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Dietary Supplement

Nicotinamide mononucleotide (NMN-C) for Healthy Subjects

N/A
Waitlist Available
Research Sponsored by Seneque SA
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Females of childbearing potential should be either sexually inactive (abstinent) for 60 days prior to the first dose of the study, throughout the study and for 30 days after completion of the study, or be using an acceptable methods of birth control.
BMI between 18.5 and 29.9 kg/m2; with a stable weight over the last 3 months (±2 kg).
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-dose and at 0.25, 0.5, 1, 2, 4, 8, 12 hour post-dose on day 29
Awards & highlights

Study Summary

This trial is investigating the safety and effects of a 30-day course of nicotinamide mononucleotide (NMN-C) in healthy adults.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-dose and at 0.25, 0.5, 1, 2, 4, 8, 12 hour post-dose on day 29
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-dose and at 0.25, 0.5, 1, 2, 4, 8, 12 hour post-dose on day 29 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Safety as measured by subject incident of treatment-emergent adverse events
Safety as measured by subject incident of treatment-emergent clinically significant changes in clinical laboratory safety tests.
Safety as measured by subject incident of treatment-emergent clinically significant changes in vital signs
Secondary outcome measures
Change from baseline in NAD+ and NMN concentrations in whole blood
Change from baseline in NAD+ metabolites concentrations in plasma
Change from baseline in NAD+ metabolites concentrations in urine
+8 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: NMN-CExperimental Treatment1 Intervention
Healthy individuals receiving NMN-C
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Nicotinamide mononucleotide (NMN-C)
2021
N/A
~50

Find a Location

Who is running the clinical trial?

Seneque SALead Sponsor
3 Previous Clinical Trials
237 Total Patients Enrolled
Dicentra Inc.Industry Sponsor
3 Previous Clinical Trials
260 Total Patients Enrolled
LGDIndustry Sponsor
6 Previous Clinical Trials
451 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Do my characteristics meet the criteria to join this medical experiment?

"This clinical trial seeks to recruit 24 participants with healthy BMI between 18.5 and 29.9 kg/m2 that have maintained their weight for the past 3 months (±2kg). Furthermore, post-menopausal women must present evidence of amenorrhea for a year before being eligible; whereas females capable of bearing children are expected to abstain from sexual activity or use effective birth control methods in order to be included in the study. Additionally, all patients will need to adhere to dietary guidelines issued by an assigned nutritionist both during and after completion of the experiment as well as consuming pre-established meals prior specified visits."

Answered by AI

Is eligibility limited to those under the age of 25 for this experiment?

"This clinical investigation is open to individuals aged 18 and above, up to the age of 65."

Answered by AI

Are there still vacancies in this research program?

"According to clinicaltrials.gov, this research endeavour is not presently enrolling patients; the trial was advertised on August 5th 2021 and its information was last updated on May 31st 2022. Despite that fact, there are currently 839 other studies actively seeking participants."

Answered by AI
~7 spots leftby Apr 2025