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Pfizer Doses First Patient Using Investigational Mini-Dystrophin Gene Therapy for the Treatment of Duchenne Muscular Dystrophy
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Pfizer (PFE) Says DMC Recommends Stopping Phase 3 Trial of Axitinib as Adjuvant Treatment for Patients at High Risk of RCC Recurrence After Surgery
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Pfizer Provides Update on Phase 3 Trial of Axitinib as Adjuvant Treatment for Patients at High Risk of Renal Cell Carcinoma Recurrence After Surgery
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Pfizer Signs Lease for the Spiral at Hudson Yards in Manhattan
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Allogene Therapeutics Completes Agreement for Pfizer’s Allogeneic CAR T Immuno-oncology Portfolio
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Pfizer Canada and MaRS Innovation Partner to Convert Great Science into Solutions to Benefit Canadians’ Health
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Pfizer (PFE) Says U.S. FDA and EMA Accept Regulatory Submissions for Review of Dacomitinib to Treat Metastatic NSCLC with EGFR-Activating Mutations
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U.S. FDA and European Medicines Agency Accept Regulatory Submissions for Review of Dacomitinib to Treat Metastatic Non-Small Cell Lung Cancer with EGFR-Activating Mutations
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Pfizer (PFE) and Allogene Therapeutics Enter Pact for Pfizer's Allogeneic CAR T Immuno-oncology Portfolio
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Pfizer and Allogene Therapeutics Enter into Asset Contribution Agreement for Pfizer’s Allogeneic CAR T Immuno-oncology Portfolio
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Pfizer (PFE) Reports Topline Results From Phase 3 ATTR-ACT Study Of Tafamidis to Treat Transthyretin Cardiomyopathy
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Pfizer Announces Positive Topline Results From Phase 3 ATTR-ACT Study Of Tafamidis In Patients With Transthyretin Cardiomyopathy
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Pfizer (PFE) Announces Top-Line Results from Study of CHANTIX/CHAMPIX (varenicline) in Adolescent Smokers
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Pfizer Reports Top-Line Results from a Study of CHANTIX®/CHAMPIX® (varenicline) in Adolescent Smokers
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Biogen to Acquire from Pfizer First-in-Class Phase 2b Ready Asset for Cognitive Impairment Associated with Schizophrenia
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Findings Released from Largest Real-World Data Analysis of Non-Valvular Atrial Fibrillation Patients Receiving Direct Oral Anticoagulants
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Pfizer (PFE) Confirms Favorable Outcome of FDA Panel Meeting on XELJANZ for Moderately to Severely Active UC
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Pfizer Announces Favorable Outcome of FDA Advisory Committee Meeting on XELJANZ® (tofacitinib) for Moderately to Severely Active Ulcerative Colitis
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Cellectis: Servier and Pfizer Announce Results of UCART19 First-in-Human Trials to Be Presented at the 44th EBMT (European Society for Blood and Marrow Transplantation) Annual Meeting
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Pfizer (PFE) Appoints Dan Littman to Board
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Dan R. Littman Elected to Pfizer’s Board of Directors
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Pfizer (PFE) Reports Positive CHMP Opinion for MYLOTARG & BOSULIF
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Pfizer Receives Positive CHMP Opinion for Two Hematology Medicines, MYLOTARG™ and BOSULIF®
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Pfizer (PFE) Reports Update on EMA Application for SUTENT (sunitinib)
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Pfizer Announces Update on European Marketing Authorization Application for SUTENT® (sunitinib) in Adult Patients at High Risk of Recurrent Renal Cell Carcinoma
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Pfizer (PFE) Announces Election of Albert Bourla, DVM, Ph.D. to Board
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Albert Bourla Elected to Pfizer’s Board of Directors
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Merck KGaA, Pfizer (PFE) Provide Update on Phase III JAVELIN Lung 200 Trial of Avelumab Monotherapy in Previously Treated Patients with Advanced NSCLC
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Merck KGaA, Darmstadt, Germany, and Pfizer Provide Update on Phase III JAVELIN Lung 200 Trial of Avelumab Monotherapy in Previously Treated Patients with Advanced Non-Small Cell Lung Cancer
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Pfizer (PFE) Reports Breakthrough Therapy Designation from FDA for PF-04965842
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Pfizer Receives Breakthrough Therapy Designation from FDA for PF-04965842, an oral JAK1 Inhibitor, for the Treatment of Patients with Moderate-to-Severe Atopic Dermatitis
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Pfizer (PFE) Says U.S., EU and Japan Health Authorities Accept Regulatory Submissions for Review of its Third-Generation ALK Inhibitor Lorlatinib
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U.S., EU and Japan Health Authorities Accept Regulatory Submissions for Review of Pfizer’s Third-Generation ALK Inhibitor Lorlatinib
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NetVation DL Medicine Announces Research Collaboration with Pfizer Inc.
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NetVation DL Medicine Announces Research Collaboration with Pfizer Inc.
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Pfizer (PFE) Reports Positive Top-Line Results For Potential Biosimilar To Rituxan/MabThera
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Pfizer Announces Positive Top-Line Results For Potential Biosimilar To Rituxan®/MabThera®
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Foundation Medicine (FMI), Pfizer (PFE) Announce Pact to Develop Companion Diagnostics for Pfizer's Oncology Portfolio
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Foundation Medicine and Pfizer Announce Broad Partnership to Develop Companion Diagnostics for Pfizer’s Oncology Portfolio
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Pfizer (PFE) Announces New Partnership Model for Early-Stage Academic Research
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Pfizer Establishes New Partnering Model for Early-Stage Academic Research
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Sangamo Therapeutics (SGMO) and Pfizer (PFE) Announced Collaboration for ALS Treatments; $12M Upfront
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Sangamo and Pfizer announce collaboration for development of zinc finger protein gene therapy for ALS
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Merck (MRK) and Pfizer (PFE) Announce FDA Approval of SGLT2 Inhibitor STEGLATRO and Fixed-Dose Combination STEGLUJAN for Adults with Type 2 Diabetes
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FDA Approves SGLT2 Inhibitor STEGLATRO™ (ertugliflozin) and Fixed-Dose Combination STEGLUJAN™ (ertugliflozin and sitagliptin) for Adults with Type 2 Diabetes
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Merck (MRK) and Pfizer (PFE) Granted FDA Breakthrough Therapy Designation for Avelumab, INLYTA Combo in Advanced Renal Cell Carcinom
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FDA Grants Breakthrough Therapy Designation for Avelumab in Combination with INLYTA® in Advanced Renal Cell Carcinoma
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FDA Grants Breakthrough Therapy Designation for Avelumab in Combination with INLYTA® in Advanced Renal Cell Carcinoma
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Pfizer (PFE) Granted FDA Approves BOSULIF (bosutinib) for the Treatment of Patients with Newly-Diagnosed Ph+ Chronic Myelogenous Leukemia
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U.S. FDA Approves Pfizer’s BOSULIF® (bosutinib) for the Treatment of Patients with Newly-Diagnosed Ph+ Chronic Myelogenous Leukemia (CML)

