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FDA Approves Expanded Age Indication for Arexvy RSV Vaccine

The expanded indication is for the prevention of respiratory syncytial virus-associated lower respiratory tract disease in adults aged 50 through 59 years who are at an increased risk.

Tony woodAdvisory committee on immunization practicesUniversity of rochester school medicineImmunization practicesImmune responseVaccine against respiratory syncytial virus givenIncluding adultsIncreased riskOlder adultsRochester school

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

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Cayman: OfReg Board s Response to CUC s Press Release on Power Shedding

Cayman: OfReg Board s Response to CUC s Press Release on Power Shedding
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