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Clinical Trial Summary

A single-center, randomized, placebo-controlled study in community dwelling, healthy, regularly exercising, highly physically fit men and women, 19 to 40 years. Eligible participants will be randomized to receive either 1000 mg NMN or placebo twice daily for 10 weeks.


Clinical Trial Description

The study participants will be screened for potential participation and those meeting eligibility criteria on screening will be offered participation in the study. 120 subjects will be block randomized in a 1:1:1:1 ratio, stratified by sex (male, female) and baseline VO2 max. Participants will be randomly assigned to one of four groups using a 2 by 2 factorial design: Group 1 - MIB-626 (MIB-626 - UPA) plus usual physical activity; Group 2 - standardized, progressive, high intensity, multidimensional exercise plus placebo (PL-Ex); Group 3 - MIB-626 plus standardized, progressive, high intensity, multidimensional exercise (MIB-626-Ex); Group 4 - placebo plus usual physical activity (PL-UPA). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05878119
Study type Interventional
Source Metro International Biotech, LLC
Contact John Gauthier
Phone 617-525-9136
Email jgauthier5@bwh.harvard.edu
Status Recruiting
Phase Phase 2
Start date October 25, 2023
Completion date June 2025

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