Clinical Trials Directory

Trials / Completed

CompletedNCT05517122

Effect of Oral NAD+ Precursors Administration on Blood NAD+ Concentration in Healthy Adults

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
68 (actual)
Sponsor
Société des Produits Nestlé (SPN) · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Nicotinamide adenine dinucleotide (NAD) is a coenzyme playing a central role in human metabolic pathways. A recognized approach to increase NAD level is through oral supplementation of its precursors promoting NAD synthesis in vivo. NAD precursors exist in multiple forms. However, it is unclear how the various precursors compare in their ability to increase NAD levels in human blood. The purpose of this study is to compare the effect of 3 NAD precursors on whole blood NAD metabolome.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTNicotinamide (NAM)500 mg a day
DIETARY_SUPPLEMENTNicotinamide Riboside (NR)1000 mg a day
DIETARY_SUPPLEMENTNicotinamide Mono Nucleotide (NMN)1000 mg a day
DIETARY_SUPPLEMENTMicrocrystalline cellulose500 mg a day

Timeline

Start date
2022-07-12
Primary completion
2022-11-24
Completion
2022-11-24
First posted
2022-08-26
Last updated
2025-04-24

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT05517122. Inclusion in this directory is not an endorsement.