Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06919328

Absorption and Tolerability of Injectable Administration of Niagen®+, as Compared to NAD+

Absorption and Tolerability of Injectable Administration of Niagen®+, Nicotinamide Riboside Chloride, a Specialized Form of Vitamin B3, as Compared to NAD+: a Double Blinded, Randomized, Controlled Clinical Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Nutraceuticals Research Institute · Academic / Other
Sex
All
Age
40 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study evaluates the subjective effects of injection administration of NR on healthy adult populations.

Detailed description

The purpose of this work is to explore the tolerability of Niagen®, nicotinamide riboside chloride, a specialized form of vitamin B3, via intramuscular (IM), subcutaneous (SQ), and intravenous-push (IVP) administration, in comparison to NAD+, an active comparator, administered through the same routes.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTNiagen®nicotinamide riboside
OTHERNAD+Nicotinamide adenine dinucleotide
OTHERPlacebobacteriostatic water

Timeline

Start date
2024-10-31
Primary completion
2025-04-30
Completion
2025-06-30
First posted
2025-04-09
Last updated
2025-04-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06919328. Inclusion in this directory is not an endorsement.