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Study identifier: NCT07144527 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Nicotinamide Mononucleotide Supplementation for Exercise Tolerance Improvement in Healthy Older Adults

Condition: Aging · Frailty · Exercise Tolerance  ·  Sponsor: Scott Silveira

PhaseNA
Planned participants40
Who can joinAll sexes, 60 Years to 80 Years
Healthy volunteersYes

About this study

This is a randomized, double-blind, placebo-controlled, two-arm crossover clinical trial evaluating the effects of a patented age-reversal therapy, EGA®, compared to conventional nicotinamide mononucleotide (NMN) supplementation. The study will assess safety and efficacy in improving exercise tolerance and modulating biomarkers of aging in healthy older adults. The primary outcome is cycle ergometry constant work rate (CWR) exercise tolerance, measured as time to fatigue. Secondary outcomes include changes in peak oxygen consumption (VO₂peak), critical power, anaerobic work capacity, lactate threshold, and NAD⁺ metabolite levels. EGA® is composed of three metabolomic compounds that are endogenous to humans. The formulation has been used in prior exploratory studies and real-world applications, which have helped inform the design of this current trial.

This description comes directly from the study's public registry record.

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Locations (1)

Medical Office of Dr. Robert Huizenga MDBeverly Hills, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07144527