Could a vitamin pill slow Parkinson's? major trial tests nicotinamide riboside
NCT ID NCT03568968
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed Phase 3 trial tested whether a daily supplement called nicotinamide riboside (a form of vitamin B3) can slow the progression of early Parkinson's disease. 410 people with early-stage Parkinson's took either the supplement or a placebo for 52 weeks. Researchers measured changes in motor and non-motor symptoms using a standard rating scale. The goal was to see if replenishing a key cellular energy molecule (NAD) could help protect brain cells.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nicotinamide riboside (a form of vitamin B3)
- What this could lead to
- If it works, this could point toward a way to slow the progression of early Parkinson's disease using a simple dietary supplement.
- What could go wrong
- This is a completed Phase 3 trial, but results are not yet published. The supplement may not slow the disease, and benefits may be small or not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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410 people
The number who actually took part.
- Started
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May 2020
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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35 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Have a clinical diagnosis of idiopathic PD according to the MDS clinical diagnostic criteria for Parkinson's disease * \[¹²³I\]FP-CIT single photon emission CT (DaTscan) confirming nigrostriatal degeneration * Diagnosed with PD within 2 years from enrolment * Hoehn and Yahr score \< 3 at enrolment * Optimal symptomatic therapy, not requiring adjustments, for at least 1 month. * Age equal to or greater than 35 years at time of enrolment. Exclusion Criteria: * Dementia or other neurodegenerative disorder at baseline visit * Diagnosed with atypical parkinsonism or vascular parkinsonism * Any psychiatric disorder that would interfere with compliance in the study. * Any severe somatic illness that would make the individual unable to comply and participate in the study. * Use of high dose vitamin B3 supplementation within 30 days of enrolment * Metabolic, neoplastic, or other physically or mentally debilitating disorder at baseline visit. * Genetically confirmed mitochondrial disease
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Akershus university hospital
Oslo, Norway
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Arendal Hospital
Arendal, Norway
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Bodø Hospital
Bodø, Nordland, Norway
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Førde sykehus
Førde, Norway
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Haugesund Hospital
Haugesund, Norway
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Haukeland University Hospital
Bergen, Norway
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Molde sjukehus
Molde, Norway
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Oslo University Hospital
Oslo, Norway
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University Hospital of North Norway
Tromsø, Norway
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Vestre Viken Hospital
Drammen, Norway
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Østfold Hospital
Fredrikstad, Østland, Norway
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