Recruiting

Viv

Sponsor:

Sirt3 LLC

Code:

NCT07471048

Conditions

Psoriasis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Oral supplement containing 200mg Magnolia officinalis bark extract

Placebo

Study Details

Brief 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

Psoriasis

Study ID

NCT07471048

Start date

Mar 1, 2026

Status verified date

Mar, 2026

Completion date

Sep 1, 2029

Anticipated

Primary completion date

Sep 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Male of female, aged 18 years or older at time of consent.
  • Diagnosis of stable psoriasis affecting for at least 6 months confirmed by a dermatologist.
  • Patients with psoriasis-associated comorbidities including psoriatic arthritis are permitted, as long as those comorbidities are not severe enough to require treatment with systemic therapies as defined in the exclusion criteria.
  • Able to read and understand English.
  • Able to read, understand, and provide informed consent.
  • Able to use a personal smartphone device and download Chloe by People Science.
  • Able to receive shipment of the product at an address within the United States.
  • Able to adhere to study protocol (e.g., willing to collect and ship blood samples)

Exclusion Criteria:

Any potential participants who:

  • Do not have a personal smartphone, internet access, or unwilling to download Chloe.
  • Prior treatment with any systemic non-biologic immunosuppressive agents (e.g., methotrexate, cyclosporine, azathioprine) within 8 weeks prior to randomization.
  • Prior treatment with any systemic biologic therapies (e.g., guselkumab, risankizumab, ustekinumab, secukinumab, brodalumab, infliximab, adalimumab, golimumab, etanercept) within 6 months prior to randomization
  • Prior treatment with any other systemic investigational drugs within 6 months prior to randomization.
  • Other Illnesses or Conditions: Participants who have the following comorbidities or gastrointestinal illnesses are excluded:
  • Currently pregnant, planning to become pregnant in the next 3 months, or breastfeeding
  • Any underlying medical conditions or comorbidities that may confound the assessment of digestive symptoms or the evaluation of the study outcomes.
  • Have a significant illness, disease or condition which, in the opinion of the principal investigator, may impact their ability to participate in the study or impact the study outcomes.
  • Known hypersensitivity or previous allergic reaction to magnolia, rice or hypromellose.
  • Are unlikely for any reason to be able to comply with the trial or considered unsuited for participation in the study by the Principal Investigator.

Study Design

Enrollment

100 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: Viv

Magnolia officinalis study arm

placebo comparator: Placebo

Placebo control study arm

Interventions

Oral supplement containing 200mg Magnolia officinalis bark extract

Viv is a consumer grade oral supplement containing 200mg Magnolia officinalis bark extract encapsulated in a hypromellose capsule.

Placebo

Oral hypromellose capsule with all inactive ingredients but lacking the Magnolia officinalis bark extract

Primary outcome measure

  • Relative change in plasma Beta defensin 2 from baseline [ Time Frame: From baseline to the end of study product/placebo use at 12 weeks ]

Central Contacts and Locations

Central contacts

Adeeb Rahman, PhD

2013596845clinicaltrial@takeviv.com

Locations

Decentralized Study Coordinating Center

Recruiting

Englewood, New Jersey, United States, 07631

Contacts

Viv Clinical Trial Operations

clinicaltrial@takeviv.com

More Information

Sponsor

Sirt3 LLC

Last update posted

Mar 13, 2026

Last verified

Mar, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Sirt3 LLC on 2026-03-13.