Proal Amy D, Aleman Soo, Bomsel Morgane, Brodin Petter, Buggert Marcus, Cherry Sara, Chertow Daniel S, Davies Helen E, Dupont Christopher L, Deeks Steven G, Ely E Wes, Fasano Alessio, Freire Marcelo, Geng Linda N, Griffin Diane E, Henrich Timothy J, Hewitt Stephen M, Iwasaki Akiko, Krumholz Harlan M, Locci Michela, Marconi Vincent C, Mehandru Saurabh, Muller-Trutwin Michaela, Painter Mark M, Pretorius Etheresia, Price David A, Putrino David, Qian Yu, Roan Nadia R, Salmon Dominique, Tan Gene S, VanElzakker Michael B, Wherry E John, Van Weyenbergh Johan, Yonker Lael M, Peluso Michael J
PolyBio Research Foundation, Medford, MA, USA.
Department of Infectious Diseases and Unit of Post-COVID Huddinge, Karolinska University Hospital, Stockholm, Sweden; Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Lancet Infect Dis. 2025 May;25(5):e294-e306. doi: 10.1016/S1473-3099(24)00769-2. Epub 2025 Feb 10.
There are no approved treatments for post-COVID-19 condition (also known as long COVID), a debilitating disease state following SARS-CoV-2 infection that is estimated to affect tens of millions of people. A growing body of evidence shows that SARS-CoV-2 can persist for months or years following COVID-19 in a subset of individuals, with this reservoir potentially driving long-COVID symptoms or sequelae. There is, therefore, an urgent need for clinical trials targeting persistent SARS-CoV-2, and several trials of antivirals or monoclonal antibodies for long COVID are underway. However, because mechanisms of SARS-CoV-2 persistence are not yet fully understood, such studies require important considerations related to the mechanism of action of candidate therapeutics, participant selection, duration of treatment, standardisation of reservoir-associated biomarkers and measurables, optimal outcome assessments, and potential combination approaches. In addition, patient subgroups might respond to some interventions or combinations of interventions, making post-hoc analyses crucial. Here, we outline these and other key considerations, with the goal of informing the design, implementation, and interpretation of trials in this rapidly growing field. Our recommendations are informed by knowledge gained from trials targeting the HIV reservoir, hepatitis C, and other RNA viruses, as well as precision oncology, which share many of the same hurdles facing long-COVID trials.
新冠后状况(也称为长期新冠)是指感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)后出现的一种使人衰弱的疾病状态,估计有数千万人受其影响,目前尚无获批的治疗方法。越来越多的证据表明,在一部分个体中,SARS-CoV-2在新冠后可持续存在数月或数年,这种病毒库可能导致长期新冠症状或后遗症。因此,迫切需要针对持续存在的SARS-CoV-2进行临床试验,目前正在进行几项针对长期新冠的抗病毒药物或单克隆抗体试验。然而,由于SARS-CoV-2持续存在的机制尚未完全了解,此类研究需要对候选治疗药物的作用机制、参与者选择、治疗持续时间、与病毒库相关的生物标志物和可测量指标的标准化、最佳结局评估以及潜在的联合治疗方法等进行重要考量。此外,患者亚组可能对某些干预措施或干预措施组合有反应,这使得事后分析至关重要。在此,我们概述这些及其他关键考量因素,目的是为这个快速发展领域的试验设计、实施和解读提供参考。我们的建议借鉴了针对艾滋病毒病毒库、丙型肝炎和其他RNA病毒的试验以及精准肿瘤学所获得的知识,这些领域与长期新冠试验面临许多相同的障碍。