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Investegate |AstraZeneca PLC Announcements | AstraZeneca PLC: Nirsevimab recommended for approval in EU by CHMP

Investegate announcements from AstraZeneca PLC, Nirsevimab recommended for approval in EU by CHMP

United statesUnited kingdomSanofi beyfortusAdrian kempIskra reicGlobal head of researchCalifornia perinatal associationEuropean unionBurden of communityJapan agency for medical researchCommittee for medicinal products human useCenters for diseaseEuropean medicines authorityDrug administrationEuropean commissionInvestor relations team

Press Release: CHMP recommends approval of Beyfortus® (nirsevimab) for prevention of RSV disease in infants

Press Release: CHMP recommends approval of Beyfortus® (nirsevimab) for prevention of RSV disease in infants
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United statesFrance generalUnited kingdomNicolas obristCorentine driancourtRelationssandrine guendoulFelix lauscherRelationseva schaefer jansenKate conwayNathalie phamSally bainPriya nanduriCenters for diseaseToussaintglobal head of researchDrug administrationRegulatory agency

Advancing the Science of RSV

Advancing the Science of RSV
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United statesVan barneveldCenters for diseaseDecades of researchA partnershipInfectious diseases societyBurden of communityRespiratory syncytial virusFor sannePartnership dedicatedSyncytial virusDisease controlAccessed maySyncytial virus infectionAssociated hospitalizationsYoung children

Pfizer Granted FDA Breakthrough Therapy Designation for Respiratory Syncytial Virus Vaccine Candidate for the Prevention of RSV in Older Adults

Pfizer Inc. today announced that its respiratory syncytial virus vaccine candidate, PF-06928316 or RSVpreF, received Breakthrough Therapy Designation from the U.S. Food and Drug Administration for. | March 24, 2022

United statesKathrinu jansenCenters for diseaseNational institutes of healthDrug administrationExchange commissionPfizer incBreakthrough therapy designationSenior vice presidentVaccine researchTherapy designationNational institutesFast trackBreakthroughs that change patientPfizer newsAnnual report

Pfizer Announces Start of Phase 3 Clinical Trial in Adults for Its Investigational Vaccine Against Respiratory Syncytial Virus (RSV)

Pfizer Announces Start of Phase 3 Clinical Trial in Adults for Its Investigational Vaccine Against Respiratory Syncytial Virus (RSV)
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Bryan dunnKathrinu jansenSteve danehyExchange commissionCenters for diseasePfizer incNational institutes of healthSenior vice presidentVaccine researchNational institutesFast trackBreakthroughs that change patientPfizer newsAnnual reportLooking informationFactors that may affect future