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Pfizer Completes Acquisition of Biohaven Pharmaceuticals
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BioNTech SE (BNTX) and Pfizer (PFE) Submit FDA Application for EMA of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children Aged 5-11
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Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children 5 Through 11 Years of Age
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Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children 5 Through 11 Years of Age
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Pfizer Declares Fourth-Quarter 2022 Dividend
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Pfizer to Supply Global Fund Up to 6 Million PAXLOVID™ Treatment Courses for Low-and-Middle-Income Countries
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Pfizer Invites Public to View and Listen to Webcast of November 1 Conference Call with Analysts
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Pfizer (PFE) Reports Positive Top-Line Results from Phase 3 Study in 20-Valent Pneumococcal Conjugate Vaccine in Infants in EU
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Pfizer Announces Positive Top-Line Results from Phase 3 Study in 20-Valent Pneumococcal Conjugate Vaccine in Infants in the European Union
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Pfizer (PFE), BioNTech (BNTX) Receive Positive CHMP Opinion for Conversion of COMIRNATY® Conditional Marketing Authorization to Full Marketing Authorization in the European Union
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Pfizer and BioNTech Receive Positive CHMP Opinion for Conversion of COMIRNATY® Conditional Marketing Authorization to Full Marketing Authorization in the European Union
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Pfizer (PFE) Reports Positive Top-Line Results from Phase 3 Trial of MenABCWY
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Pfizer Announces Positive Top-Line Results from Phase 3 Trial of Pentavalent Meningococcal Vaccine Candidate (MenABCWY) in Adolescents
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Pfizer Invites Public to View and Listen to Webcast of Analyst and Investor Call to Review Oral GLP-1 Data Presented at European Association for the Study of Diabetes (EASD) 2022
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Pfizer (PFE) Initiates Phase 3 Study of mRNA-Based Influenza Vaccine
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Pfizer Initiates Phase 3 Study of mRNA-Based Influenza Vaccine
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Pfizer (PFE), BioNTech (BNTX) Receive Positive CHMP Opinion for Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine Booster in European Union
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Pfizer and BioNTech Receive Positive CHMP Opinion for Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine Booster in European Union
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Pfizer and BioNTech Receive Positive CHMP Opinion for Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine Booster in European Union
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Pfizer (PFE) Announces FDA and EMA Acceptance of Ritlecitinib for Alopecia Areata
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FDA and EMA Accept Regulatory Submission for Pfizer’s Ritlecitinib for Individuals 12 Years and Older with Alopecia Areata
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Pfizer (PFE) Group B Streptococcus Vaccine Candidate Granted FDA Breakthrough Therapy Designation
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FDA Grants Breakthrough Therapy Designation to Pfizer’s Group B Streptococcus Vaccine Candidate to Help Prevent Infection in Infants Via Immunization of Pregnant Women
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer Invites Public to View and Listen to a Webcast of Pfizer Discussion on Climate Action
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Pfizer Invites Public to View and Listen to Two Webcasts of Pfizer Discussions at Healthcare Conferences
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BioNTech SE (BNTX) and Pfizer (PFE) Receive Positive CHMP Opinion for COVID-19 Vaccine Booster in EU
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Pfizer and BioNTech Receive Positive CHMP Opinion for Omicron BA.1-Adapted Bivalent COVID-19 Vaccine Booster in European Union
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Pfizer and BioNTech Receive Positive CHMP Opinion for Omicron BA.1-Adapted Bivalent COVID-19 Vaccine Booster in European Union
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Pfizer and BioNTech Granted FDA Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine Booster for Ages 12 Years and Older
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Pfizer (PFE), BioNTech SE (BNTX) Confirm FDA EUA for Omicron Booster
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Pfizer and BioNTech Granted FDA Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine Booster for Ages 12 Years and Older
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Pfizer and BioNTech Complete Submission to European Medicines Agency for Omicron BA.4/BA.5 Adapted Bivalent Vaccine
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Pfizer and BioNTech Complete Submission to European Medicines Agency for Omicron BA.4/BA.5 Adapted Bivalent Vaccine
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Pfizer (PFE) Reports Positive Top-Line Data from Phase 3 Trial of Older Adults for its Bivalent Respiratory Syncytial Virus (RSV) Vaccine Candidate
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Pfizer Announces Positive Top-Line Data from Phase 3 Trial of Older Adults for its Bivalent Respiratory Syncytial Virus (RSV) Vaccine Candidate
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Pfizer (PFE) and BioNTech (BNTX) Report Updated COVID-19 Vaccine Data Supporting Efficacy in Children 6 Months through 4 Years Old
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Pfizer and BioNTech Announce Updated COVID-19 Vaccine Data Supporting Efficacy in Children 6 Months through 4 Years of Age
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Pfizer and BioNTech Announce Updated COVID-19 Vaccine Data Supporting Efficacy in Children 6 Months through 4 Years of Age
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BioNTech SE (BNTX) and Pfizer (PFE) Submit FDA Application for EMA of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine
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Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine
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Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent COVID-19 Vaccine
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Discussion at Healthcare Conference
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ProMIS Neurosciences Announces Second Quarter 2022 Financial and Operating Results
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Pfizer (PFE) Reports Positive Top-Line Results from Phase 3 Study of 20-Valent Pneumococcal Conjugate Vaccine in Infants
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Pfizer Announces Positive Top-Line Results from Phase 3 Study of 20-Valent Pneumococcal Conjugate Vaccine in Infants
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Pfizer (PFE) and Valneva (VALN) Initiate Phase 3 Study of VLA15
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Pfizer and Valneva Initiate Phase 3 Study of Lyme Disease Vaccine Candidate VLA15
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Pfizer and Valneva Initiate Phase 3 Study of Lyme Disease Vaccine Candidate VLA15
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Pfizer (PFE) to Acquire Global Blood Therapeutics (GBT) for $5.4 Billion, $68.50 Per Share

