Research, Lupus Foundation of America, Washington, District of Columbia, USA
Health Policy and Regulatory Affairs, Faegre Drinker Biddle and Reath LLP Washington, Washington, District of Columbia, USA.
Lupus Sci Med. 2023 Feb;10(1). doi: 10.1136/lupus-2023-000901. Epub 2023 Feb 14.
Drug development in lupus has improved over the past 10 years but still lags behind that of other rheumatic disease areas. Assessment of prospective lupus therapies in clinical trials has proved challenging for reasons that are multifactorial including the heterogeneity of the disease, study design limitations and a lack of validated biomarkers which greatly impacts regulatory decision-making. Moreover, most composite outcome measures currently used in trials do not include patient-reported outcomes. Given these factors, the Addressing Lupus Pillars for Health Advancement Global Advisory Committee members who serve on the drug development team identified an opportunity to convene a meeting to facilitate information sharing on completed and existing outcome measure development efforts. This meeting report highlights information presented during the meeting as well as a discussion on how the lupus community may work together with regulatory agencies to simplify and standardise outcome measures to accelerate development of lupus therapeutics.
过去 10 年来,狼疮的药物研发取得了进展,但仍落后于其他风湿性疾病领域。临床试验中对潜在狼疮治疗方法的评估具有挑战性,原因是多方面的,包括疾病的异质性、研究设计的局限性以及缺乏经过验证的生物标志物,这极大地影响了监管决策。此外,目前临床试验中使用的大多数综合结局指标都不包括患者报告的结局。鉴于这些因素,药物研发团队中的狼疮领域全球顾问委员会成员认为有机会召开一次会议,以促进信息共享,了解已完成和正在进行的结局指标开发工作。本会议报告重点介绍了会议期间介绍的信息,并讨论了狼疮社区如何与监管机构合作,简化和标准化结局指标,以加速狼疮治疗药物的研发。