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Articles published by Pfizer Inc.

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Pfizer’s Novel COVID-19 Oral Antiviral Treatment Candidate Reduced Risk of Hospitalization or Death by 89% in Interim Analysis of Phase 2/3 EPIC-HR Study
From Pfizer Inc.
Via Business Wire
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PFIZER REPORTS THIRD-QUARTER 2021 RESULTS
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Receive First U.S. FDA Emergency Use Authorization of a COVID-19 Vaccine in Children Ages 5 Through 11 Years
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech to Provide U.S. Government an Additional 50 Million Pediatric Doses of COVID-19 Vaccine to Support Further Preparedness for Future Needs
From Pfizer Inc.
Via Business Wire
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FDA Advisory Committee Votes in Favor of Granting Emergency Use Authorization for the Pfizer-BioNTech COVID-19 Vaccine in Children 5 to <12 Years
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Announce Phase 3 Trial Data Showing High Efficacy of a Booster Dose of Their COVID-19 Vaccine
From Pfizer Inc.
Via Business Wire
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Advisory Committee on Immunization Practices Votes to Recommend Routine Use of Pfizer’s PREVNAR 20™ (Pneumococcal 20-valent Conjugate Vaccine) in Adults
From Pfizer Inc.
Via Business Wire
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Pfizer’s Abrocitinib Receives Positive CHMP Opinion for the Treatment of Adults with Moderate to Severe Atopic Dermatitis
From Pfizer Inc.
Via Business Wire
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Japan’s MHLW Approves Pfizer’s CIBINQO® (abrocitinib) for Adults and Adolescents with Moderate to Severe Atopic Dermatitis
From Pfizer Inc.
Via Business Wire
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Positive Top-line Results of Pfizer’s Phase 3 Study Exploring Coadministration of Prevnar 20™ With Seasonal Flu Vaccine in Older Adults Released
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Submit Initial Data to U.S. FDA From Pivotal Trial of COVID-19 Vaccine in Children 5 to <12 Years of Age
From Pfizer Inc.
Via Business Wire
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Pfizer Starts Study of mRNA-Based Next Generation Flu Vaccine Program
From Pfizer Inc.
Via Business Wire
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Pfizer Starts Global Phase 2/3 EPIC-PEP Study of Novel COVID-19 Oral Antiviral Candidate for Post-Exposure Prophylaxis in Adults
From Pfizer Inc.
Via Business Wire
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Pfizer Invites Public to View and Listen to Webcast of Pfizer November 2 Conference Call with Analysts
From Pfizer Inc.
Via Business Wire
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Pfizer Declares Fourth-Quarter 2021 Dividend
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Receive First U.S. FDA Emergency Use Authorization of a COVID-19 Vaccine Booster
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Expand Collaboration with U.S. to Provide 500 Million Additional COVID-19 Vaccine Doses at Not-for-Profit Price for Donation to Poorest Countries
From Pfizer Inc.
Via Business Wire
Tickers BNTX PFE
Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Announce Positive Topline Results From Pivotal Trial of COVID-19 Vaccine in Children 5 to 11 Years
From Pfizer Inc.
Via Business Wire
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FDA Advisory Committee Votes Unanimously in Favor Of COMIRNATY® Booster for Emergency Use in People 65 and Older and Certain High-risk Populations
From Pfizer Inc.
Via Business Wire
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UK’s MHRA Grants Marketing Authorisation for Pfizer’s CIBINQO® (abrocitinib) for Adults and Adolescents With Moderate to Severe Atopic Dermatitis
From Pfizer Inc.
Via Business Wire
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Pfizer Invites Public to Listen to Two Webcasts of Pfizer Discussions at Upcoming Healthcare Conferences
From Pfizer Inc.
Via Business Wire
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Pfizer Announces Start of Phase 3 Clinical Trial in Adults for Its Investigational Vaccine Against Respiratory Syncytial Virus (RSV)
From Pfizer Inc.
Via Business Wire
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Positive Top-Line Results From Pfizer’s Phase 3 JADE DARE Trial Comparing the Efficacy of Abrocitinib and Dupilumab for Moderate to Severe Atopic Dermatitis
From Pfizer Inc.
Via Business Wire
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Pfizer Announces New Chief Business Innovation Officer
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Announce Collaboration With Brazil’s Eurofarma to Manufacture COVID-19 Vaccine Doses for Latin America
From Pfizer Inc.
Via Business Wire
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Pfizer and BioNTech Initiate Rolling Submission of Supplemental Biologics License Application to U.S. FDA for Booster Dose of COMIRNATY® in Individuals 16 and Older
From Pfizer Inc.
Via Business Wire
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Pfizer-BioNTech COVID-19 Vaccine COMIRNATY® Receives Full U.S. FDA Approval for Individuals 16 Years and Older
From Pfizer Inc.
Via Business Wire
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Pfizer to Acquire Trillium Therapeutics Inc.
From Pfizer Inc.
Via Business Wire
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XELJANZ® (tofacitinib citrate) Receives Marketing Authorization in the European Union for the Treatment of Active Polyarticular Juvenile Idiopathic Arthritis and Juvenile Psoriatic Arthritis
From Pfizer Inc.
Via Business Wire
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