun 6, 2023 08:00AM MilliporeSigma Announces Proteologix as Winner of its North American Advance Biotech Grant
Jun 6, 2023 06:51AM Merck (MRK) Announces FDA Approval of New Indication for PREVYMIS for CMV Disease in High-Risk Adult Kidney Transplant Recipients
Jun 6, 2023 06:50AM U.S. FDA Approves New Indication for Merck’s PREVYMIS® (letermovir) for Prevention of Cytomegalovirus (CMV) Disease in High-Risk Adult Kidney Transplant Recipients
Jun 6, 2023 06:45AM Merck to Participate in the Goldman Sachs 44th Annual Global Healthcare Conference
Jun 5, 2023 08:01AM Moderna (MRNA) and Merck (MRK) Announce mRNA-4157 in Combination With KEYTRUDA Demonstrated a Statistically Significant and Clinically Meaningful Improvement in Distant Metastasis-Free Survival in Pat
Jun 3, 2023 09:00AM Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Before Surgery and Continued as a Single Agent After Surgery Reduced the Risk of Event-Free Survival Events by 42% Versus Pre-Operative Chemothe
Jun 3, 2023 08:00AM KEYTRUDA® (pembrolizumab) Plus Chemotherapy Significantly Improved Overall Survival Versus Chemotherapy Alone as First-Line Treatment for Unresectable Advanced Pleural Mesothelioma
Jun 1, 2023 07:03AM AstraZeneca (AZN) and Merck (MRK) Announce LYNPARZA plus abiraterone approved in the US for the treatment of BRCA-mutated metastatic castration-resistant prostate cancer
Jun 1, 2023 06:45AM Merck (MRK) Announces FDA Approval of LYNPARZA Plus Abiraterone and Prednisone or Prednisolone for Treatment of Adult Patients With BRCA-Mutated mCRPC
Jun 1, 2023 06:45AM FDA Approves LYNPARZA® (olaparib) Plus Abiraterone and Prednisone or Prednisolone for Treatment of Adult Patients With BRCA-Mutated Metastatic Castration-Resistant Prostate Cancer (mCRPC)
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