US researchers have led a study to examine a potential new treatment option for patients with nonalcoholic steatohepatitis (NASH)-related fibrosis. The results describe a drug, called Pegozafermin that mimics a hormone in the body and improves both liver fibrosis, and scarring of the liver, and liver inflammation in patients with NASH.


Identifying this drug for NASH is extremely promising for patients as currently there are no FDA-approved therapies for the condition. NASH can adversely impact the quality of life in patients and can progress to cirrhosis. Its complications can lead to death or liver transplantation.” Our findings will further the science of this disease and provide a potential new treatment option to those affected by NASH-related fibrosis,” an expert said.

The researchers said Pegozafermin mimicked fibroblast growth factor 21 (FGF21) — a liver-secreted peptide hormone that is naturally produced in the body. FGF21 controls energy use in the body and lipid metabolism in the liver. It has also been shown in previous studies to lower blood glucose and insulin levels, reducing body weight and liver fat.

The study’s results show that the new potential treatment not only improves fibrosis but also improves inflammation and liver injury along with significant improvements across multiple non-invasive biomarkers of NASH activity and scarring.

The 24-week, randomised clinical trial involved 222 participants with NASH assigned to either receive the drug or a placebo. Of the patients who received the drug at a higher dose, approximately 27 per cent showed an improvement in liver fibrosis, relative to 7 per cent of the patients who received the placebo. The most frequently reported side effects from the drug were gastrointestinal in nature, including nausea.

The next steps for this research will be a larger, multi-center, international trial with a more diverse patient population and longer treatment period to better assess the safety of the drug.
“If successfully shown to be both safe and effective in a larger Phase 3 trial, this drug could be used to treat millions of patients with NASH,” the researcher noted. IANS