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Merck to Hold Second-Quarter 2018 Sales and Earnings Conference Call on July 27
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LYNPARZA® (olaparib) Significantly Delays Disease Progression in Phase 3 First-Line SOLO-1 Trial for Ovarian Cancer
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Merck (MRK) Says FDA Accepted sBLA for its KEYTRUDA as Adjuvant Therapy in Advanced Melanoma
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FDA Accepts Supplemental Biologics License Application for Merck’s KEYTRUDA® (pembrolizumab) as Adjuvant Therapy in Advanced Melanoma
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Merck (MRK) Announces New Data from Comparative Trials with Sitagliptin (CompoSIT) Clinical Trial Program with JANUVIA (sitagliptin)
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Merck Presents New Data from the Comparative Trials with Sitagliptin (CompoSIT) Clinical Trial Program with JANUVIA® (sitagliptin)
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Merck (MRK) Announces FDA Approval of its KEYTRUDA for Treatment of Refractory or Relapsed PMBCL
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Treatment of Refractory or Relapsed Primary Mediastinal Large B-Cell Lymphoma (PMBCL)
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Merck (MRK) Says FDA Granted Priority Review to its sBLA for GARDASIL9 in Women and Men Ages 27 to 45 for Prevention of Certain HPV-Related Cancers and Diseases
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FDA Grants Priority Review to Merck’s Supplemental Biologics License Application (sBLA) for GARDASIL®9 in Women and Men Ages 27 to 45 for the Prevention of Certain HPV-Related Cancers and Diseases
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Merck (MRK) Announces FDA Approval of its KEYTRUDA for Previously Treated Patients with Recurrent or Metastatic Cervical Cancer
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Previously Treated Patients with Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS Greater Than or Equal to 1)
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AstraZeneca (AZN), Merck (MRK) Report LYNPARZA in Combination with Abiraterone Delayed Disease Progression in mCRPC
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LYNPARZA® (olaparib) in Combination with Abiraterone Delayed Disease Progression in Metastatic Castration-Resistant Prostate Cancer
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Two-Year Update of Pivotal JAVELIN Merkel 200 Trial Shows Continued Durable Responses with BAVENCIO® (avelumab)
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Merck (MRK) Says KEYTRUDA Showed Promising Anti-Tumor Activity in Patients with Advanced SCLC in Phase 2 KEYNOTE-158 Study
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Merck’s KEYTRUDA® (pembrolizumab) Showed Promising Anti-Tumor Activity in Patients with Advanced Small Cell Lung Cancer (SCLC) in Phase 2 KEYNOTE-158 Study
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Merck (MRK) Highlights Long-Term Survival Benefit in KEYTRUDA® (pembrolizumab)
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Merck’s KEYTRUDA® (pembrolizumab) Demonstrated Long-Term Survival Benefit Based on Four and Five Years of Follow-Up from Two Pivotal Studies in Advanced Melanoma
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Merck (MRK) & Eisai Highlights New Data and Analyses of LENVIMA (lenvatinib) in Combination with Anti-PD-1 Therapy, KEYTRUDA (pembrolizumab)
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Merck's (MRK) KEYTRUDA Plus Chemo Significantly Improved Overall Survival in First-Line Treatment of Metastatic Squamous NSCLC
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Eisai and Merck Announce Data at 2018 ASCO Annual Meeting from Investigational Studies of LENVIMA® (lenvatinib) and KEYTRUDA® (pembrolizumab) Combination Therapy in Four Different Tumor Types
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Merck’s KEYTRUDA® (pembrolizumab) Showed Overall Response Rate of Nearly 40 Percent as First-Line Therapy in Patients with Advanced Clear Cell Renal Cell Carcinoma (RCC) in Phase 2 KEYNOTE-427 Stud
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Merck’s KEYTRUDA® (pembrolizumab) Plus Chemotherapy Significantly Improved Overall Survival in First-Line Treatment of Metastatic Squamous Non-Small Cell Lung Cancer in Phase 3 KEYNOTE-407 Study
