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Press Release: Beyfortus real-world evidence published in The Lancet shows 82% reduction in infant RSV hospitalizations

Beyfortus real-world evidence published in The Lancet shows 82% reduction in infant RSV hospitalizations New real-world evidence shows Beyfortus substantially reduced RSV lower respiratory tract.

United kingdomFrance generalUnited statesComunidad autonoma de aragonSandrine guendoulFederico martinon torresThomas kudsk larsenSally bainEvan berlandNicolas obristTarik elgoutniFelix lauscherCorentine driancourtNathalie phamThomas triompheUs centers for disease

AstraZeneca Nirsevimab unanimously recommended by FDA Advisory Committee

AstraZeneca Nirsevimab unanimously recommended by FDA Advisory Committee

United kingdomUnited statesAnn roberth lurieThomas triompheBeyfortus nirsevimabWilliam mullerIskra reicNational medical products administrationCommunity trialsAntimicrobial drugs advisory committee meetingNorthwestern university feinberg school of medicineChina centerAlliance revenueCenters for diseaseLancet child adolesc healthEuropean medicines agency

Safety, tolerability, and immunogenicity of the respiratory syncytial virus prefusion F subunit vaccine DS-Cav1: a phase 1, randomised, open-label, dose-escalation clinical trial

Safety, tolerability, and immunogenicity of the respiratory syncytial virus prefusion F subunit vaccine DS-Cav1: a phase 1, randomised, open-label, dose-escalation clinical trial
thelancet.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thelancet.com Daily Mail and Mail on Sunday newspapers.

United statesVan kirkGonzalez lopezEnglj medInfect disIgab cellVaccine immunolDose nirsevimabOpin virolMed virolஒன்றுபட்டது மாநிலங்களில்வேன் கர்க்கோன்சலஸ் லோபஸ்தொற்று திஸ்மேட் வைரோல்

Sanofi: MHRA Grants Promising Innovative Medicine Designation to Nirsevimab

Sanofi: MHRA Grants Promising Innovative Medicine Designation to Nirsevimab 1,2 RSV is a contagious virus, and the most common cause of severe lower respiratory tract infections (LRTI) in infants and young children, resulting in over 30,000 hospitalisations per year in the UK due to RSV-associated LRTIs for children under five years 3 Promising Innovative Medicine (PIM) Designation was granted based on non-clinical and clinical data of nirsevimab in healthy preterm infants Nirsevimab does not have a Marketing Authorisation (MA) in the UK for any indication FOR MEDICAL AND PHARMACEUTICAL TRADE MEDIA ONLY The Medicines and Healthcare Products Regulatory Agency (MHRA) has granted a Promising Innovative Medicine (PIM) Designation to nirsevimab, an extended half-life monoclonal antibody (mAb) being investigated as a passive immunisation for the prevention of lower respiratory tract infections (LRTI) caused by respiratory syncytial virus (RSV) in all infants in their first RSV se

United kingdomSanofi pasteurIan grayAndrea welchDrug administrationLancet public healthVaccines communicationsEuropean medicines agencyOxford vaccines groupHealthcare products regulatory agencyVaccines immunizations centers for diseaseInnovative medicineMarketing authorisationPromising innovative medicineSanofi united kingdom medicalBreakthrough therapy designation