Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Institute of Liver Studies, King's College Hospital NHS Foundation Trust, London, UK.
Trials. 2021 Nov 11;22(1):792. doi: 10.1186/s13063-021-05719-2.
Alcohol consumption causes a spectrum of liver abnormalities and leads to over 3 million deaths per year. Alcoholic hepatitis (AH) is a florid presentation of alcoholic liver disease characterized by liver failure in the context of recent and heavy alcohol consumption. The aim of this study is to explore the potential benefits of the IL-1β antibody, canakinumab, in the treatment of AH.
This is a multicentre, double-blind, randomised placebo-controlled trial. Participants will be diagnosed with AH using clinical criteria. Liver biopsy will then confirm that all histological features of AH are present. Up to 58 participants will be recruited into two groups from 15 centres in the UK. Patients will receive an infusion of Canakinumab or matched placebo by random 1:1 allocation. The primary outcome is the difference between groups in the proportion of patients demonstrating histological improvement and will compare histological appearances at baseline with appearances at 28 days to assign a category of "improved" or "not improved". Patients with evidence of ongoing disease activity will receive a second infusion of canakinumab or placebo. Participants will be followed up for 90 days. Secondary outcomes include mortality and change in MELD score at 90 days.
This phase II study will explore the benefits of the IL-1β antibody, canakinumab, in the treatment of AH to provide proof of concept that inhibition of IL-1β signalling may improve histology and survival for patients with AH.
EudraCT 2017-003724-79 . Prospectively registered on 13 April 2018.
饮酒会导致一系列的肝脏异常,并导致每年超过 300 万人死亡。酒精性肝炎(AH)是一种在近期和大量饮酒背景下发生的肝脏衰竭的急性酒精性肝病表现。本研究旨在探讨白细胞介素-1β(IL-1β)抗体卡那单抗治疗 AH 的潜在益处。
这是一项多中心、双盲、随机、安慰剂对照试验。参与者将根据临床标准诊断为 AH。肝活检将随后证实所有 AH 的组织学特征均存在。在英国的 15 个中心,最多将有 58 名患者被招募到两组中。患者将随机接受卡那单抗或匹配的安慰剂输注。主要结局是两组患者在组织学改善比例上的差异,将通过比较基线和 28 天的组织学表现来分配“改善”或“未改善”的类别。有持续疾病活动证据的患者将接受第二次卡那单抗或安慰剂输注。参与者将接受 90 天的随访。次要结局包括 90 天死亡率和 MELD 评分变化。
这项 2 期研究将探索白细胞介素-1β(IL-1β)抗体卡那单抗在治疗 AH 中的益处,为抑制 IL-1β 信号可能改善 AH 患者的组织学和生存率提供概念验证。
EudraCT 2017-003724-79 。2018 年 4 月 13 日前瞻性注册。