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Espervita's EVT0185 Demonstrates Reversal of Metabolic Dysfunction and Liver Fibrosis in Cell Metabolism Publication
EVT0185 reverses liver fibrosis by 38% and improves insulin sensitivity by targeting metabolic pathways in hepatic stellate cells and hepatocytes, addressing MASH drivers.
- On Jan. 6, 2026 in Ann Arbor, Mich., Espervita Therapeutics announced a Cell Metabolism publication showing EVT0185, a first-in-class dual ACLY/ACSS2 inhibitor, resolves MASH and liver fibrosis while lowering blood glucose and cholesterol.
- Obesity and type 2 diabetes affect hundreds of millions and drive MASH, now the fastest-growing cause of advanced liver disease, liver cancer and transplantation, creating an unmet need for fibrosis-reversing therapies.
- Preclinical studies demonstrated 38% reversal of hepatic fibrosis with direct inhibition of HSCs, alongside improved insulin sensitivity and reduced steatosis and inflammation without increased plasma triglycerides.
- Together, preclinical and prior tumor data imply efficacy in human liver slices and primary human HSCs supports clinical translatability, with potential to address downstream complications.
- Mechanistically, EVT0185 reprograms cytosolic acetyl-CoA metabolism in HSCs and hepatocytes by inhibiting ACLY and ACSS2, targeting metabolic drivers of fibrosis and systemic dysfunction.
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Espervita's EVT0185 Demonstrates Reversal of Metabolic Dysfunction and Liver Fibrosis in Cell Metabolism Publication
ANN ARBOR, Mich., Jan. 6, 2026 /PRNewswire/ -- Espervita Therapeutics, a biotechnology company developing targeted metabolic reprogramming therapies, announced the publication in Cell Metabolism of groundbreaking preclinical data demonstrating that its lead compound, EVT0185, a first-in-class dual inhibitor of ATP…
·Flint, United States
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