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Pfizer Declares First-Quarter 2018 Dividend
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Pfizer (PFE) Granted FDA Approval of XELJANZ (tofacitinib) and XELJANZ XR for Treatment of Active Psoriatic Arthritis
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Pfizer Announces FDA Approval of XELJANZ® (tofacitinib) and XELJANZ® XR for the Treatment of Active Psoriatic Arthritis
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Pfizer (PFE) Begins Phase 3 Program for PF-04965842 for Moderate-to-Severe Atopic Dermatitis
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Pfizer Initiates Phase 3 Program for PF-04965842, a JAK1 Inhibitor in Development for Moderate-to-Severe Atopic Dermatitis
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Pfizer (PFE) Announces FDA Approval for Remicade Biosimilar
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FDA Approves New Pfizer Biosimilar
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Pfizer (PFE) Highlights Data on Phase 3 TRUMENBA (Meningococcal Group B Vaccine)
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Phase 3 TRUMENBA® (Meningococcal Group B Vaccine) Data Published in New England Journal of Medicine Demonstrate the Vaccine’s Immunogenicity
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Preliminary Data from Servier and Pfizer’s UCART19 Product Candidate Shows High Complete Remission Rate Across Two Phase I Adult and Pediatric Acute Lymphoblastic Leukemia Trials
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Pfizer (PFE) Reports FDA Extended Action Date For XELJANZ sNDA in Ulcerative Colitis By Three Months
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U.S. Food And Drug Administration Extends Action Date For XELJANZ® (Tofacitinib) Supplemental New Drug Application In Ulcerative Colitis By Three Months
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Spark Therapeutics (ONCE) and Pfizer (PFE) Announce L-T Prelim. Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at ASH Meeting
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Spark Therapeutics and Pfizer Announce Longer-term Preliminary Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at 59th American Society of Hematology (ASH) Annual Meeting and Ex
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Spark Therapeutics and Pfizer Announce Longer-term Preliminary Data Showing Consistent and Sustained Factor IX Levels in Hemophilia B at 59th American Society of Hematology (ASH) Annual Meeting and Ex
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Pfizer (PFE) Announces Talazoparib Significantly Extends PFS in Phase 3 EMBRACA Trial of Patients with Metastatic Breast Cancer
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Talazoparib Significantly Extends Progression-Free Survival in Phase 3 EMBRACA Trial of Patients with Metastatic Breast Cancer
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Spark Therapeutics (ONCE), Pfizer (PFE) Announce Publication in NEJM of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Spark Therapeutics and Pfizer Announce Publication in The New England Journal of Medicine of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Spark Therapeutics and Pfizer Announce Publication in The New England Journal of Medicine of Interim Data from Phase 1/2 Clinical Trial of Investigational Gene Therapy for Hemophilia B
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Pfizer (PFE) Says Updated Data from Phase 3 Trial of IBRANCE Plus Letrozole in ER+, HER2- Metastatic Breast Cancer Confirm Improvement in PFS
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Updated Data from Phase 3 Trial of IBRANCE® (palbociclib) Plus Letrozole in ER+, HER2- Metastatic Breast Cancer Confirm Improvement in Progression-Free Survival
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Bristol-Myers Squibb and Pfizer Alliance Urge People to ‘Tune in to AFib, Take Note of Stroke Risk’
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Pfizer (PFE) Reports Agreement with Basilea Pharmaceutica Ltd to Develop and Commercialize CRESEMBA (isavuconazole) in China and Asia Pacific Region
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Pfizer Enters into Agreement to Develop and Commercialize CRESEMBA® (isavuconazole) in China and Asia Pacific Region
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Merck KGaA, Darmstadt, Germany, and Pfizer Provide Update on Phase III JAVELIN Gastric 300 Study in Patients with Pre-Treated Advanced Gastric Cancer
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Merck (MRK) and Pfizer (PFE) Announce Phase III JAVELIN Gastric 300 Study in Patients With Pre-Treated Advanced Gastric Cancer Did Not Meet Primary Endpoint
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Merck and Pfizer Provide Update on Phase III JAVELIN Gastric 300 Study in Patients With Pre-Treated Advanced Gastric Cancer
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Pfizer (PFE) Granted FDA Approval for SUTENT (sunitinib malate)
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Pfizer Receives FDA Approval for SUTENT® (sunitinib malate) as First and Only Adjuvant Treatment for Adult Patients at High Risk of Recurrent Renal Cell Carcinoma
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BMS (BMY)-Pfizer (PFE) Alliance to Unveil Real-World Data Analyses Associated with Oral Anticoagulants in NVAF
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BMS-Pfizer Alliance to Unveil Real-World Data Analyses - Cost, Safety and Comparative Effectiveness Findings Associated with Oral Anticoagulants in Non-Valvular Atrial Fibrillation
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Spark Therapeutics (ONCE), Pfizer (PFE) Amend Pact for Investigational SPK-9001 in Hemophilia B
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Spark Therapeutics and Pfizer Amend License Agreement for Investigational SPK-9001 in Hemophilia B
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Servier and Pfizer Announce Preliminary Results of the First-in-Human Trials of UCART19 Will Be Presented at the 59th American Society of Hematology (ASH) Annual Meeting
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One Year Maintenance and Switching Data in Patients with Crohn’s Disease Support the Use of INFLECTRA®* (infliximab CT-P13) in IBD¹
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Corning to Showcase Latest in Pharmaceutical Glass Technologies at CPhI Worldwide in Frankfurt, Germany
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Pfizer (PFE) Reports Phase 2 Study of Next-Generation Investigational ALK-Inhibitor Lorlatinib in ALK-Positive and ROS1-Positive Advanced Non-Small Cell Lung Cancer
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Pfizer Presents Full Results from Phase 2 Study of Next-Generation Investigational ALK-Inhibitor Lorlatinib in ALK-Positive and ROS1-Positive Advanced Non-Small Cell Lung Cancer
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Pfizer (PFE) Granted FDA Approval for LYRICA CR (Pregabalin)
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U.S. FDA Approves LYRICA® CR (pregabalin) Extended-Release Tablets CV
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Pfizer (PFE) Says it's Reviewing Strategic Alternatives for Consumer Healthcare Business
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Pfizer Reviewing Strategic Alternatives for Consumer Healthcare Business
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Pfizer Launches Novel Programs to Put Important Support Services at the Fingertips of Cancer Patients
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Pfizer Declares 32-Cent Fourth-Quarter 2017 Dividend
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Merck KGaA, Pfizer (PFE) Announce Bavencio Approval for Merkel Cell Carcinoma in Japan
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Bavencio (avelumab) Approved for Merkel Cell Carcinoma in Japan
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Patti LaBelle and Pfizer Work Together to Educate Baby Boomers About the Risk of Pneumococcal Pneumonia
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SpringWorks Therapeutics Launches with $103M in Series A Funding and Rights to Four Clinical Programs
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National Sickle Cell Disease Poll of African Americans Dispels Long-Held Views

