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A Study to Evaluate Vitamin B3 Derivative to Treat Mitochondrial Myopathy

Randomized, Double-blinded, Placebo-controlled Study Evaluating the Efficacy of Nicotinamide Riboside (NR) - a Vitamin B3 Derivative - for Treatment of Mitochondrial Myopathy Disorder

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05590468
Enrollment
34
Registered
2022-10-21
Start date
2023-05-26
Completion date
2026-11-01
Last updated
2026-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mitochondrial Myopathy

Brief summary

The purpose of this study is to determine the effects of Nicotinamide Riboside (NR) supplement in adult-onset symptoms of mitochondrial myopathy.

Interventions

DIETARY_SUPPLEMENTNicotinamide Riboside

Vitamin B3 derivative; a total of 1000 mg/day in a regimen of 500mg every 12 hours by mouth (either fasting or fed)

DRUGPlacebo

Looks exactly like the study drug, but it contains no active ingredient

Sponsors

Ralitza Gavrilova
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Biochemically and/or genetically confirmed or confirmed primary mitochondrial myopathy based on published diagnostic criteria. * Biochemically confirmed mitochondrial disorder would mean that the patient meets clinical criteria and has either biopsy or biochemical testing that supports the diagnosis. * Confirmed mitochondrial disorder means that the patient meets published clinical criteria for the diagnosis and has also had confirmatory genetic testing for the disorder type. * Agreed to avoid vitamin supplementation or nutritional products with vitamin B3 forms 14 days prior to the enrollment and during the study in order to not exceed 200 mg/day of vitamin B3 derivatives intake. * Female of childbearing potential agreed to use effective contraception throughout the study. * Written, informed consent to participate in the study.

Exclusion criteria

* Unwilling to comply with the follow-up schedule. * Inability or refusal to give informed consent by the patient or a legally authorized representative. * Known pregnancy or breastfeeding. * Concurrent participation in another investigational drug study or within washout period of treatment. * Presence of other medical symptoms or condition, which may interfere with interpretation of outcome measures as determined by the study PI. Clinical / Laboratory

Design outcomes

Primary

MeasureTime frameDescription
Changes in 6-Minute Walk Test PerformanceBaseline, 6 months, 12 monthsThe 6-minute walk test (6MWT) quantifies the distance a person can walk in six minutes. Measured in meters.

Secondary

MeasureTime frameDescription
Change in skeletal muscle functionBaseline, 6 months, 12 monthsMeasured using the Short Physical Performance Battery (SPPB) score based on timed measures of standing balance, walking speed and ability to rise from a chair. Each of the 3 performance measures will be assigned a score ranging from 0 to 4, with 4 indicating the highest level of performance and 0 the inability to complete the test. A summary score (range 0-12) will be subsequently calculated by adding the 3 scores.
Change in skeletal muscle strengthBaseline, 6 months, 12 monthsMeasured using the strength one repetition maximum (1RM leg press) defined as the maximal weight an individual can lift for only one repetition with correct technique.
Change in isometric strength of trunk flexorsBaseline, 6 months, 12 monthsAssessed by generated maximum force against a stationary dynamometer reported in kilograms of force. Trunk flexion strength tested in the supine position with knees slightly bent, arms at side and head in midline. The base of the dynamometer will be placed on the middle of the sternum and the patient will be instructed to exert isometric force by lifting both scapula off the plinth.
Change in isometric strength of trunk extensor muscleBaseline, 6 months, 12 monthsAssessed by generated maximum force against a stationary dynamometer reported in kilograms of force. Trunk extensor muscle strength tested in prone position. The base of the dynamometer will be placed at the level of the T4 spine and the patient instructed to generate an isometric force by lifting the chest off the plinth. After sufficient practice in the standardized positions, 5 trials will be recorded in each position.
Change in maximal oxygen uptake (VO2 max)Baseline, 6 months, 12 monthsMaximal oxygen uptake (VO2 max) test measures the maximum rate of oxygen consumption during incremental exercise (exercise of increasing intensity) and reflects the cardiorespiratory fitness of an individual. Reported in ml/kg/min.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRalitza H. Gavrilova, MD

Mayo Clinic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026