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KEYTRUDA® (pembrolizumab) Monotherapy Significantly Improved Overall Survival in KEYNOTE-042 Study as First-Line Treatment for Locally Advanced or Metastatic NSCLC Patients Whose Tumors Expressed PD-
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Advaxis (ADXS) Announced Prelim. Data from Ongoing Metastatic, Castration Resistant Prostate Cancer (mCRPC) Phase 1/2 KEYNOTE-046 Study, Conducted in Conjunction with Merck (MRK) Evaluating ADXS-PSA
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Merck and Premier Inc. Collaborating to Help Reduce Clostridium difficile (C. diff) Infection
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Eisai And Merck Provide Update on Supplemental New Drug Application (sNDA) for Lenvatinib in First-Line Unresectable Hepatocellular Carcinoma
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Foundation Medicine (FMI) Reports Immuno-Oncology Companion Diagnostics Collaboration with Merck (MRK)
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Merck's (MRK) KEYTRUDA Significantly Improved OS and PFS as First-Line Treatment for NSCLC in Pivotal Phase 3 KEYNOTE-407 Trial
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Merck’s KEYTRUDA® (pembrolizumab) Significantly Improved Overall Survival and Progression-Free Survival as First-Line Treatment for Squamous Non-Small Cell Lung Cancer (NSCLC) in Pivotal Phase 3 KE
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Merck Announces Third-Quarter 2018 Dividend
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New Data from Merck’s Leading Immuno-Oncology Clinical Development Program in Over 25 Tumor Types to Be Presented at 2018 ASCO Annual Meeting
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AstraZeneca (AZN), Merck (MRK) LYNPARZA Tablets Receive EU Approval for Treatment of Platinum-Sensitive Relapsed Ovarian Cancer
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LYNPARZA® (olaparib) Tablets Receive EU Approval for the Treatment of Platinum-Sensitive Relapsed Ovarian Cancer
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Veeva Announces Merck’s Expanded Use of Veeva CRM for Latin America and Asia Pacific
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Moderna and Merck (MRK) Expand mRNA Cancer Vaccines Pact
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Moderna and Merck Expand mRNA Cancer Vaccines Collaboration
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Merck (MRK) KEYNOTE-407 Trial Met Pre-specified Secondary Endpoint
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Merck Provides Update on KEYNOTE-407 Trial
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Merck Announces First-Quarter 2018 Financial Results
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Merck (MRK) Announces FDA Granted Priority Review to its sBLA for KEYTRUDA in Combination with Pemetrexed and Platinum Chemotherapy as First-Line Treatment of Metastatic Nonsquamous NSCLC
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FDA Grants Priority Review to Merck’s sBLA for KEYTRUDA® (pembrolizumab) in Combination with Pemetrexed (ALIMTA®) and Platinum Chemotherapy Based on Results from Phase 3 KEYNOTE-189 Trial as Firs
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Merck (MRK) Reports EMA Validation of Type II Variation for KEYTRUDA (pembrolizumab) in Combination with Pemetrexed (ALIMTA) and Platinum Chemotherapy
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European Medicines Agency Validates Type II Variation for Merck’s KEYTRUDA® (pembrolizumab) in Combination with Pemetrexed (ALIMTA®) and Platinum Chemotherapy as First-Line Therapy in Metastatic N
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Merck (MRK) Says It's Beginning Two Phase 3 Studies of PCV-15 (V114), Its Investigational Pneumococcal Disease Vaccine
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Merck Announces First Phase Three Studies for PCV-15 (V114) Its Investigational Pneumococcal Disease Vaccine
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Merck (MRK) Announces Results from KEYNOTE-189, a Pivotal Phase 3 Trial Evaluating KEYTRUDA (anti-PD-1 therapy) in Combination with Pemetrexed (ALIMTA) and Cisplatin
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Merck’s KEYTRUDA® (pembrolizumab) Plus Pemetrexed (ALIMTA®) and Platinum Chemotherapy Reduced the Risk of Death by Half Compared with Chemotherapy Alone as First-Line Treatment for Advanced Nonsqu
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AstraZeneca (AZN) & Merck (MRK) Report Overall Survival Data for LYNPARZA (olaparib) in gBRCA-Mutated HER2-Negative Metastatic Breast Cancer

