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Stimulating Adipose Tissue Fatty Acid Disposal With Low-dose, Postprandial, Intermittent Niacin for the Treatment of Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD).

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Metabolic dysfunction-associated steatotic liver disease (MASLD) (aka non-alcoholic fatty liver disease), commonly occurring in individuals with obesity and type 2 diabetes can lead to liver inflammation/ fibrosis. MASLD results from fat being disproportionately deposited in the liver. The goal of this mechanistic study is to investigate metabolic response in patients aged 50 to 80 years with non-alcoholic fatty liver disease, after niacin (vitamin B3) treatment. The main questions it aims to answer are: * Does Niacin lower the fat deposition in the liver? * Does Niacin raise White Adipose Tissue storage of dietary fatty acids? Researchers will compare Niacin to a placebo (a look-alike substance that contains no drug) to compare the metabolic response. Duration of study per participant: Up to 28 weeks

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 80
Healthy Volunteers: f
View:

• aged 50 to 80 years;

• diagnosed with MASLD, defined as the presence of liver steatosis + abdominal obesity (as defined by the International Diabetes Federation country/ethnic group-specific criteria;

• all women will be post-menopausal.

Locations
Other Locations
Canada
Centre de recherche du CHUS
RECRUITING
Sherbrooke
Contact Information
Primary
Frédérique Frisch
frederique.frisch@usherbrooke.ca
1-819-346-1110
Time Frame
Start Date: 2026-04
Estimated Completion Date: 2030-07
Participants
Target number of participants: 36
Treatments
Placebo_comparator: Placebo group
It will be a 12-week treatment phase. The placebo treatment will be administered once daily, at the end of the largest meal.
Active_comparator: Niacin group
It will be a 12-week treatment phase. The treatment will be administered once daily, at the end of the largest meal.
Sponsors
Leads: Université de Sherbrooke
Collaborators: Centre hospitalier universitaire de Québec- Université Laval, Centre de recherche du Centre hospitalier universitaire de Sherbrooke

This content was sourced from clinicaltrials.gov