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Beta Glucan 500 and Biological Age and Immune Age

Prospective Human Study Evaluating the Effects of Beta Glucan 500 on Markers of Biological Age and Immune Age: An Open-label Pilot Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07104929
Enrollment
60
Registered
2025-08-05
Start date
2025-05-14
Completion date
2025-10-09
Last updated
2026-02-19

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

Conditions

Aging

Keywords

aging, biological age, immunosenescence, beta glucan

Brief summary

The primary purpose of this study is to evaluate the effects of BWH Labs - Beta Glucan 500 on biomarkers of biological and immune age among healthy adults. A single-arm, open-label prospective study will be conducted evaluating the impact of 12 weeks of supplementation with two capsules daily of Beta Glucan 500 on a variety of validated markers of biological and immune age on the comprehensive TruAge panel (TruDiagnostics, Lexington, KY).

Interventions

DIETARY_SUPPLEMENTBeta Glucan

12 weeks of supplementation with two capsules daily of BWH Labs Beta Glucan 500

Sponsors

OvationLab
Lead SponsorNETWORK

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Adult females or males age ≥ 40 years 2. Ability to read and speak English 3. Previous completion of a TruDiagnostic TruAge test within the past three months to enable comparison of previous biomarkers to the same biomarkers after intervention 4. DunedinPACE estimate of aging \>0.9

Exclusion criteria

1. Current diagnosis and treatment for an autoimmune condition 2. Current use of beta-glucan or mushroom dietary supplement 3. Known allergies to beta glucan, yeast, or mushrooms 4. Currently pregnant or lactating women or women planning to become pregnant in the next 12 weeks 5. Current diagnosis of a chronic health condition (e.g., cancer, heart failure, history of pancreatitis, type I or II diabetics on insulin) deemed clinically contraindicated for the study protocol 6. Participants unable to provide consent

Design outcomes

Primary

MeasureTime frame
Epigenetic TestingChange from baseline to 12 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026