ClinConnect ClinConnect Logo
Search / Trial NCT05369585

Mode of Action (MoA) Study of TOTUM-63 in Individuals at Increased Cardio-metabolic Risk

Launched by VALBIOTIS · May 5, 2022

Trial Information

Current as of May 27, 2025

Completed

Keywords

Dysglycemia Prediabetes Diabetes Risk Cardio Metabolic Risk Diet Supplement Plant Extracts Polyphenols Microbiota Magnetic Resonance Imaging

ClinConnect Summary

In 2019, over 460 million adults had diabetes worldwide. Moreover, it was estimated by the International Diabetes Federation that about 700 million adults will have type 2 diabetes (T2D) by 2045. Valbiotis is a research \& development company dedicated to scientific innovation for preventing and reducing the risk of metabolic and cardiovascular disease (CVD) using specific combinations of plant-based molecules. Valbiotis developed a formula (TOTUM-63) which is composed by the association of five plant extracts.

Given the results obtained in pre-clinical studies, as well as the good toleran...

Gender

ALL

Eligibility criteria

  • Main Inclusion Criteria:
  • Body mass index (BMI) between ≥ 27 and \< 40 kg/m2 kg/m²;
  • Waist circumference \> 94 cm for men and \> 80 cm for women;
  • Weight stable within ± 5% in the last three months;
  • Fasting plasma TG ≥ 1.35 OR fasting glycemia ≥ 5.6 and ≤ 6.9 mmol/L OR HbA1c ≥ 5.6 and ≤ 6.4 %
  • Main Exclusion Criteria:
  • Any metabolic disorder requiring pharmacological treatment and susceptible to affect glucose metabolism or plasma lipid levels or that might affect the study outcomes according to the investigator;
  • Taking medication which may affect the study outcomes (or a medication modification less than 3 months prior to the study);
  • To have taken regularly natural health products or enriched foods susceptible to modify the parameters followed by the investigator within the 3 months prior to the study;
  • With a known or suspected food allergy, intolerance or hypersensitivity to any of the study products' ingredient as well as the non-medicinal ingredients of the product;
  • Consuming more than 4 drinks of alcohol per week;
  • Having a lifestyle deemed incompatible with the study according to the investigator including high level of physical activity (defined as more than 10 hours of intense physical activity a week, walking excluded);
  • Pregnant or lactating women or intending to become pregnant within the timeframe of the study;
  • Fasting blood triglycerides (TG) \> 2.5 mmol/L;
  • Fasting blood LDL-C \> 4.9mmol/L or non-HDL-C \> 5.7 mmol/L;
  • Blood AST ≥ 45 U/L for men; and blood AST ≥ 35 U/L for women;
  • Blood ALT ≥ 60 U/L for men; and blood ALT ≥ 50 U/L for women;
  • Blood GGT ≥ 75 U/L for men; and blood GGT ≥ 50 U/L for women;
  • Blood creatinine concentration \> 125 μmol/L AND Estimated Glomerular Filtration Rate (eGFR) (calculated by Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula) \< 60 mL/min/1.73m²;
  • Complete blood count (CBC) with hemoglobin \< 120 g/L or leucocytes \< 3000 /mm3 or leucocytes \> 16000 /mm3 or clinically significant abnormality according to the investigator.

About Valbiotis

Valbiotis is a pioneering biotechnology company focused on the development of innovative nutritional solutions aimed at preventing and managing metabolic disorders. With a strong emphasis on research and development, Valbiotis harnesses advanced scientific expertise to create products that address health challenges such as obesity, diabetes, and cardiovascular diseases. The company is committed to conducting rigorous clinical trials to validate the efficacy and safety of its formulations, positioning itself at the forefront of preventive health solutions and contributing to a healthier future through evidence-based interventions.

Locations

Quebec, , Canada

Patients applied

0 patients applied

Trial Officials

André Marette, PhD

Principal Investigator

Laval University

Patrick Couture, MD FRCP PhD

Principal Investigator

Laval University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials