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NCT06889740

Evaluate the Safety, Tolerability, and Efficacy of UthPeak NMNH (Reduced Nicotinamide Mononucleotide) in Healthy Adult Participants

Completed NA Last updated 4 July 2025
What this trial tests

NA trial testing NMNH in Healthy Aging in 80 participants. Completed in 25 January 2025.

Timeline
8 July 2024
Primary endpoint
8 December 2024
25 January 2025

Quick facts

Lead sponsorEffePharm LTD
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeother
Enrollment80
Start date8 July 2024
Primary completion8 December 2024
Estimated completion25 January 2025
Sites2 locations across India

Drugs / interventions tested

Conditions studied

Sponsor

EffePharm LTD

Who can join

Adults 40 to 65, any sex, with Healthy Aging. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is to assess the safety and tolerability of NMNH as a dietary supplement for human consumption. The current study aims to comprehensively evaluate its potential effects on pharmacokinetics, physical performance, biological age and overall quality of life. These findings will expand our understanding of NMNH therapeutic potential and guide its future clinical applications in anti-aging interventions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Healthy Aging

Currently open trials in the same condition.

Other EffePharm LTD trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06889740.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing