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AstraZeneca and Merck’s LYNPARZA® (olaparib) Approved in Japan as First-Line Maintenance Therapy in Patients with BRCA-Mutated Advanced Ovarian Cancer
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Merck (MRK) Announces FDA Approved its KEYTRUDA as Monotherapy for Some Patients with Metastatic SCLC with Disease Progression
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) as Monotherapy for Patients with Metastatic Small Cell Lung Cancer (SCLC) with Disease Progression on or After Platinum-Based Chemotherapy and at Leas
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LYNPARZA® (olaparib) Approved in the EU for Use as First-Line Maintenance Therapy in Patients With BRCA-Mutated Advanced Ovarian Cancer
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IBM (IBM), Merck (MRK), Walmart (WMT), KPMG to Collaborate with FDA on Pharma Product Integrity Protection Using Blockchain
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IBM, KPMG, Merck and Walmart to collaborate as part of FDA's program to evaluate the use of blockchain to protect pharmaceutical product integrity
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Merck (MRK) Announces FDA Approved Two New Indications for KEYTRUDA
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FDA Approves Two New Indications for Merck’s KEYTRUDA® (pembrolizumab)
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Merck (MRK) to Acquire Tilos Therapeutics for up to $773 Million
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Merck to Acquire Tilos Therapeutics
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Merck (MRK) Confirms FDA Approved its ZERBAXA 3g Dose for Treatment of Adults with HABP/VABP
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FDA Approves Merck’s ZERBAXA® (ceftolozane and tazobactam) 3g Dose for the Treatment of Adults with Hospital-Acquired and Ventilator-Associated Bacterial Pneumonia (HABP/VABP)
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Merck's (MRK) LYNPARZA Phase 3 SOLO3 Trial Demonstrated 72% OR Rate in Patients with Platinum-Sensitive Relapsed gBRCAm
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LYNPARZA® (olaparib) Phase 3 SOLO3 Trial Demonstrated a 72% Objective Response Rate in Patients with Platinum-Sensitive Relapsed Germline BRCA-mutated Advanced Ovarian Cancer Compared to 51% of Patie
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Merck (MRK), AstraZeneca (AZN) Report Results from Phase 3 POLO trial evaluating LYNPARZA as First-Line Maintenance Therapy
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LYNPARZA® (olaparib) First-Line Maintenance Therapy Nearly Doubled the Time Without Disease Progression or Death in Phase 3 POLO Trial for Patients with Germline BRCA-Mutated Metastatic Pancreatic Ca
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Five-Year Survival Data for Merck’s KEYTRUDA® (pembrolizumab) in Advanced Non-Small Cell Lung Cancer (NSCLC) from First KEYNOTE Trial at 2019 ASCO Annual Meeting
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Merck's (MRK) KEYTRUDA (pembrolizumab) Demonstrates Improved OS at Final Analysis of Pivotal Phase 3 KEYNOTE-048 Trial
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Merck’s KEYTRUDA® (pembrolizumab) Demonstrates Improved Overall Survival as First-Line Treatment of Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma at Final Analysis of Pivotal Phase
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Merck Announces Third-Quarter 2019 Dividend
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Merck (MRK) to Acquire Peloton Therapeutics for $1.05 Billion Upfront, Plus $1.15 Billion Contingent
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Merck to Acquire Peloton Therapeutics, Bolstering Oncology Pipeline
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Merck (MRK) Phase 3 KEYNOTE-119 Study of KEYTRUDA Monotherapy in Previously-Treated Patients with Metastatic Triple-Negative Breast Cancer Doesn't Meet Primary Endpoint
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Merck Provides Update on Phase 3 KEYNOTE-119 Study of KEYTRUDA® (pembrolizumab) Monotherapy in Previously-Treated Patients with Metastatic Triple-Negative Breast Cancer
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MilliporeSigma Joins TRANSVAC2 Program to Advance Vaccine Development and Manufacturing
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New Research from Merck’s Broad Oncology Clinical Development Program to be Presented at 2019 ASCO Annual Meeting
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FDA Approves BAVENCIO® (avelumab) Plus INLYTA® (axitinib) Combination for Patients with Advanced Renal Cell Carcinoma
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Katie Couric Joins Merck and Cancer Advocates to Support Patients and Caregivers Through the Expansion of Your Cancer Game Plan (YCGP)
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Merck (MRK) Reports Results from Phase 2 Trial of Investigational 15-valent Pneumococcal Conjugate Vaccine (V114) in Infants
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Merck Announces Results from Phase 2 Trial of Investigational 15-valent Pneumococcal Conjugate Vaccine (V114) in Infants
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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
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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
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Merck Announces First-Quarter 2019 Financial Results
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Merck (MRK) Announces LYNPARZA Receives Positive EU CHMP Opinion for First-Line Maintenance Treatment in BRCA-Mutated Advanced Ovarian Cance
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LYNPARZA® (olaparib) Receives Positive EU CHMP Opinion for First-Line Maintenance Treatment in BRCA-Mutated Advanced Ovarian Cancer
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Merck (MRK) Phase 3 KEYNOTE-062 Trial Evaluating KEYTRUDA Met Primary Endpoint, Was not Found to be Superior for OS
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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
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Merck and Viola Davis to Debut A Touch of Sugar During Tribeca Film Festival®
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Merck (MRK) Reports FDA Approval of KEYTRUDA (pembrolizumab) in Combination With Inlyta®= (axitinib)
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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) in Combination With Inlyta® (axitinib) as First-Line Treatment for Patients With Advanced Renal Cell Carcinoma (RCC)
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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
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Merck (MRK) Announces FDA Approval of Expanded Monotherapy Label for its KEYTRUDA
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FDA Approves Expanded Monotherapy Label for Merck’s KEYTRUDA® (pembrolizumab)
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AstraZeneca (AZN) and Merck's (MRK) LYNPARZA Approved in EU for Treatment of Germline BRCA-Mutated HER2-Negative Advanced Breast Cancer
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LYNPARZA® (olaparib) Approved in EU for the Treatment of Germline BRCA-Mutated HER2-Negative Advanced Breast Cancer
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Myriad Genetics (MYGN), AstraZeneca (AZN) and Merck (MRK) Expand Companion Diagnostic Partnership
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Merck (MRK) Completes Tender Offer to Acquire Immune Design (IMDZ)
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Merck Completes Tender Offer to Acquire Immune Design
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Merck to Hold First-Quarter 2019 Sales and Earnings Conference Call on April 30
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Merck Completes Acquisition of Antelliq Corporation to Become Leader in Emerging Digital Technology for Livestock and Companion Animals

