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. 2024 Jul 6;14:90. doi: 10.1186/s13578-024-01267-9

Table 1.

Drug candidates for MASH

Drug target Drug name Mechanism of action Side effect Trial number
PPAR agonist Pioglitazone Enhances insulin sensitivity by activating PPARγ Weight gain and bone loss NCT00994682
Saroglitazar Improves insulin resistance and modulating gluconeogenesis, β-oxidation by activating PPARα/γ Almost no adverse drug reactions NCT03061721
SGLT-2 inhibitor Empagliflozin Downregulates renal glucose threshold and enhances urinary excretion of glucose to reduce hyperglycemia by inhibiting SGLT2 Ketoacidosis NCT02686476
Obeticholic acid NCT02548351
FXR agonist EDP-305 Improves insulin sensitivity and reduces the expression of markers of liver fibrosis and inflammation by activating FXR High risk of long-term cardiovascular diseases NCT03421431
THRβ agonist Resmetirom Modulates hepatic lipid metabolism by acting on THR; Restores RGS5 expression and inhibits STAT3 and NF-κB signaling pathway Transient mild diarrhea and nausea NCT03900429
SCD1 inhibitor Aramchol Controls hepatic steatosis by inhibiting SCD1, a central regulator of fuel metabolism No serious adverse drug reactions NCT02279524
Ketohexokinase inhibitor PF-06835919 Inhibits ketohexokinase, the critical enzyme involved in fructose metabolism No serious adverse events NCT03256526
Fibroblast growth factor 19 NGM282 Increase metabolic rate and reduce adiposity Increase the risk of cardiovascular disease NCT02443116
Fibroblast growth factor 21 Pegozafermin Regulates energy balance, glucose, and lipid homeostasis by acting on FGF21 receptor Diarrhoea and nausea NCT04929483