Key Highlights

  • The PLATINUM-Truveta study included 2,873 adults with MASH who initiated semaglutide 2.4 mg.
  • At six months, semaglutide 2.4 mg was associated with a mean weight loss of 18.9 pounds, about 8%, compared with resmetirom.
  • At three months, AST declined 6.7 units with semaglutide, compared with 1.9 units with resmetirom.
  • Both studies were retrospective, and their results were presented at The Liver Meeting in Denver.

Novo Nordisk (NYSE:NVO) announced new real-world data on Wegovy 2.4 mg, a once-weekly semaglutide injection, in adults with metabolic dysfunction-associated steatohepatitis, known as MASH. The results come from two retrospective studies, PLATINUM-Truveta and RHODIUM-2, presented at the American Association for the Study of Liver Diseases' Liver Meeting 2026 in Denver. The company, headquartered in Plainsboro, New Jersey and Bagsvaerd, Denmark, said the findings help illustrate treatment outcomes in patients with the disease.

The PLATINUM-Truveta Study

PLATINUM-Truveta included 2,873 adults with MASH who started treatment with semaglutide 2.4 mg and 2,285 adults with MASH who started treatment with resmetirom. The adjusted outcomes were measured at three and six months. At three months, AST, a liver enzyme, fell by 6.7 units in the semaglutide group compared with 1.9 units in the resmetirom group, a difference with a p value below 0.001. ALT declined by 8.7 units compared with 4.8 units, although that difference did not reach statistical significance, with a p value of 0.077.

Body weight changes were larger in the semaglutide group, falling 10.5 pounds at three months compared with 1.5 pounds for resmetirom. HbA1c, a measure of blood sugar, decreased 0.29 percentage points with semaglutide, while it rose slightly with resmetirom. At six months, the company reported a mean weight loss from baseline of 18.9 pounds, or about 8%, for semaglutide relative to resmetirom, which it described as statistically significant.

The RHODIUM-2 Analysis

A separate analysis, RHODIUM-2, examined people who began semaglutide 2.4 mg compared with those who did not start the treatment. The company reported that patients who started semaglutide had greater one-year reductions in liver enzymes and body weight, along with a larger decrease in HbA1c, than patients who did not start it. The study design differs from a randomized trial, and the comparison groups reflect treatment decisions made in routine care.

Both analyses are retrospective. That design allows researchers to review existing patient records, but it cannot control for every Factor that influences treatment choices or outcomes, which limits how the results can be compared with controlled clinical trials.

Context Around the MASH Treatment Landscape

The company said the disease may progress without clear symptoms, which makes it important for clinicians and patients to understand how a treatment may affect the condition over time. Novo Nordisk's vice president of medical affairs said the findings offer insights into real-world results and are intended to inform providers.

Resmetirom is the comparator used in PLATINUM-Truveta, and the study was designed to set semaglutide against an established alternative treatment for the same condition. The company presented the results as real-world data intended to help inform providers, and it did not present them as a replacement for controlled trial findings.

MASH, or metabolic dysfunction-associated steatohepatitis, is a form of liver disease linked to metabolic conditions such as obesity and type 2 diabetes. Liver enzymes such as AST and ALT are commonly tracked in patients with the condition, and changes in these markers are one of several measures used in clinical and real-world research. The company's studies also measured weight and HbA1c, which matter for patients who have overlapping metabolic conditions.

Real-world studies use data from routine clinical care rather than from controlled trials with assigned treatments. They can show how a treatment performs across a broader set of patients, but they also carry limitations, including differences in who receives each treatment. The company presented PLATINUM-Truveta and RHODIUM-2 as real-world analyses, which places them in a different category from pivotal trial results.

Final Word

Novo Nordisk's real-world data on Wegovy 2.4 mg add to the body of observational evidence on liver enzymes, weight and blood sugar in adults with MASH. The PLATINUM-Truveta comparison shows changes in several measures over three and six months, while RHODIUM-2 compares patients who started treatment with those who did not. Because both studies are retrospective, the findings will be read alongside controlled trial results as clinicians and researchers review the evidence.