Workshop on the design and use of clinical trials with multiple endpoints, with a focus on prevention of RSV

IF 2.7 Q3 IMMUNOLOGY
O. Prunas , J. Willemsen , J.L. Warren , L. Bont , J.L. Schwartz , J. Atwell , E. Begier , N. Dean , I. Hirsch , R. Karron , K. Klugman , R. Kramer , E. Leidman , R. Link-Gelles , H. Nair , CA. Panozzo , E. Pelfrene , E.A.F. Simões , P.G. Smith , P. Srikantiah , D.M. Weinberger
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引用次数: 0

Abstract

A meeting held in Lisbon, Portugal, in February 2023 focused on critical aspects of clinical trial design for respiratory syncytial virus (RSV) preventative therapies. The meeting addressed two primary areas: enhancing the efficiency and success of randomized controlled trials (RCTs) for RSV preventative therapies and designing RCTs to better inform post-licensure decision-making. Topics included the selection of primary endpoints, innovative approaches to incorporating multiple endpoints and historical data, and the challenges and benefits of sequential trial designs. The discussion also touched on meta-regression models for obtaining more robust, context-specific estimates of vaccine efficacy. Overall, the meeting underscored the importance of balancing efficiency and robustness in RSV vaccine trial design, while recognizing the need for further discussions involving regulatory and advisory bodies.

关于设计和使用多终点临床试验的研讨会,重点是预防 RSV
2023 年 2 月在葡萄牙里斯本举行的一次会议重点讨论了呼吸道合胞病毒 (RSV) 预防性疗法临床试验设计的关键方面。会议讨论了两个主要领域:提高 RSV 预防性疗法随机对照试验 (RCT) 的效率和成功率,以及设计 RCT 以更好地为许可后决策提供信息。议题包括主要终点的选择、纳入多个终点和历史数据的创新方法以及顺序试验设计的挑战和益处。讨论还涉及元回归模型,以获得更可靠的、针对具体情况的疫苗疗效估计值。总之,会议强调了在 RSV 疫苗试验设计中平衡效率和稳健性的重要性,同时也认识到需要监管和咨询机构的进一步讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vaccine: X
Vaccine: X Multiple-
CiteScore
2.80
自引率
2.60%
发文量
102
审稿时长
13 weeks
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