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A planned trial of trigonelline supplements in healthy adults aged 40 to 70

Opening soon · PHASE 1 · dsm-firmenich Switzerland AG

What this means

This trial plans to test four doses of a supplement against a placebo and a similar supplement, NMN. It has not started yet and has no results, so it cannot yet show whether the supplement works.

Plain-English summary written by an AI model from the registry listing.

Status
Opening soon
Who can join
Ages 40–70 · 60 healthy adults aged 40 to 70
Where
1 site

Contacts and how to join ↗

The science

Registered title
Effects of Trigonelline Monohydrate on NAD+ Metabolism, Pharmacokinetics, Safety, and Tolerability in Healthy Adults
Phase
PHASE 1
Study type
interventional
Conditions
NAD+ Metabolism, Pharmacokinetics, Bioavailability, Healthy Adults
What is tested
Nicotinamide Mononucleotide (NMN), Placebo, Trigonelline Monohydrate
Sponsor
dsm-firmenich Switzerland AG
Ages
40 Years to 70 Years
Dates
First posted Oct 19, 2026 · updated Oct 19, 2026

Registry summary

This Phase 1 study is designed to evaluate the pharmacokinetic, pharmacodynamic, bioavailability, safety, and tolerability effects of trigonelline monohydrate in generally healthy adults aged 40 to 70 years. Sixty participants will be randomized in a double-blind, parallel-arm study to receive one of four doses of trigonelline monohydrate (equivalent to 150 mg, 300 mg, 450 mg, or 600 mg of trigonelline daily), an active comparator (600 mg nicotinamide mononucleotide [NMN]), or placebo for 4 weeks.

The primary objective is to assess the effect of trigonelline monohydrate supplementation on NAD+ metabolism by measuring the change from baseline in whole blood NAD+ concentrations after 4 weeks of supplementation. Secondary objectives include evaluation of trigonelline pharmacokinetics, bioavailability, plasma accumulation following repeated dosing, effects on NAD-related metabolites, and urinary excretion of trigonelline and NAD-related metabolites. Safety and tolerability will be assessed through adverse events, vital signs, anthropometric measurements, and clinical laboratory assessments. Exploratory analyses will examine inflammatory biomarkers and additional NAD-related metabolic outcomes.

Sites (1)

  • Apex Trials, Guelph, Ontario - on, Canada

Related treatments

NAD+ boosters · NMN (nicotinamide mononucleotide)

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