A Study of the Pharmacokinetics of Three Dosages of Niagen in Healthy Subjects

NCT ID: NCT02191462

Last Updated: 2014-09-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-07-31
• Study Completion Date: 2014-08-31

Brief Summary

The purpose of this study in to analyse the way in which the body processes Niagen (nicotinamide riboside) in healthy people. Blood and urine samples from subjects who are given a dose of Niagen will be analyzed for metabolites over the 24 hours after taking the dose.

Conditions

Pharmacokinetics

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: TRIPLE

Study Groups

Niagen 100mg

1 Niagen capsule (1 x 100 mg capsule) and 9 Placebo capsules

Group Type: EXPERIMENTAL

Niagen 100mg

Intervention Type: DIETARY_SUPPLEMENT

Niagen 300mg

3 Niagen capsules (3 x 100mg capsule) and 7 Placebo capsules

Group Type: EXPERIMENTAL

Niagen 300mg

Intervention Type: DIETARY_SUPPLEMENT

1000mg Niagen

10 Niagen capsules (10 x 100mg capsule)

Group Type: EXPERIMENTAL

Niagen 1000mg

Intervention Type: DIETARY_SUPPLEMENT

Interventions

Niagen 100mg

Intervention Type: DIETARY_SUPPLEMENT

Niagen 300mg

Intervention Type: DIETARY_SUPPLEMENT

Niagen 1000mg

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Healthy Male or female age 30-55 years
• BMI 18.5-29.9 kg/m2
• If female, subject is not of child bearing potential, OR Females of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result.
• Healthy as determined by laboratory results and medical history
• Agrees to maintain current level of physical activity throughout the study
• Agrees to avoid vitamins and St. John's Wort for 30 days prior to enrollment and during the study
• Agrees to avoid nutritional yeast, whey proteins, energy drinks, dairy products, grapefruit and grapefruit juice and alcohol 7 days prior to enrollment and during study
• Has given voluntary, written, informed consent to participate in the study

Exclusion Criteria

• Women who are pregnant, breastfeeding, or planning to become pregnant during the course of the trial.
• Use of natural health products (NHPs)/dietary supplements within 7 days prior to randomization and during the course of the study.
• Use of vitamins or St. John's Wort in the last 30 days before the study enrollment,
• Use of natural health products containing Nicotinamide riboside within 7 days prior to randomization and during the course of the study
• Use of nutritional yeast, whey proteins, energy drinks, grapefruit and grapefruit juice, dairy products, alcohol for 7 days prior to the study
• Subjects who are smokers
• Subjects with blood pressure ≥140/90
• Use of blood pressure medications
• Use of cholesterol lowering medications
• Metabolic diseases or chronic diseases
• Use of acute over the counter medication within 72 hours of test product dosing
• Unstable medical conditions as determined by the Qualified Investigator
• Immunocompromised individuals such as subjects that have undergone organ transplantation or subjects diagnosed with human immunodeficiency virus (HIV)
• Clinically significant abnormal lab results at screening (e.g. AST and/or ALT > 2 x ULN, and/or bilirubin > 2 x ULN) will be assessed by the Medical Investigator
• Subjects who have planned surgery during the course of the trial
• History of or current diagnosis of any cancer (except for successfully treated basal cell carcinoma) diagnosed less than 5 years prior to screening. Subjects with cancer in full remission more than 5 years after diagnosis are acceptable
• History of blood/bleeding disorders
• Blood donation in the past 2 months
• Alcohol abuse (>2 standard alcoholic drinks per day) or drug abuse within the past 6 months
• Participation in a clinical research trial within 30 days prior to randomization
• Allergy or sensitivity to study supplement ingredients or to any food or beverage provided during the study
• Individuals who are cognitively impaired and/or who are unable to give informed consent.
• Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures or which may pose significant risk to the subject

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

ChromaDex, Inc.

INDUSTRY

Sponsor Role: collaborator

KGK Science Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dale Wilson, MD

Role: PRINCIPAL_INVESTIGATOR

KGK Science Inc.

Locations

KGK Synergize Inc.

London, Ontario, Canada

Countries

Canada

Other Identifiers

14NBHC

Identifier Type: -

Identifier Source: org_study_id