Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07471048

A Study to Evaluate the Impact of a Magnolia Officinalis Dietary Supplement on Immune Biomarkers in Subjects With Psoriasis

A Decentralized, Randomized Interventional Study to Evaluate the Impact of an Over-the-Counter Magnolia Officinalis Oral Supplement on Blood Biomarkers of Immune Activation in Subjects With Psoriasis

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Sirt3 LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to evaluate whether Viv, a consumer-grade dietary supplement derived from the Magnolia officinalis plant, has an effect on biomarkers of immune activity in adults with psoriasis. To address this question, this trial will compare Viv to a placebo (a look-alike substance that contains no drug). Participants will: * Take Viv or a placebo every day for 3 months. * Complete electronic questionnaires about their quality of life and psoriasis symptoms at the beginning of the study and again at 1 months and 3 months. * Be provided with at home blood collection kits, which they will use to collect blood at the beginning of the study and again at 1 months and 3 months. Researchers will analyze these blood samples to measure the levels of specific inflammatory proteins and evaluate how they change over the course of the study in the participants taking Viv compared to those taking placebo.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOral supplement containing 200mg Magnolia officinalis bark extractViv is a consumer grade oral supplement containing 200mg Magnolia officinalis bark extract encapsulated in a hypromellose capsule.
DIETARY_SUPPLEMENTPlaceboOral hypromellose capsule with all inactive ingredients but lacking the Magnolia officinalis bark extract

Timeline

Start date
2026-03-01
Primary completion
2028-09-01
Completion
2029-09-01
First posted
2026-03-13
Last updated
2026-03-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07471048. Inclusion in this directory is not an endorsement.