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U.S. FDA Approves Pfizer’s Biosimilar NIVESTYM™ (filgrastim-aafi)
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Pfizer (PFE), Eli Lilly (LLY) Reports Positive Top-Line Results from Phase 3 Trial Of Tanezumab for Treatment of Osteoarthritis Pain
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Pfizer And Lilly Announce Positive Top-Line Results From Phase 3 Trial Of Tanezumab For The Treatment Of Osteoarthritis (OA) Pain
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Pfizer (PFE), Spark (ONCE) Initiate Pivotal Phase 3 Program for Investigational Hemophilia B Gene Therapy
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Pfizer Initiates Pivotal Phase 3 Program for Investigational Hemophilia B Gene Therapy
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Pfizer (PFE) Announces XELJANZ Received Marketing Authorisation in EU for Active Psoriatic Arthritis
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XELJANZ® (tofacitinib citrate) Receives Marketing Authorisation in the European Union for Active Psoriatic Arthritis
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Pfizer Declares 34-Cent Third-Quarter 2018 Dividend
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Pfizer (PFE) Secures Priority Review Designation and New Drug Application Acceptance for Glasdegib
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U.S. FDA Grants Priority Review for Pfizer’s New Drug Application for Glasdegib in Patients with Previously Untreated Acute Myeloid Leukemia
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Pfizer (PFE) Announces OS Results from Phase 3 PALOMA-3 Trial of IBRANCE in HR+, HER2- Metastatic Breast Cancer
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Pfizer Announces Overall Survival Results from Phase 3 PALOMA-3 Trial of IBRANCE® (Palbociclib) in HR+, HER2- Metastatic Breast Cancer
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Pfizer Announces Extension of Zithromax® Antibiotic Donation Program through 2025 to Help Eliminate World’s Leading Infectious Cause of Blindness
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Pfizer (PFE) Says FDA and EMA Accept Regulatory Submissions for Review of Talazoparib for Metastatic Breast Cancer Patients with an Inherited BRCA Mutation
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U.S. FDA and European Medicines Agency Accept Regulatory Submissions for Review of Talazoparib for Metastatic Breast Cancer Patients with an Inherited BRCA Mutation
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Pfizer (PFE) Expands Venture Investing with $600 Million Commitment to Pfizer Ventures
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Pfizer to Expand Venture Investing with $600 Million Commitment to Pfizer Ventures
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Pfizer (PFE) Reports Overall Survival Data from ARCHER 1050 Trial Evaluating Dacomitinib as First Line Treatment
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Dacomitinib Shows More than Seven-Month Improvement in Overall Survival Compared to an Established Therapy in Advanced NSCLC with EGFR-Activating Mutations
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Merck Provides Two-Year Update of Pivotal JAVELIN Merkel 200 Trial Showing Continued Durable Responses with BAVENCIO (avelumab)
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Two-Year Update of Pivotal JAVELIN Merkel 200 Trial Shows Continued Durable Responses with BAVENCIO® (avelumab)
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Pfizer (PFE) Reports Positive CHMP Opinion for Oncology Biosimilar, TRAZIMERA (trastuzumab)
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Pfizer Receives Positive CHMP Opinion for Oncology Biosimilar, TRAZIMERA™ (trastuzumab)
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Pfizer (PFE) Announces U.S. FDA Approves XELJANZ for Treatment of Moderately to Severely Active Ulcerative Colitis
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Pfizer Announces U.S. FDA Approves XELJANZ® (tofacitinib) for the Treatment of Moderately to Severely Active Ulcerative Colitis
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Pfizer (PFE) Says XALKORI Received FDA Breakthrough Therapy Designation in Two New Indications
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Pfizer’s XALKORI® (crizotinib) Receives FDA Breakthrough Therapy Designation in Two New Indications
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Pfizer (PFE) Says FDA Granted Breakthrough Therapy Designation for Tafamidis for Treatment of Patients with Transthyretin Cardiomyopathy
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FDA Grants Breakthrough Therapy Designation for Tafamidis for the Treatment of Patients with Transthyretin Cardiomyopathy
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A Study Analyzing Observational Data Shows Real-World Effectiveness of Prevnar® 13 in Adults Age 65+
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Pfizer (PFE) Begins a Phase 1/2 Study to Evaluate RSV Vaccine
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Pfizer Begins a Phase 1/2 Study to Evaluate Respiratory Syncytial Virus (RSV) Vaccine
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Spark Therapeutics (ONCE) and Pfizer (PFE) Highlight Data from Ongoing Phase 1/2 Clinical Trial of Investigational SPK-9001 for 15 Patients with Severe/Moderately-Severe Hemophilia B
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Spark Therapeutics and Pfizer Announce Data from 15 Participants with Hemophilia B Showing Persistent and Sustained Factor IX Levels with No Serious Adverse Events
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Spark Therapeutics and Pfizer Announce Data from 15 Participants with Hemophilia B Showing Persistent and Sustained Factor IX Levels with No Serious Adverse Events
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Spark Therapeutics and Pfizer Announce Data from 15 Participants with Hemophilia B Showing Persistent and Sustained Factor IX Levels with No Serious Adverse Events
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Pfizer (PFE) Says LYRICA Oral Solution CV Phase 3 Trial in Pediatric Epilepsy Met Primary Endpoint
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LYRICA® (pregabalin) Oral Solution CV Phase 3 Trial in Pediatric Epilepsy Meets Primary Endpoint
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Pfizer Oncology to Showcase Clinical Advances from its Growing Portfolio and Research Pipeline at ASCO
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Pfizer (PFE) Announces FDA Approval for Biosimilar RETACRIT
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Pfizer’s Biosimilar RETACRIT® (epoetin alfa-epbx) Approved by U.S. FDA
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Pfizer Hosts Annual Meeting of Shareholders
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Pfizer (PFE) Announces FDA Breakthrough Therapy Designation for TRUMENBA for Prevention of Invasive Meningococcal B Disease in Children Ages 1 to 9 Years
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Pfizer Granted FDA Breakthrough Therapy Designation for TRUMENBA® (Meningococcal Group B Vaccine) for the Prevention of Invasive Meningococcal B Disease in Children Ages 1 to 9 Years
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Pfizer (PFE) Receives CRL on Proposed Trastuzumab Biosimilar
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Pfizer Provides Update on Proposed Trastuzumab Biosimilar
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Pfizer (PFE) Announces MYLOTARG Was Approved in EU For Treatment Of Previously Untreated, De Novo, CD33-positive AML in Combination With Chemotherapy
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MYLOTARG™ Approved In The EU For The Treatment Of Previously Untreated, De Novo, CD33-positive Acute Myeloid Leukemia In Combination With Chemotherapy
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Pfizer Invites Public to Listen to Webcast of April 26 Annual Meeting of Shareholders
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Pfizer (PFE) Commences Phase 1b Clinical Trial for Investigational Mini-Dystrophin Gene Therapy, PF-06939926

