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Pfizer (PFE) Granted FDA Breakthrough Therapy Designation for Respiratory Syncytial Virus Vaccine Candidate for the Prevention of RSV in Infants from Birth up to Six Months of Age by Active Immunizati
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Pfizer Granted FDA Breakthrough Therapy Designation for Respiratory Syncytial Virus (RSV) Vaccine Candidate for the Prevention of RSV in Infants from Birth up to Six Months of Age by Active Immunizati
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Pfizer (PFE) Reports Phase 3 CLOVER Trial Results
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Phase 3 CLOVER Trial for Pfizer’s Investigational Clostridioides Difficile Vaccine Indicates Strong Potential Effect in Reducing Duration and Severity of Disease Based on Secondary Endpoints
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Biohaven Pharma (BHVN) Pfizer (PFE) Receive Positive CHMP Opinion for Migraine Treatment
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Biohaven and Pfizer Receive Positive CHMP Opinion for Migraine Treatment
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Keynote Presentation at Healthcare Conference
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Pfizer (PFE), OPKO’s (OPK) Once-Weekly NGENLA Injection Receives Marketing Authorization in European Union for Treatment of Pediatric GHD
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Pfizer and OPKO’s Once-Weekly NGENLA™ (somatrogon) Injection Receives Marketing Authorization in European Union for Treatment of Pediatric Growth Hormone Deficiency
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EMA Approves Pfizer’s (PFE) 20-Valent Pneumococcal Conjugate Vaccine Against Invasive Pneumococcal Disease and Pneumonia in Adults
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European Medicines Agency Approves Pfizer’s 20-Valent Pneumococcal Conjugate Vaccine Against Invasive Pneumococcal Disease and Pneumonia in Adults
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Biohaven Pharma (BHVN), Pfizer (PFE) Announce Positive Topline Results of Pivotal Trial of Rimegepant for the Acute Treatment of Migraine in China and South Korea
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Biohaven and Pfizer Announce Positive Topline Results of Pivotal Trial of Rimegepant for the Acute Treatment of Migraine in China and South Korea
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Pfizer (PFE)/BioNTech (BNTX) Provide Update on Rolling Submission for EAU for COVID-19 Vaccine for Children
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Pfizer and BioNTech Provide Update on Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age
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Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer (PFE) and Valneva (VALN) Report Additional Positive Phase 2 Data for Lyme Disease Vaccine Candidate
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Valneva and Pfizer Report Further Positive Phase 2 Data for Lyme Disease Vaccine Candidate
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Pfizer and BioNTech Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age Following Request from U.S. FDA
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Pfizer (PFE) and BioNTech (BNTX) Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4
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Pfizer and BioNTech Initiate Rolling Submission for Emergency Use Authorization of Their COVID-19 Vaccine in Children 6 Months Through 4 Years of Age Following Request From U.S. FDA
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Pfizer (PFE) Announces New Chief Development Officer
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Pfizer Announces New Chief Development Officer
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Pfizer (PFE), Ionis (IONS) announce discontinuation of vupanorsen clinical development program
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Pfizer and Ionis announce discontinuation of vupanorsen clinical development program
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Pfizer (PFE) Announces European Commission Approves LORVIQUA as First-Line Treatment for ALK-Positive Advanced Lung Cancer
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European Commission Approves LORVIQUA® (lorlatinib) as a First-Line Treatment for ALK-Positive Advanced Lung Cancer
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Pfizer (PFE) Announces Positive CHMP Opinion for COVID-19 Oral Treatment
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Pfizer Receives CHMP Positive Opinion for Novel COVID-19 Oral Treatment
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Pfizer (PFE), BioNTech (BNTX) Initiate Study to Evaluate Omicron-Based COVID-19 Vaccine in Adults
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Pfizer and BioNTech Initiate Study to Evaluate Omicron-Based COVID-19 Vaccine in Adults 18 to 55 Years of Age
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Pfizer and BioNTech Initiate Study to Evaluate Omicron-Based COVID-19 Vaccine in Adults 18 to 55 Years of Age
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Pre-Open Stock Movers 01/24: (EXTN) (KSS) (UL) Higher; (OPK) (MSTR) (MARA) Lower (more...)
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Pfizer (PFE) and OPKO (OPK) Receive CRL for BLA for Somatrogon for Pediatric Growth Hormone Deficiency
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Pfizer and OPKO Provide Update on the Biologics License Application for Somatrogon for Pediatric Growth Hormone Deficiency
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OPKO Health (OPK) and Pfizer (PFE) Announce Approval of NGENLA in Japan
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Japan’s MHLW Approves Pfizer and OPKO’s NGENLA® (Somatrogon), a New Long-Acting Treatment for Pediatric Growth Hormone Deficiency
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Pfizer (PFE) Announces U.S. FDA Approves CIBINQO for Adults with Moderate-to-Severe Atopic
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U.S. FDA Approves Pfizer’s CIBINQO® (abrocitinib) for Adults with Moderate-to-Severe Atopic Dermatitis
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Pfizer (PFE) Reports Positive Top-Line Results of Phase 3 Study Exploring Coadministration of PREVNAR 20 With Pfizer-BioNTech COVID-19 Vaccine in Older Adults Released
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Positive Top-Line Results of Pfizer’s Phase 3 Study Exploring Coadministration of PREVNAR 20™ With Pfizer-BioNTech COVID-19 Vaccine in Older Adults Released
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Becton Dickinson (BDX), Pfizer (PFE) and Wellcome Collaborate to Improve Global Hospital Antimicrobial Stewardship Practices
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Pfizer (PFE) Enters Pact with Acuitas Therapeutics for Lipid Nanoparticle Delivery System for Use in mRNA Vaccines and Therapeutics
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Pfizer Enters into Agreement with Acuitas Therapeutics for Lipid Nanoparticle Delivery System for Use in mRNA Vaccines and Therapeutics
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Pfizer (PFE) Enters Exclusive Collaboration with Beam (BEAM) for Novel In Vivo Base Editing Programs for a Range of Rare Diseases
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Pfizer and Beam Enter Exclusive Multi-Target Research Collaboration to Advance Novel In Vivo Base Editing Programs for a Range of Rare Diseases
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Pfizer and Beam Enter Exclusive Multi-Target Research Collaboration to Advance Novel In Vivo Base Editing Programs for a Range of Rare Diseases
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Pfizer and Beam Enter Exclusive Multi-Target Research Collaboration to Advance Novel In Vivo Base Editing Programs for a Range of Rare Diseases
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Biohaven Pharma (BHVN), Pfizer (PFE) Complete Collaboration Transaction for Commercialization of Rimegepant and Zavegepant Outside United States

