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Pfizer to Acquire Global Blood Therapeutics for $5.4 Billion to Enhance Presence in Rare Hematology
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Pfizer to Acquire Global Blood Therapeutics for $5.4 Billion to Enhance Presence in Rare Hematology
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Myovant Sciences and Pfizer Receive U.S. FDA Approval of MYFEMBREE®, a Once-Daily Treatment for the Management of Moderate to Severe Pain Associated With Endometriosis
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Myovant Sciences and Pfizer Receive U.S. FDA Approval of MYFEMBREE®, a Once-Daily Treatment for the Management of Moderate to Severe Pain Associated With Endometriosis
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BioNTech SE (BNTX) and Pfizer (PFE) Advance COVID-19 Vaccine Strategy With Study Start of Next-Generation Vaccine Candidate Based on Enhanced Spike Protein Design
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Pfizer and BioNTech Advance COVID-19 Vaccine Strategy With Study Start of Next-Generation Vaccine Candidate Based on Enhanced Spike Protein Design
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Pfizer (PFE) Submits US NDA for PAXLOVID
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Pfizer Announces Submission of New Drug Application to the U.S. FDA for PAXLOVID™
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Pfizer (PFE), BioNTech (BNTX) Announce New Agreement with U.S. Government to Provide Additional Doses of COVID-19 Vaccine
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Pfizer and BioNTech Announce New Agreement with U.S. Government to Provide Additional Doses of COVID-19 Vaccine
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Pfizer and BioNTech Announce New Agreement with U.S. Government to Provide Additional Doses of COVID-19 Vaccine
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Roivant (ROIV) and Pfizer (PFE) Unveil Priovant Therapeutics and Ongoing Registrational Studies for Oral Brepocitinib in Dermatomyositis and Lupus
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Roivant and Pfizer Unveil Priovant Therapeutics and Ongoing Registrational Studies for Oral Brepocitinib in Dermatomyositis and Lupus
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Roivant and Pfizer Unveil Priovant Therapeutics and Ongoing Registrational Studies for Oral Brepocitinib in Dermatomyositis and Lupus
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Roivant and Pfizer Unveil Priovant Therapeutics and Ongoing Registrational Studies for Oral Brepocitinib in Dermatomyositis and Lupus
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BioNTech SE (BNTX) and Pfizer (PFE) Report Omicron-Adapted COVID-19 Vaccine Candidates Demonstrate High Immune Response Against
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Pfizer and BioNTech Announce Omicron-Adapted COVID-19 Vaccine Candidates Demonstrate High Immune Response Against Omicron
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Pfizer and BioNTech Announce Omicron-Adapted COVID-19 Vaccine Candidates Demonstrate High Immune Response Against Omicron
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Pfizer Invites Public to View and Listen to Webcast of July 28 Conference Call with Analysts
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Valneva and Pfizer Announce Closing of Equity Investment
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Pfizer Declares Third-Quarter 2022 Dividend
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Valneva SE (VALN), Pfizer (PFE) Enter Equity Subscription Agreement and Update Terms of Collaboration
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Valneva and Pfizer Enter into an Equity Subscription Agreement and Update Terms of Collaboration Agreement for Lyme Disease Vaccine Candidate VLA15
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Valneva and Pfizer Enter into an Equity Subscription Agreement and Update Terms of Collaboration Agreement for Lyme Disease Vaccine Candidate VLA15
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Pfizer (PFE) and BioNTech (BNTX) COVID-19 Vaccine Receives FDA Emergency Use Authorization for Children 6 Months through 4 Years of Age
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Pfizer-BioNTech COVID-19 Vaccine Receives FDA Emergency Use Authorization for Children 6 Months through 4 Years of Age
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Pfizer-BioNTech COVID-19 Vaccine Receives FDA Emergency Use Authorization for Children 6 Months through 4 Years of Age
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Myovant Sciences (MYOV) and Pfizer (PFE) Announce Publication of Phase 3 SPIRIT 1 and SPIRIT 2 Studies of Once-Daily Relugolix Combination Therapy in Women With Endometriosis-Associated Pain
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Myovant Sciences and Pfizer Announce Publication in The Lancet of Phase 3 SPIRIT 1 and SPIRIT 2 Studies of Once-Daily Relugolix Combination Therapy in Women With Endometriosis-Associated Pain
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Myovant Sciences and Pfizer Announce Publication in The Lancet of Phase 3 SPIRIT 1 and SPIRIT 2 Studies of Once-Daily Relugolix Combination Therapy in Women With Endometriosis-Associated Pain
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Pfizer (PFE) Reports Additional Data on PAXLOVID Supporting Upcoming NDA Submission to U.S. FDA
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Pfizer Reports Additional Data on PAXLOVID™ Supporting Upcoming New Drug Application Submission to U.S. FDA
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Pfizer (PFE), MorphoSys (MOR) and Incyte (INCY) Enter into Clinical Trial Collaboration for Monjuvi® (tafasitamab-cxix) in Combination with TTI-622, a Fusion Protein Directed Against CD47
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Pfizer, MorphoSys and Incyte Enter into Clinical Trial Collaboration for Monjuvi® (tafasitamab-cxix) in Combination with TTI-622, a Fusion Protein Directed Against CD47
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Pfizer (PFE) Completes Acquisition of ReViral
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Pfizer Completes Acquisition of ReViral
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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 Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer (PFE) to Invest $120 Million to Produce COVID-19 Oral Treatment in the U.S.
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Pfizer to Invest $120 Million to Produce COVID-19 Oral Treatment in the U.S.
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Pfizer (PFE) Reports Overall Survival Results from Phase 3 PALOMA-2 Trial of IBRANCE
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Pfizer Announces Overall Survival Results from Phase 3 PALOMA-2 Trial of IBRANCE® (palbociclib) for the First-Line Treatment of ER+, HER2- Metastatic Breast Cancer
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Myovant Sciences (MYOV), Pfizer (PFE) Announce FDA Acceptance of sNDA for MYFEMBREE®
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Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE®
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Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE®
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Pfizer Invites Public to View and Listen to a Webcast of Pfizer Discussion on Expanding Access & Affordability
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Pfizer (PFE) Granted FDA Fast Track Designation for Ervogastat/Clesacostat Combination
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Pfizer Granted FDA Fast Track Designation for Ervogastat/Clesacostat Combination for the Treatment of Non-Alcoholic Steatohepatitis (NASH)
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Pfizer Invites Public to View and Listen to Webcast of Pfizer Discussion at Healthcare Conference
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Pfizer Launches 'An Accord for a Healthier World' to Improve Health Equity for 1.2 Billion People Living in 45 Lower-Income Countries

