Vitamin B3 supplement put to the test against psoriasis inflammation
NCT ID NCT04271735
First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time
Summary
Researchers are testing whether nicotinamide riboside, a form of vitamin B3 sold as a supplement, can reduce immune system activation in people with mild to moderate psoriasis. The trial enrolls adults aged 18 to 80 who are not on biologic therapy. Participants take either the supplement or a placebo twice daily for four weeks, and researchers measure changes in specific immune cells and skin inflammation.
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 taken as a dietary supplement
- What this could lead to
- If it works, nicotinamide riboside could offer a low-cost supplement option for calming the immune activation that drives psoriasis and related heart risks.
- What could go wrong
- This is a small pilot study of 29 people taking the supplement for only four weeks. The results may not hold up in larger trials, and the supplement may not change immune activity enough to matter.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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29 people
The number who actually took part.
- Started
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Aug 2020
- Finished
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Dec 2022
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
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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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
-
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: Individuals must meet all inclusion criteria listed below in order to be eligible to participate in the study. * Males and females between the ages of 18 and 80 with mild to moderate active psoriasis. * Female subjects of child-bearing ability willing to commit to reliable contraception while participating in the study. * Ability to provide informed consent * Willingness and ability to participate in required study procedures EXCLUSION CRITERIA: * Severe psoriasis by PASI (Psoriasis Area and Severity Index) score \> 12 * Currently being treated with biologic immune modifying agents. * Currently on treatment for allergies or other inflammatory diseases. * Currently taking a multivitamin, Vitamin B or tryptophan supplementation and unwilling to stop within 2 weeks of baseline visit. * Unwillingness/inability to provide informed consent * ALT \> x3 upper limit of normal, hepatic insufficiency or active liver disease * Recent history of acute gout * Chronic renal insufficiency with creatinine \> 2.5mg/dl * Pregnant (or attempting to become pregnant) women * Current participation in another drug study * History of intolerance to NR precursor compounds, including niacin or nicotinamide * Study adherence concerns * Individuals with diabetes type 1 and 2 who use insulin * Women of child-bearing potential unwilling to use contraception or unwilling to practice abstinence * Breastfeeding women unwilling to stop breastfeeding * Immunization administered within 30 days of participation and no plans for immunization while participating in the study
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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
-
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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