Effects of TOTUM-448 on Liver Fat Content, Cardiometabolic Risk Factors and Gut Microbiota Among Participants with MASLD
Recruiting now NCT06704321
Run by Valbiotis · for 18 to 75 · All sexes · accepts healthy volunteers
What this study is about
This clinical trial aims to investigate the effects of TOTUM-448, a mix of 5 plant extracts and choline, consumed at the daily regimen of two times per day, on liver fat content, cardiometabolic risk factors and gut microbiota among both men and women with MASLD.
Who can join (things the study team will check)
✅ You may be able to join if…
- Men and women aged between 18 and 75 years (including ranges);
- CAP Score ≥288dB/m with liver stiffness results <8kPa (corresponding to F0 to F1 fibrosis score) assessed by Fibroscan®;
- BMI ≥25 and <40 kg/m2 and WC thresholds according to the NAFLD Nomenclature consensus group (Rinella. 2023. Hepatology);
- Weight stable within ± 5% in the last three months.
🚫 You may not be able to join if…
- Contraindications to MRI, Fibroscan® and DEXA;
- Suffering from a metabolic disorder susceptible to significantly affect glucose metabolism or plasma lipid levels or that might affect the study outcomes according to the investigator;
- Suffering from an uncontrolled arterial hypertension (systolic blood pressure ≥ 160 mmHg and/or diastolic blood pressure ≥ 100 mmHg);
- With a history of atherosclerotic cardiovascular disease (ASCVD);
- Taking medication which may affect the study outcomes;
- Alcohol consumption over ≥10 drinks/week for women and ≥15 drinks/week for men (women consuming more than 3 drinks/day and men consuming more than 4 drinks/day will also be excluded) or not agreeing to keep their alcohol consumption habits unchanged throughout the study.
Where this trial is running
- Institut sur la nutrition et les aliments fonctionnels (INAF), Québec, Quebec, Canada
Who to contact
Véronique Sapone, MSc · +33 (0)6 75 32 66 59 · veronique.sapone@valbiotis.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06704321.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
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