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Biohaven and Pfizer Complete Collaboration Transaction for Commercialization of Rimegepant and Zavegepant Outside United States
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Pfizer (PFE) and BioNTech (BNTX) Sign New Global Collaboration Agreement to Develop First mRNA-based Shingles Vaccine
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Pfizer and BioNTech Sign New Global Collaboration Agreement to Develop First mRNA-based Shingles Vaccine
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Pfizer and BioNTech Sign New Global Collaboration Agreement to Develop First mRNA-based Shingles Vaccine
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Pfizer to supply U.S. with 10 million more courses of COVID-19 pills
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Pfizer (PFE) Says U.S. to Purchase an Additional 10 Million Courses of PAXLOVID
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Pfizer to Provide U.S. Government with an Additional 10 Million Treatment Courses of its Oral Therapy to Help Combat COVID-19
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Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer (PFE), BioNTech (BNTX) Confirm U.S. FDA Emergency Use Authorization of COVID-19 Vaccine Booster for Individuals 12 Years of Age and Older
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Pfizer and BioNTech Receive U.S. FDA Emergency Use Authorization of COVID-19 Vaccine Booster for Individuals 12 Years of Age and Older
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Pfizer Invites Public to Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer Invites Public to View and Listen to Webcast of February 8 Conference Call with Analysts
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Pfizer (PFE) Announces U.S. FDA Emergency Use Authorization for Novel COVID-19 Oral Antiviral Treatment
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Pfizer Receives U.S. FDA Emergency Use Authorization for Novel COVID-19 Oral Antiviral Treatment
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Pfizer (PFE) Announces Additional Order for 2.5M Courses of Oral Antiviral COVID-19 Candidate from the UK Government
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Pfizer to Provide the United Kingdom an Additional 2.5 Million Treatment Courses of Investigational Oral Antiviral Candidate to Help Combat COVID-19
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Pfizer's (PFE) VYNDAQEL/VYNDAMAX Reduced Risk of All-Cause Mortality by 41% Among Patients with Transthyretin Amyloid Cardiomyopathy, Five-Year Follow-Up Data Demonstrate
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Pfizer’s VYNDAQEL®/VYNDAMAX® Reduced the Risk of All-Cause Mortality by 41% Among Patients with Transthyretin Amyloid Cardiomyopathy, Five-Year Follow-Up Data Demonstrate
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Pfizer and BioNTech to Provide European Union More Than 200 Million Additional Doses of COMIRNATY® to Help Meet Continued Need for Vaccine Supply
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'Tidal wave': Omicron could put U.S. COVID-19 surge into overdrive
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EMA Issues Advice for Potential Early Use of Pfizer’s Novel COVID-19 Oral Antiviral Candidate
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Pfizer (PFE) Announces FDA Approval of XELJANZ for the Treatment of Active Ankylosing Spondylitis
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U.S. FDA Approves Pfizer’s XELJANZ® (tofacitinib) for the Treatment of Active Ankylosing Spondylitis
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Pfizer (PFE) says antiviral for covid significantly reduced risk of hospitalization or death
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Pfizer Announces Additional Phase 2/3 Study Results Confirming Robust Efficacy of Novel COVID-19 Oral Antiviral Treatment Candidate in Reducing Risk of Hospitalization or Death
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Pfizer to Acquire Arena Pharmaceuticals
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Sangamo Therapeutics (SGMO) and Pfizer (PFE) Announce Updated Phase 1/2 Results Showing Sustained Bleeding Control in Highest Dose Cohort Through Two Years Following Hemophilia A Gene Therapy
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Pfizer and Sangamo Announce Updated Phase 1/2 Results Showing Sustained Bleeding Control in Highest Dose Cohort Through Two Years Following Hemophilia A Gene Therapy
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Pfizer Declares First-Quarter 2022 Dividend
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Pfizer's (PFE) Cibinqo Approved in EU for Treatment of Adults with Moderate-to-Severe Atopic Dermatitis
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European Commission Approves Pfizer’s Cibinqo® (abrocitinib) for the Treatment of Adults with Moderate-to-Severe Atopic Dermatitis
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Arvinas Inc. (ARVN) and Pfizer (PFE) Announce PROTAC Protein Degrader ARV-471 Continues to Demonstrate Encouraging Clinical Benefit Rate in Patients with Locally Advanced or Metastatic ER+/HER2- Breas
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Arvinas and Pfizer Announce PROTAC® Protein Degrader ARV-471 Continues to Demonstrate Encouraging Clinical Benefit Rate in Patients with Locally Advanced or Metastatic ER+/HER2- Breast Cancer
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Arvinas and Pfizer Announce PROTAC® Protein Degrader ARV-471 Continues to Demonstrate Encouraging Clinical Benefit Rate in Patients with Locally Advanced or Metastatic ER+/HER2- Breast Cancer
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Pfizer and BioNTech Receive U.S. FDA Emergency Use Authorization of COVID-19 Vaccine Booster for Individuals 16 Years and Older
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Pfizer (PFE), BioNTech (BNTX) Confirm U.S. FDA Emergency Use Authorization of COVID-19 Vaccine Booster for Individuals 16 Years and Older
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Pfizer and BioNTech Receive U.S. FDA Emergency Use Authorization of COVID-19 Vaccine Booster for Individuals 16 Years and Older
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Pfizer and BioNTech Provide Update on Omicron Variant
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Pfizer (PFE) and BioNtech (BNTX) Announces Study Shows Omicron Variant is Neutralized by Their COVID-19 Vaccine With Three Doses
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Pfizer and BioNTech Provide Update on Omicron Variant
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Studies suggest Pfizer shot may protect only partially against Omicron
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Pfizer Invites Public to Register for Webcast of Analyst and Investor Call to Discuss Pfizer-BioNTech COVID-19 Vaccine and Pfizer’s Novel COVID-19 Oral Antiviral Treatment Candidate
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Forty Years on From the Start of the HIV Epidemic, New Data Reveals People Living With HIV Face Outdated Attitudes and Ongoing Discrimination
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Ionis Pharmaceuticals (IONS) Report Positive Topline Results from Pfizer's (PFE) Phase 2b Study of Vupanorsen
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Pfizer (PFE), BioNTech (BNTX) Follow-Up Data From Phase 3 Trial of COVID-19 Vaccine Support Safety and High Efficacy in Adolescents 12 Through 15 Years of Age
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BioNTech SE (BNTX) and Pfizer (PFE) Vaccine 100% Effectice Against COVID-19 in 12-15 Age Group per Phase 3 Study
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Follow-Up Data from Phase 3 Trial Of Pfizer-BioNTech COVID-19 Vaccine Support Safety and High Efficacy in Adolescents 12 Through 15 Years of Age
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Follow-Up Data From Phase 3 Trial of Pfizer-BioNTech COVID-19 Vaccine Support Safety and High Efficacy in Adolescents 12 Through 15 Years of Age
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Arvinas Inc. (ARVN), Pfizer (PFE) Announce Updated Phase 1 Dose Escalation Data for ARV-471 to be Presented in Spotlight Poster Session at 2021 San Antonio Breast Cancer Symposium

