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Beta Glucan 500 and Biological Age and Immune Age

O

OvationLab

Status and phase

Not yet enrolling
Phase 2

Conditions

Aging

Treatments

Dietary Supplement: Beta Glucan

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT07104929
BWH-002

Details and patient eligibility

About

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).

Enrollment

60 estimated patients

Sex

All

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Beta Glucan
Experimental group
Treatment:
Dietary Supplement: Beta Glucan

Trial contacts and locations

1

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Central trial contact

Chris D'Adamo Principal Investigator, PhD

Data sourced from clinicaltrials.gov

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