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Clinical Trial Summary

The purpose of this study is to assess an effective single oral supplement or combination of oral supplements for increasing whole blood NAD+ levels.


Clinical Trial Description

This is a open-label dose finding study to detect an effective single oral supplement or combination of oral supplements for enhancing whole blood levels of NAD+. Each subject will receive a specific dose of the formulation once daily for 3 days followed by a washout period. Upon completion of the treatment phase, there is a post-treatment period of assessments.

Participants receive assessments of blood tests, vital signs, body weight with completion of questionnaires.

The primary objective of the study is to identify the ideal dosage of an oral supplement to increase whole blood NAD+ levels in adults.

The secondary objective of the study is to monitor for safety from a change in fasting blood chemistry panel parameters after three day's dosing compared to cycle baseline. ;


Study Design


Related Conditions & MeSH terms

  • Increase in Blood Levels of Nicotinamide Adenine Dinucleotide (NAD+)

NCT number NCT03707652
Study type Interventional
Source Supplement Formulators, Inc.
Contact
Status Completed
Phase N/A
Start date March 12, 2018
Completion date May 24, 2018