http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Basilea announces license agreement with Pfizer for antifungal Cresemba® (isavuconazole) for Europe, Russia, Turkey and Israel
-
Nearly One in Four New and Expectant Parents Have Never Heard of Invasive Pneumococcal Disease According to a New Survey
-
Pfizer (PFE) and Lilly (LLY) Announce FDA Fast Track Designation for Tanezumab
-
Pfizer and Lilly Receive FDA Fast Track Designation for Tanezumab
-
Merck and Pfizer Announce that Investigational SGLT-2 Inhibitor Ertugliflozin Met Primary Endpoint in Two Phase 3 Studies
-
Sangamo Biosciences (SGMO) & Pfizer (PFE) Granted Orphan Medicinal Product Designation from European Medicines Agency for SB-525 Investigational Hemophilia A Gene Therapy
-
Sangamo Therapeutics And Pfizer Announce That SB-525 Investigational Hemophilia A Gene Therapy Receives Orphan Medicinal Product Designation From The European Medicines Agency
-
Pfizer (PFE) Receives FDA Fast Track Designation for Tafamidis to Treat TTR-CM
-
Pfizer Receives FDA Fast Track Designation for Tafamidis for Transthyretin Cardiomyopathy
-
Pfizer Presents Final Phase 2 Data on Investigational PARP Inhibitor Talazoparib in Patients with Germline BRCA-Positive Advanced Breast Cancer
-
Pfizer (PFE) sNDA for SUTENT Accepted by FDA, EMA; January 2018 PDUFA
-
Pfizer Announces Acceptance of Regulatory Submissions by U.S. FDA and European Medicines Agency for SUTENT® (sunitinib) for Adjuvant Treatment of Adult Patients at High Risk of Recurrent Renal Cell C
-
Pfizer (PFE) Announces EC Approval for TRUMENBA to Help Prevent Meningococcal Group B Disease in Adolescents and Adults
-
European Commission Approves Pfizer’s TRUMENBA® to Help Prevent Meningococcal Group B Disease in Adolescents and Adults
-
Pfizer (PFE) Announces FDA AdCom Recommendation for Epogen/Procrit Biosimilar
-
FDA Advisory Committee Recommends Approval of Pfizer’s Proposed Biosimilar to Epogen®/Procrit® Across All Indications
-
Pfizer Recommends Shareholders Reject the Below-Market Mini-Tender Offer by TRC Capital Corporation
-
Pfizer Oncology to Present Data Across 13 Different Types of Cancer at ASCO 2017 Annual Meeting
-
Sangamo Biosciences (SGMO), Pfizer (PFE) Enter Pact on Hemophilia A Gene Therapy
-
Sangamo Therapeutics And Pfizer Announce Collaboration For Hemophilia A Gene Therapy
-
Merck KGaA, Pfizer (PFE) Announce FDA Approval for BAVENCIO for Common Type of Advanced Bladder Cancer
-
FDA Grants BAVENCIO® (avelumab) Approval for a Common Type of Advanced Bladder Cancer
-
Collaboration Helps Broaden Access to Pfizer’s Contraceptive, Sayana® Press (medroxyprogesterone acetate), for Women in Some of the World’s Poorest Countries
-
Phase 3 OCTAVE Studies of Oral Tofacitinib in Ulcerative Colitis Results Published in The New England Journal of Medicine
-
Pfizer (PFE) Announces FDA Filing Acceptance of sNDA for XELJANZ to Treat Adults with PsA
-
Pfizer Announces U.S. FDA Filing Acceptance of Supplemental New Drug Application for XELJANZ® (tofacitinib citrate) for the Treatment of Adult Patients with Active Psoriatic Arthritis
-
Pfizer Hosts Annual Meeting of Shareholders
-
InSphero Announces Agreement with Pfizer to Develop Novel Assays for Predicting Drug-induced Liver Injury
-
Pfizer's (PFE) Lorlatinib Granted Breakthrough Therapy Designation from FDA for ALK-Positive Metastatic NSCLC
-
Pfizer’s Next-Generation ALK/ROS1 Inhibitor, Lorlatinib, Granted Breakthrough Therapy Designation from FDA for ALK-Positive Metastatic Non-Small Cell Lung Cancer
-
Pfizer (PFE) Announce Topline Phase III Study Results for Efficacy Of Zavicefta (Ceftazidime-Avibactam) for Treatment Of Hospital-Acquired Pneumonia
-
Pivotal Phase III Study Underscores Efficacy Of Zavicefta™ (ceftazidime-avibactam) For Treatment Of Hospital-Acquired Pneumonia, A Leading Cause Of Mortality In Hospitals
-
Pfizer (PFE) Announces Positive CHMP Opinion for BESPONSA to Treat Relapsed/Refractory ALL
-
Pfizer Receives Positive CHMP Opinion for BESPONSA® (Inotuzumab Ozogamicin) for the Treatment of Relapsed or Refractory Acute Lymphoblastic Leukemia
-
Pfizer Unveils ATLAS®, An Interactive, User-Friendly Website That Provides Global Antibiotic Resistance Surveillance Data Across 60 Countries
-
Pfizer (PFE) & HitGen Report 4-yr Agreement to Build and Screen Novel DNA-Encoded Libraries
-
HitGen and Pfizer Enter Research Collaboration and License Agreement to Build and Screen Novel DNA-Encoded Libraries
-
Pfizer (PFE) Announces Expanded FDA Approval for IBRANCE Indication for First-Line HR+, HER2- Metastatic Breast Cancer
-
IBRANCE® (palbociclib) Receives FDA Regular Approval and Expanded Indication for First-Line HR+, HER2- Metastatic Breast Cancer
-
Pfizer (PFE) Secures EC Marketing Authorization for Treatment of Rheumatoid Arthritis
-
XELJANZ® (tofacitinib citrate) Receives Marketing Authorisation in the European Union for the Treatment of Moderate to Severe Active Rheumatoid Arthritis (RA)
-
Pfizer (PFE) Announces Positive CHMP Opinion for TRUMENBA for Prevention of Meningococcal Group B Disease
-
Pfizer Receives Positive CHMP Opinion for TRUMENBA® for Prevention of Meningococcal Group B Disease
-
Pfizer (PFE) and Merck (MRK) BioPharma Unit Get FDA Approval for BAVENCIO® (Avelumab), the 1st Immunotherapy Approved for Metastatic Merkel Cell Carcinoma
-
FDA Grants Approval for BAVENCIO® (avelumab), the First Immunotherapy Approved for Metastatic Merkel Cell Carcinoma
-
Bristol-Myers Squibb (BMY), Pfizer (PFE) Present Analysis of Effectiveness and Safety of Direct Oral Anticoagulants Compared to Warfarin in Patients with Non-Valvular Atrial Fibrillation
-
Bristol-Myers Squibb and Pfizer Present Large Real-World Observational Analysis of the Effectiveness and Safety of Direct Oral Anticoagulants Compared to Warfarin in Patients with Non-Valvular Atrial
-
Pfizer (PFE) Announces Approval of XELJANZ�® by the China FDA
-
Pfizer Announces Approval By The China Food And Drug Administration Of XELJANZ®, The First Oral JAK Inhibitor For Adult Patients With Moderately To Severely Active Rheumatoid Arthritis
-
Pfizer (PFE) Launches Zavicefta in the U.K. and Germany

