Global Medical Affairs, Sanofi Pasteur, Swiftwater, PA.
Finnish Institute for Health and Welfare, Tampere, Finland.
Am Heart J. 2021 Jul;237:54-61. doi: 10.1016/j.ahj.2021.03.007. Epub 2021 Mar 13.
Influenza has been an acknowledged cause of respiratory disease for decades. However, considerable related, and often unappreciated, disease burden stems from cardiovascular complications, exacerbations of underlying medical conditions and secondary respiratory complications, with the highest burden in the elderly. This novel study combines the gold standard method of a randomized controlled trial with real-world data collection through national registries, to assess the relative effectiveness of high-dose (QIV-HD) vs standard-dose quadrivalent influenza vaccine (QIV-SD) in preventing cardio-respiratory hospitalizations in a large cohort of adults aged ≥65 years.
This trial (NCT04137887) is a Phase III/IV, modified double-blinded, randomized, registry-based trial, conducted by the Finnish Institute for Health and Welfare (THL). Participants (n>120 000) are being enrolled over multiple influenza seasons and randomized (1:1) to receive QIV-HD or QIV-SD. Participant follow-up is based on data collection up to 11 months post-vaccination using Finnish national health registries. The primary objective is to demonstrate the relative superior effectiveness of QIV-HD over QIV-SD in preventing cardio-respiratory hospitalizations up to 6 months post-vaccination. Safety will be assessed using automated online tools throughout the study, with causality assessed using statistical and probabilistic methods; serious adverse reactions and adverse events of special interest will be investigated individually.
This large, real-world, randomized study will provide valuable insight into the contribution of influenza in causing severe cardio-respiratory events, and the role of vaccination with QIV-HD in reducing these outcomes compared to the current standard of care.
Sanofi Pasteur.
几十年来,流感一直被认为是呼吸道疾病的一个公认病因。然而,相当多的相关疾病(通常未被认识到)负担源自心血管并发症、基础疾病恶化和继发性呼吸道并发症,在老年人中负担最高。这项新的研究将随机对照试验的金标准方法与通过国家登记处进行的真实世界数据收集相结合,以评估高剂量(QIV-HD)与标准剂量四价流感疫苗(QIV-SD)在预防≥65 岁的大量成年人中发生心肺住院的相对有效性。
这项试验(NCT04137887)是一项 III/IV 期、改良的双盲、随机、基于登记的试验,由芬兰卫生与福利研究所(THL)进行。参与者(n>120000)在多个流感季节被纳入,并以 1:1 的比例随机分配接受 QIV-HD 或 QIV-SD。使用芬兰国家卫生登记处,根据接种疫苗后长达 11 个月的数据收集对参与者进行随访。主要目的是证明 QIV-HD 在预防接种后 6 个月内发生心肺住院方面的相对优越性,优于 QIV-SD。通过整个研究期间使用自动在线工具评估安全性,并使用统计和概率方法评估因果关系;将单独调查严重不良反应和特别关注的不良事件。
这项大型真实世界的随机研究将为流感导致严重心肺事件的原因提供有价值的见解,并为使用 QIV-HD 疫苗接种相对于当前标准护理降低这些结果的作用提供有价值的见解。
赛诺菲巴斯德。