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
-
Merck’s Investigational Insulin Glargine, MK-1293, Met Primary Endpoint in Two Phase 3 Studies, Showing Non-Inferiority to Lantus®
-
Merck and Pfizer Announce Two Pivotal Phase 3 Studies for Ertugliflozin, an Investigational SGLT-2 Inhibitor, Met Primary Endpoints, Showing Significant A1C Reductions in Patients with Type 2 Diabetes
-
Merck to Acquire Afferent Pharmaceuticals
-
Merck (MRK) Enters Agreement to Acquire Afferent Pharma in ~$1.25B Deal
-
Merck to Acquire Afferent Pharmaceuticals
-
KEYTRUDA® (pembrolizumab) Shows Overall Response Rates of 73 to 83 Percent, with Complete Response Rates of 27 to 30 Percent, in Heavily Pre-treated Patients with cHL, in Update to Study KN-087
-
Updated Findings from KEYNOTE-012 for KEYTRUDA® (pembrolizumab) Show Continued Benefit in Response Rates and Duration of Response Lasting Up to 30 Months in Patients with Previously Treated Recurrent
-
Merck (MRK) Announces Presentation of New KEYTRUDA Data in NSCLC
-
New Data from Phase 2 Study Evaluating KEYTRUDA® (pembrolizumab) for the Treatment of Cancers Deficient in DNA Mismatch Repair Show Durable Responses Across a Range of Cancers
-
New Data for KEYTRUDA® (pembrolizumab) in Combination with Talimogene Laherparepvec, Dabrafenib Plus Trametinib, or Low-Dose Ipilimumab in Advanced Melanoma Presented at 2016 ASCO Annual Meeting
-
New KEYTRUDA® (pembrolizumab) Data from KEYNOTE-010 and KEYNOTE-001 in Advanced Non-Small Cell Lung Cancer, Including Survival Data, To Be Presented at 2016 ASCO Annual Meeting
-
New Data Evaluating KEYTRUDA® (pembrolizumab) in Combination with Chemotherapy for First-Line Treatment of Non-Small Cell Lung Cancer Demonstrate Response Rates Ranging from 48 to 71 Percent
-
Merck to Hold Investor Briefing at 2016 ASCO Annual Meeting
-
Merck (MRK) Announces Positive CHMP Opinion for ZEPATIER
-
Merck Receives Positive CHMP Opinion for ZEPATIER™ (elbasvir and grazoprevir) in the European Union
-
Merck Announces Third-Quarter 2016 Dividend
-
Merck to Present at the UBS Global Healthcare Conference
-
Merck (MRK) Plans KEYTRUDA, KEYNOTE-006 and KEYNOTE-001 Presentations at ASCO 2016
-
New KEYTRUDA® (pembrolizumab) Data from KEYNOTE-006 and KEYNOTE-001 in Advanced Melanoma, Including Updated Survival Data, To Be Presented at 2016 ASCO Annual Meeting
-
Merck (MRK) Will Present New KEYTRUDA Data in Head and Neck Cancer, NSCLC
-
New KEYTRUDA® (pembrolizumab) Data at 2016 ASCO Annual Meeting Includes Three-Year Overall Survival Data in Melanoma and Updated Overall Survival Data in Non-Small Cell Lung Cancer As Well As Updated
-
Merck (MRK) Will Present JANUVIA, Diabetes Pipeline, Other Data at 76th Scientific Sessions of the ADA
-
Merck to Present Phase 3 Data on Investigational Medicines Ertugliflozin and MK-1293 at the 76th Scientific Sessions of the American Diabetes Association
-
Merck Announces First-Quarter 2016 Financial Results
-
Merck to Present at the Deutsche Bank 41st Annual Health Care Conference
-
Christina Applegate and Merck Urge Insomnia Sufferers to Learn "Why They're So Awake"
-
Merck, the American Diabetes Association and America's Diabetes Challenge Celebrity Voices Unite to Take on National Health Epidemic
-
Journal of the American Medical Association Publishes Phase III Data from Allergic Asthma Trial with ALK's House Dust Mite SLIT-tablet, ACARIZAX®
-
Merck (MRK) Animal Health Enters Agreement to Acquire Whisper Veterinary Stethoscope System
-
Merck Animal Health to Acquire Worldwide Rights to Whisper® Veterinary Stethoscope System
-
Merck (MRK) Comments on Blueprint PD-L1 Assay Comparison Project; Encouraged by Findings
-
Merck Statement on Blueprint Project Findings Presented at the American Association for Cancer Research 2016 Annual Meeting
-
Merck (MRK) Receives FDA Breakthrough Therapy Designation for KEYTRUDA in cHL
-
Merck Receives Breakthrough Therapy Designation from U.S. Food and Drug Administration for KEYTRUDA® (pembrolizumab) in Classical Hodgkin Lymphoma (cHL)
-
Merck (MRK) Preents Data from Two ZEPATIER Phase 3s; High SVR Demonstrated
-
Merck Announces Results From Phase 3 Studies of ZEPATIER™ (Elbasvir and Grazoprevir) in Chronic Hepatitis C Patient Populations at The International Liver Congress™
-
Merck (MRK) Announces Strong Data from C-EDGE Head-to-Head Study
-
Merck’s ZEPATIER™ (Elbasvir and Grazoprevir) Showed Superiority on Efficacy and Safety Endpoints Compared to Sofosbuvir Plus Peginterferon and Ribavirin Treatment Regimen in Phase 3 Trial
-
Merck (MRK) Announces FDA Acceptance of KEYTRUDA sBLA; Priority Review Granted
-
FDA Accepts Supplemental Biologics License Application (sBLA) for KEYTRUDA® (pembrolizumab) in Recurrent or Metastatic Head and Neck Cancer, and Grants Priority Review
-
Merck to Hold First-Quarter 2016 Sales and Earnings Conference Call on May 5
-
Merck Highlights Ongoing Commitment to Fighting Infectious Diseases with More Than 30 Data Presentations at ECCMID 2016
-
Merck (MRK) Will Present New KEYTRUDA Data at AACR Annual Meeting
-
Merck to Present New Data for KEYTRUDA® (pembrolizumab) at the American Association for Cancer Research 2016 Annual Meeting
-
Pfizer (PFE), Merck (MRK) Treat First Patient in Avelumab Phase 3
-
Advaxis (ADXS), Merck (MRK) Complete First Two Dose Escalations in KEYNOTE-046 Trial
-
Advaxis Combination Trial with Merck Completes First Two Dose-Escalation Cohorts
-
Merck Receives 2016 ENERGY STAR Sustained Excellence Award From U.S. Environmental Protection Agency
-
Merck to Present New Findings from Chronic Hepatitis C Clinical Development Programs at The International Liver CongressTM 2016
-
Merck Applauds the U.S. Department of Veterans Affairs (VA) for Broadening Treatment Access for Veterans with Chronic Hepatitis C Infection

