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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

Ginkgo Bioworks and SaponiQx Awarded MCDC Contract to Discover and Manufacture Next-Generation Vaccine Adjuvants Using Generative Molecular Design

BOSTON and LEXINGTON, Mass., Feb. 15, 2024 /PRNewswire/ The Defense Threat Reduction Agency s Joint Science and Technology Office for the Chemical and Biological Defense Program has awarded,.

United statesRebecca kurnatJennifer wipfAdjuvant developmentSaponiqx incDefense consortiumDefense threat reduction agencyExchange commissionGinkgo bioworks incTechnology officeAgenus incJoint scienceBiological defenseVaccines prototypeGinkgo bioworksGenerative molecular design

GSK s RSV Vaccine, AREXVY, Accepted Under Priority Review in US for the Prevention of RSV Disease in Adults Aged 50-59 at Increased Risk -February 06, 2024 at 07:04 am EST

Application supported by positive results of a phase III trial showing immune response and acceptable tolerability profile in this population Adults aged 50 and above with underlying medical.

United kingdomUnited kingdom generalJ clin virolRichard osei yeboahSaponiqx incCenters for diseaseAgenus incAntigenics incDrug administrationPriority reviewRespiratory syncytial virus vaccinePriority review voucherBiologics license applicationPrescription drug user fee actSyncytial virus vaccineSafety information

GSK s (GSK) RSV Vaccine, AREXVY, Accepted Under Priority Review in US

GSK s (GSK) RSV Vaccine, AREXVY, Accepted Under Priority Review in US
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United kingdomDrug administrationAntigenics incAgenus incSaponiqx incPriority reviewRespiratory syncytial virus vaccinePriority review voucherBiologics license applicationPrescription drug user fee actSyncytial virus vaccineSafety information