http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
MilliporeSigma Joins TRANSVAC2 Program to Advance Vaccine Development and Manufacturing
-
New Research from Merck’s Broad Oncology Clinical Development Program to be Presented at 2019 ASCO Annual Meeting
-
FDA Approves BAVENCIO® (avelumab) Plus INLYTA® (axitinib) Combination for Patients with Advanced Renal Cell Carcinoma
-
Katie Couric Joins Merck and Cancer Advocates to Support Patients and Caregivers Through the Expansion of Your Cancer Game Plan (YCGP)
-
Merck (MRK) Reports Results from Phase 2 Trial of Investigational 15-valent Pneumococcal Conjugate Vaccine (V114) in Infants
-
Merck Announces Results from Phase 2 Trial of Investigational 15-valent Pneumococcal Conjugate Vaccine (V114) in Infants
-
Merck's (MRK) BELSOMRA C-IV Meets Primary Efficacy Endpoint in Phase 3 Trial for Treatment of Insomnia in People with Mild-to-Moderate Alzheimer’s Disease Dementia
-
Merck’s BELSOMRA® (suvorexant) C-IV Meets Primary Efficacy Endpoint in Phase 3 Trial for the Treatment of Insomnia in People with Mild-to-Moderate Alzheimer’s Disease Dementia
-
Merck Announces First-Quarter 2019 Financial Results
-
Merck (MRK) Announces LYNPARZA Receives Positive EU CHMP Opinion for First-Line Maintenance Treatment in BRCA-Mutated Advanced Ovarian Cance
-
LYNPARZA® (olaparib) Receives Positive EU CHMP Opinion for First-Line Maintenance Treatment in BRCA-Mutated Advanced Ovarian Cancer
-
Merck (MRK) Phase 3 KEYNOTE-062 Trial Evaluating KEYTRUDA Met Primary Endpoint, Was not Found to be Superior for OS
-
Merck Provides Update on Phase 3 KEYNOTE-062 Trial Evaluating KEYTRUDA® (pembrolizumab) as Monotherapy and in Combination with Chemotherapy for First-Line Treatment of Patients with Advanced Gastric
-
Merck and Viola Davis to Debut A Touch of Sugar During Tribeca Film Festival®
-
Merck (MRK) Reports FDA Approval of KEYTRUDA (pembrolizumab) in Combination With Inlyta®= (axitinib)
-
FDA Approves Merck’s KEYTRUDA® (pembrolizumab) in Combination With Inlyta® (axitinib) as First-Line Treatment for Patients With Advanced Renal Cell Carcinoma (RCC)
-
Results of Phase 3 Trial Evaluating Merck’s ZERBAXA® (ceftolozane and tazobactam) versus Meropenem for Treatment of Adult Patients with Ventilated Nosocomial Pneumonia (VNP) to be Presented at ECCM
-
Merck (MRK) Announces FDA Approval of Expanded Monotherapy Label for its KEYTRUDA
-
FDA Approves Expanded Monotherapy Label for Merck’s KEYTRUDA® (pembrolizumab)
-
AstraZeneca (AZN) and Merck's (MRK) LYNPARZA Approved in EU for Treatment of Germline BRCA-Mutated HER2-Negative Advanced Breast Cancer
-
LYNPARZA® (olaparib) Approved in EU for the Treatment of Germline BRCA-Mutated HER2-Negative Advanced Breast Cancer
-
Myriad Genetics (MYGN), AstraZeneca (AZN) and Merck (MRK) Expand Companion Diagnostic Partnership
-
Merck (MRK) Completes Tender Offer to Acquire Immune Design (IMDZ)
-
Merck Completes Tender Offer to Acquire Immune Design
-
Merck to Hold First-Quarter 2019 Sales and Earnings Conference Call on April 30
-
Merck Completes Acquisition of Antelliq Corporation to Become Leader in Emerging Digital Technology for Livestock and Companion Animals
-
Merck (MRK) Reports Data for KEYTRUDA (pembrolizumab) Across Different Types of Advanced Lung Cancer Presented at AACR 2019
-
Data for Merck’s KEYTRUDA® (pembrolizumab) Across Different Types of Advanced Lung Cancer Presented at AACR Annual Meeting 2019
-
Merck's (MRK) KEYTRUDA Approved in China for First-Line Treatment of Metastatic Nonsquamous NSCLC in Combination with Chemotherapy
-
Merck’s KEYTRUDA® (pembrolizumab) Approved in China for First-Line Treatment of Metastatic Nonsquamous Non-Small Cell Lung Cancer (NSCLC) in Combination with Chemotherapy
-
AstraZeneca (AZN) and Merck (MRK) Announce Selumetinib Granted U.S. Breakthrough Therapy Designation in Neurofibromatosis Type 1
-
Selumetinib Granted U.S. Breakthrough Therapy Designation in Neurofibromatosis Type 1
-
Merck (MRK), NGM Bio Announce Extension of Broad, Multi-Year Strategic Collaboration
-
Merck and NGM Bio Announce Extension of Broad, Multi-Year Strategic Collaboration to 2022
-
MilliporeSigma Opens First M Lab™ Collaboration Center in Europe
-
MilliporeSigma to Collaborate with GenScript to Accelerate Cell and Gene Therapy Industrialization in China
-
Merck (MRK) Says EC Approved its KEYTRUDA in Combination with Chemotherapy for First-Line Treatment of Adults with Metastatic Squamous NSCLC
-
European Commission Approves Merck’s KEYTRUDA® (pembrolizumab) in Combination with Chemotherapy for First-Line Treatment of Adults with Metastatic Squamous Non-Small Cell Lung Cancer (NSCLC)
-
Merck Begins Tender Offer to Acquire Immune Design
-
MilliporeSigma Awarded Canadian CRISPR Nickase Patent for Foundational Genome-Editing Technology
-
Merck (MRK) Announces EMA Adopts Positive Opinion for its KEYTRUDA for Six-Week Dosing Schedule Across All Current Monotherapy Indications
-
European Medicines Agency Adopts Positive Opinion for Merck’s KEYTRUDA® (pembrolizumab) for Six-Week Dosing Schedule Across All Current Monotherapy Indications
-
Merck (MRK) Announces LYNPARZA Received Positive EU CHMP Opinion For Use in Germline BRCA-Mutated HER2-
-
LYNPARZA® (olaparib) Receives Positive EU CHMP Opinion For Use in Germline BRCA-Mutated HER2-Negative Advanced Breast Cancer
-
Merck (MRK), AstraZeneca (AZN) Say LYNPARZA Reduced Risk of Disease Progression or Death as First-Line Maintenance Treatment in gBRCAm
-
LYNPARZA® (olaparib) Reduced the Risk of Disease Progression or Death as First-Line Maintenance Treatment in Germline BRCA-Mutated Metastatic Pancreatic Cancer
-
Merck (MRK) to Acquire Immune Design (IMDZ) for $5.85/Share
-
Merck to Acquire Immune Design
-
Merck (MRK) Says FDA Granted Priority Review to its sBLA for KEYTRUDA Monotherapy for Third-Line Treatment of Patients with Advanced SCLC
-
FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA® (pembrolizumab) Monotherapy for Third-Line Treatment of Patients with Advanced Small Cell Lung Cancer


