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. Author manuscript; available in PMC: 2017 Apr 23.
Published in final edited form as: Semin Liver Dis. 2015 Sep 17;35(3):338–348. doi: 10.1055/s-0035-1562951

Table 1.

Emerging therapeutic agents for NASH

Agent Putative mechanism/s Effects on NAFLD Studies in human NAFLD
Obeticholic acid FXR ligand Improves glucose and lipid metabolism Improves histology including fibrosis Yes
Fibroblast growth factor 21 Regulates glucose and lipid metabolism Improves histology in animal models including fibrosis Not known
Exenatide and Liraglutide GLP-1 agonist Regulates glucose metabolism and post-prandial insulin sectretion Improves histology including fibrosis Yes. Recently presented liraglutide data offer exciting results.
Cysteamine Bitartrate glutathione precursor Antioxidant Improves ALT and keratin-18 Yes, Ongoing clinical trial
Simtuzumab LOXL2 antagonist Antifibrotic Unknown Yes, Ongoing clinical trial
GR-MD-02 galactin 3 inhibitor Improves fibrosis in murine models Yes, Ongoing clinical trial
Cenicriviroc inhibitor of CCR 2 and 5 Improves hepatic inflammation and fibrosis on murine models Yes, Ongoing clinical trial
Aramchol fatty acid–bile acid conjugate Inhibits stearoyl coenzyme A desaturase 1 Decreased hepatic fat content Yes, Ongoing clinical trial
GFT505 PPAR α and δ agonist Imporves insulin sensitivity and lipid metabolism Improves hepatic steatosis, inflammation and fibrosis in murine models Yes, the scientific results of the GOLDEN 505 trial are awaited