A revisit of drugs and potential therapeutic targets against non-alcoholic fatty liver disease: learning from clinical trials

被引:6
作者
Zhu, S. [1 ]
Wu, Z. [1 ]
Wang, W. [1 ]
Wei, L. [2 ]
Zhou, H. [2 ]
机构
[1] Jiangnan Univ, Wuxi Sch Med, Wuxi, Peoples R China
[2] Anhui Med Univ, Sch Life Sci, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-alcoholic fatty liver disease; Clinical trial; Drug; Therapeutic target; INSULIN-RESISTANCE; TREATMENT-OPTIONS; RECEPTOR AGONIST; OBETICHOLIC ACID; DUAL GIP; STEATOHEPATITIS; FIBROSIS; OBESITY; METABOLISM; PLACEBO;
D O I
10.1007/s40618-023-02216-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PurposeNon-alcoholic fatty liver disease (NAFLD) is the most common liver disease, with a worldwide prevalence of 25%. Although numerous clinical trials have been conducted over the last few decades, an effective treatment has not been approved yet. Extensive research has accumulated a large amount of data and experience; however, the vast number of clinical trials and new therapeutic targets for NAFLD make it impossible to keep abreast of the relevant information. Therefore, a systematic analysis of the existing trials is necessary.MethodsHere, we reviewed clinical trials on NAFLD registered in the mandated federal database, ClinicalTrials.gov, to generate a detailed overview of the trials related to drugs and therapeutic targets for NAFLD treatment. Following screening for pertinence to therapy, a total of 440 entries were identified that included active trials as well as those that have already been completed, suspended, terminated, or withdrawn.ResultsWe summarize and systematically analyze the state, drug development pipeline, and discovery of treatment targets for NAFLD. We consider possible factors that may affect clinical outcomes. Furthermore, we discussed these results to explore the mechanisms responsible for clinical outcomes.ConclusionWe summarised the landscape of current clinical trials and suggested the directions for future NAFLD therapy to assist internal medicine specialists in treating the whole clinical spectrum of this highly prevalent liver disease.
引用
收藏
页码:761 / 776
页数:16
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