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Specific research results show that, at the time of testing during the second epidemic season,AbrysvoThe efficacy of preventing RSV-related lower respiratory tract diseases (with three or more symptoms) is 77.8%; the vaccine's protective efficacy after the first epidemic season is 88.9%, indicatingAbrySVO still has lasting protective efficacy after two epidemic seasons.
After the second epidemic season,AbrySVO for three or more symptomsRSV A and B typesPreventionConsistent efficacy, both ≥80%.In the case of two or more mild symptomsofLower Respiratory Tract DiseasesThePreventive EfficacyIs also ongoing,ByThe First Season65.1%After the end of Season 255.7%。
Moreover, after approximately 16.4 months of monitoring,AbrySVO for RSV-The protective efficacy of LRTD (three or more symptoms) was 81.5%. No new adverse event reports were observed in the study.
AbrySVO was approved by the FDA for use in people aged 60 and above by the end of May 2023, and three months later received another FDA approval to expand its indications, providing vaccination for pregnant women to protect newborns. Although in its first year on the market,AbrySVO generated $890 million in sales, but lagged behind the product fromGSKVaccineArexvySales (approximately 1.5 billion USD).
Besides, Pfizer'sAbrySVO will also cooperate withSanofi/AstraZenecaCo-developed RSV MonoclonalAnti-BeyfortusLaunch competition.Beyfortus was approved for marketing by the FDA in July 2023.Used to prevent lower respiratory tract diseases caused by respiratory syncytial virus in infants and young children, with last year's sales reaching 547 million euros (592 million US dollars).
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