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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Niagen® | nicotinamide riboside |
| OTHER | NAD+ | Nicotinamide adenine dinucleotide |
| OTHER | Placebo | bacteriostatic 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.