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Pfizer Postpones Investor Day Scheduled for March 31, 2020 Due to Coronavirus Concerns
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Pfizer (PFE) Announces Top-Line Results from Phase 3 Study of 20-Valent Pneumococcal Conjugate Vaccine in Pneumococcal Vaccine-Naïve Adults Aged 18 Years or Older
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Pfizer (PFE) Phase 3 trial of abrocitinib for moderate to severe atopic dermatitis met all co-primary endpoints
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Pfizer Announces Top-Line Results from Phase 3 Study of 20-Valent Pneumococcal Conjugate Vaccine in Pneumococcal Vaccine-Naïve Adults Aged 18 Years or Older
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Pfizer Announces Positive Top-Line Results from Third Phase 3 Trial of Abrocitinib for Moderate to Severe Atopic Dermatitis, Which Showed Improvements in Skin Clearance, Disease Extent and Severity,
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Pfizer Invites Public to View and Listen to Webcast of April 28 Conference Call with Analysts
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Pfizer (PFE) and BioNTech SE (BNTX) Agree to Co-Develop Potential COVID-19 Vaccine
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Pfizer and BioNTech to Co-develop Potential COVID-19 Vaccine
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Pfizer and BioNTech to Co-Develop Potential COVID-19 Vaccine
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Germany tries to halt U.S. interest in firm working on coronavirus vaccine
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Pfizer (PFE) Outlines Five-Point Plan to Battle COVID-19
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Pfizer Outlines Five-Point Plan to Battle COVID-19
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EMD Serono and Pfizer (PFE) Provide Update on Phase III JAVELIN Head and Neck 100 Study
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EMD Serono and Pfizer Provide Update on Phase III JAVELIN Head and Neck 100 Study
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Pfizer (PFE) Reports Election of Susan Hockfield to Board
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Susan Hockfield Elected to Pfizer’s Board of Directors
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Pfizer (PFE) and Lilly (LLY) announce FDA accepted for review BLA for tanezumab 2.5 mg administered subcutaneously
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U.S. FDA Accepts Regulatory Submission for Tanezumab, a Potential First-in-Class Treatment for Patients with Chronic Pain Due to Moderate-to-Severe Osteoarthritis
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James Quincey Elected to Pfizer’s Board of Directors
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Mylan and Pfizer Announce Appointment of Viatris Chief Financial Officer
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Mylan and Pfizer Announce Appointment of Viatris Chief Financial Officer
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Mylan and Pfizer Finalize Appointments to Viatris Board of Directors
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Mylan and Pfizer Finalize Appointments to Viatris Board of Directors
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Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
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European Commission Approves VYNDAQEL®, the First Treatment in the EU for Transthyretin Amyloid Cardiomyopathy (ATTR-CM)
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Pfizer (PFE) Receives Positive CHMP Opinion for Oncology Biosimilar, RUXIENCE
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Pfizer Receives Positive CHMP Opinion for Oncology Biosimilar, RUXIENCE™ (rituximab)
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Pfizer Vaccines Launches Global Centers of Excellence Network to Conduct Real-World Research on Vaccine-Preventable Diseases Affecting Adults
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Pfizer’s Greenstone and Digital Men’s Health Clinic Roman Collaborate to Offer Patients Remote Access to the Only FDA-Approved Authorized Generic Version of Viagra® (sildenafil citrate)
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Biogen (BIIB) to Acquire Novel Clinical Stage Asset with Application in Alzheimer's Disease and Parkinson's Disease from Pfizer Inc. (PFE)
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Biogen to Acquire Novel Clinical Stage Asset with Application in Alzheimer’s Disease and Parkinson’s Disease from Pfizer Inc.
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Biogen to Acquire Novel Clinical Stage Asset with Application in Alzheimer’s Disease and Parkinson’s Disease from Pfizer Inc.
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Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
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EMD Serono, Pfizer (PFE) Announce BAVENCIO Significantly Improved Overall Survival in Patients With Locally Advanced or Metastatic Urothelial Carcinoma
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BAVENCIO Significantly Improved Overall Survival in Patients With Locally Advanced or Metastatic Urothelial Carcinoma
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Theravance Biopharma (TBPH), Pfizer (PFE) Enter Pact for Skin-Targeted, Locally-Acting Pan-Janus Kinase Inhibitor Program
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Theravance Biopharma and Pfizer Inc. Enter Global License Agreement for Skin-Targeted, Locally-Acting Pan-Janus Kinase (JAK) Inhibitor Program
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Pfizer (PFE) Reports FDA Accepts & Grants Priority Review to sNDA for BRAFTOVI (encorafenib) in Combination with ERBITUX (cetuximab) (BRAFTOVI Doublet)
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U.S. FDA Accepts and Grants Priority Review to sNDA for BRAFTOVI® (encorafenib) in Combination with ERBITUX® (cetuximab) (BRAFTOVI Doublet) for the Treatment of BRAFV600E-Mutant Metastatic Colorecta
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Pfizer and Mylan Announce Two Future Viatris Board Members
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Pfizer and Mylan Announce Two Future Viatris Board Members
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Pfizer Invites Public to View and Listen to Webcast of January 28 Conference Call with Analysts
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Pfizer Declares First-Quarter 2020 Dividend and Announces Upcoming Investor Day to Highlight Strength of Innovative R&D Pipeline
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Pfizer (PFE) Reports Positive CHMP Opinion for VYNDAQEL for Use in Patients with Transthyretin Amyloid Cardiomyopathy
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Pfizer Receives Positive CHMP Opinion for VYNDAQEL® for Use in Patients with Transthyretin Amyloid Cardiomyopathy, a Rare and Fatal Disease
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Pfizer (PFE) Announces FDA Approves XELJANZ XR (tofacitinib) Extended-Release Tablets for Treatment of Ulcerative Colitis
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FDA Approves XELJANZ® XR (tofacitinib) Extended-Release Tablets for the Treatment of Ulcerative Colitis
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Sangamo Therapeutics (SGMO), Pfizer (PFE) Report Updated Follow-Up Results from Phase 1/2 Alta Study Evaluating Investigational SB-525 Gene Therapy
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Sangamo and Pfizer Announce Updated Phase 1/2 Results Showing Sustained Increased Factor VIII Activity Through 44 Weeks Following SB-525 Gene Therapy Treatment
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Akcea and Ionis Announce Closing of Licensing Agreement with Pfizer Inc. for Investigative Antisense Therapy AKCEA-ANGPTL3-L(Rx)

