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基于ClinicalTrials.gov数据库分析非酒精性脂肪性肝炎干预性临床试验注册情况。

Analyzing MASLD interventional clinical trial registration based on the ClinicalTrials.gov database.

作者信息

Du Hui, Huang Jihan, Wang Youhua, Wang Chunyan, Wang Yiqun, Hou Luming, Li Yali, Li Ying, Su Qianmin

机构信息

Department of Infectious, Longhua Hospital, Affiliated to Shanghai University of Traditional Chinese Medicine, #725 Wanping South Road, Xuhui District, Shanghai, 200032, People's Republic of China.

Center for Drug Clinical Research, Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.

出版信息

BMC Gastroenterol. 2025 Mar 7;25(1):148. doi: 10.1186/s12876-025-03732-2.

Abstract

OBJECTIVE

With the rising incidence of MASLD, extensive drug research has been conducted in clinical trials. The study examined the design principles and research objectives of MASLD therapeutics, in order to offer guidance to clinical trial participants and decision makers.

METHODS

By searching the clinical research trial data registered on clinicaltrials.gov platform, 1209 interventional clinical trials were screened. These trials were subsequently evaluated based on clinical stage, trial design, intervention modalities, outcome metrics, and other pertinent factors.

RESULTS

A total of 1,209 trials were included, of which 199 were registered from 2000 to 2012 (16.46%) and 1010 were registered from 2013 to 2024 (83.54%), reflecting the growing body of research on MASLD. Regarding the intervention model type, single-group designs were employed in 232 (19.19%) trials, and parallel designs were employed in 873(72.21%). A total of 13 trials were early phase 1 (1.08%), 152 (12.57%) were phase 1, 34 (2.81%) were phase 1/phase 2, 301 were phase 2 (24.90%), 19 (1.57%) were phase 2/phase 3, 72 (5.96%) were phase 3, and 84 (6.95%) were phase 4. Within these trials, the three primary clinical outcomes for drug interventions were hepatic histological improvement, hepatic fat content and adverse events. Furthermore, 140 drug interventional trials with results for therapeutic purposes (This accounted for 88.61% of the 158 drug interventional trials with results) primarily aimed to improve MASLD through mechanisms such as metabolic and energy balance, inflammatory and immunomodulatory, and lipid reduction, targeting primarily PPAR, FXR, ACC and GLP-1.

CONCLUSION

This study suggests the basic characteristics of global MASLD clinical trial design, and the current global interventional clinical trials are mainly focused on drug-related treatments, and drugs to improve inflammation and metabolism are still the first choice for MASLD drug intervention studies.

摘要

目的

随着代谢相关脂肪性肝病(MASLD)发病率的上升,已在临床试验中开展了广泛的药物研究。本研究考察了MASLD治疗药物的设计原则和研究目标,以便为临床试验参与者和决策者提供指导。

方法

通过检索clinicaltrials.gov平台上注册的临床研究试验数据,筛选出1209项干预性临床试验。随后根据临床阶段、试验设计、干预方式、结局指标及其他相关因素对这些试验进行评估。

结果

共纳入1209项试验,其中199项于2000年至2012年注册(16.46%),1010项于2013年至2024年注册(83.54%),这反映出对MASLD的研究在不断增加。关于干预模型类型,232项(19.19%)试验采用单组设计,873项(72.21%)试验采用平行设计。共有13项为1期早期试验(1.08%),152项(12.57%)为1期试验,34项(2.81%)为1/2期试验,301项为2期试验(24.90%),19项(1.57%)为2/3期试验,72项(5.96%)为3期试验,84项(6.95%)为4期试验。在这些试验中,药物干预的三个主要临床结局为肝脏组织学改善、肝脏脂肪含量和不良事件。此外,140项有治疗结果的药物干预试验(占158项有结果的药物干预试验的88.61%)主要旨在通过代谢和能量平衡、炎症和免疫调节以及降脂等机制改善MASLD,主要靶点为过氧化物酶体增殖物激活受体(PPAR)、法尼醇X受体(FXR)、乙酰辅酶A羧化酶(ACC)和胰高血糖素样肽-1(GLP-1)。

结论

本研究揭示了全球MASLD临床试验设计的基本特征,当前全球干预性临床试验主要聚焦于药物相关治疗,改善炎症和代谢的药物仍是MASLD药物干预研究的首选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc1/11887356/46bcbbe178a9/12876_2025_3732_Fig1_HTML.jpg

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