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GSK : DO NOT COURIER US FDA approves expanded age indication for GSK s Arexvy, the first respiratory syncytial virus (RSV) vaccine for adults aged 50-59 at increased risk

Over 13 million US adults aged 50-59 years have a medical condition that increases their risk of severe RSV outcomes1 Clinical development programme continues to.

United statesAnnr falseyTony woodConference on vaccinology researchSaponiqx incForum infectious diseasesUniversity of rochester school medicineDrug administrationCenters for diseaseNational foundation for infectious diseasesAntigenics incAgenus incRespiratory syncytial virusChief scientific officerRochester schoolSyncytial virus vaccine

US FDA Approves Expanded Age Indication for GSK s AREXVY, the First Respiratory Syncytial Virus (RSV) Vaccine for Adults Aged 50-59 at Increased Risk

Over 13 million US adults aged 50-59 years have a medical condition that increases their risk of severe RSV outcomes1 Clinical development program continues to evaluate safety and immunogenicity.

United statesTony woodAnnr falseyNational foundation for infectious diseasesDrug administrationUniversity of rochester school medicineCenters for diseaseAntigenics incConference on vaccinology researchSaponiqx incAgenus incForum infectious diseasesRespiratory syncytial virusBusiness wireChief scientific officerRochester school

Pfizer Announces Positive Top-Line Results from Phase 3 Study of ABRYSVO® in Adults Aged 18 to 59 at Increased Risk for RSV Disease

Pfizer Announces Positive Top-Line Results from Phase 3 Study of ABRYSVO® in Adults Aged 18 to 59 at Increased Risk for RSV Disease
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United statesAnnaliesa andersonFinkd immunobridgingAlimentosy tecnologForum infect disHealth canadaCenters for diseaseSurveillance researchWork group considerationsRegulatory agencyVaccine researchEuropean medicines agencyMinistry of healthPfizer incTherapeutic goods administration of australiaAdministration bureau of macau

Pfizer Announces Positive Top-Line Data for Full Season Two Efficacy of ABRYSVO® for RSV in Older Adults

ABRYSVO, a bivalent vaccine, maintained consistently high protective efficacy for both RSV A and RSV B disease through two seasons after a single dose. ABRYSVO efficacy was 77.8% against RSV.

United statesAlimentosy tecnologAnnaliesa andersonAdministration bureau of macauVaccine researchHealth canadaRegulatory agencyMinistry of healthCenters for diseaseForum infect disPfizer incExchange commissionSurveillance researchWork group considerationsEuropean medicines agencySouthern hemispheres

Pfizer Receives Positive FDA Advisory Committee Votes Supporting Potential Approval for Vaccine Candidate to Help Combat RSV in Older Adults

Pfizer Receives Positive FDA Advisory Committee Votes Supporting Potential Approval for Vaccine Candidate to Help Combat RSV in Older Adults
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United statesAnnaliesa andersonCenters for diseaseForum infect disNational institutes of healthDrug administrationExchange commissionPfizer incVaccine researchWork group considerationsSurveillance researchProducts advisory committeeRelated biological products advisory committeeSenior vice presidentChief scientific officerPrescription drug user fee act