Phase 2Completed

NAD+ Precursor Supplementation in Friedreich's Ataxia

A Phase 2a Study of NAD+ Precursor Supplementation in Friedreich's Ataxia

Sponsor
Metro International Biotech, LLC (Industry)
Enrolment
7 enrolled
Conditions
Friedreich Ataxia
Interventions
MIB-626
Ages
adults
Registry
NCT04817111

From the registry

The primary objective is to test the safety and tolerability of short-term therapy with a nicotinamide adenine dinucleotide (NAD+) precursor (MIB-626) in adults with Friedreich's Ataxia (FA) without overt heart failure and with a left ventricular ejection fraction ≥ 40%. A key secondary objective is to test the effects of MIB-626 on cardiac and skeletal muscle bioenergetics.

Primary outcomes

  • Percentage of Individuals With Treatment-emergent Adverse Events as Assessed by Common Terminology Criteria for Adverse Events Version 5.0.
Full record on ClinicalTrials.gov