Assessing the Safety of an IGY Supplement on the Gut Microbiome

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorNimble Science Ltd.

About this trial

This study is to evaluate whether Muno-IgY is effective in enhancing immune health among adults over a six week period.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 18-65 years old at the inclusion of the study, both female and male subjects.

Signed Informed Consent; willing and able to comply with study procedures.

Willing to maintain their diet and physical activity levels during the study.

Able to swallow a 25mm x 9mm sized capsule

Disqualifiers

Use of regular prescription medications, including antihypertensives, anti-inflammatory drugs, corticosteroids, immunosuppressants, antidepressants, antipsychotics, anti-diabetic medications, and anti-arrhythmic agents, which in the opinion of the investigator, would adversely affect study safety or outcome.

Prior gastrointestinal disease, surgery, or radiation treatment which, in the Investigator's opinion, would lead to intestinal structuring or obstruction with a risk of capsule non-excretion, including, e.g., achalasia, eosinophilic esophagitis, cancer diagnosis or previous esophageal, gastric, small intestinal, or colonic surgery. Appendectomy or cholecystectomy more than 3 months before the screening visit is acceptable.

History of known structural gastrointestinal abnormalities such as structures or fistulas which may lead to mechanical obstruction.

Use of any medications in the week prior to the SIMBA or LIMBA capsule ingestions, unless part of regular treatment, that could substantially alter gastrointestinal motor function (e.g., opioids, anticholinergics, GLP-1 analogues); laxative and prokinetic use is allowed if it is kept unchanged in the week prior to the SIMBA and LIMBA capsule ingestions. Proton pump inhibitors (PPIs) are allowed provided a wash-out period of 48 hours is respected before swallowing the capsules and PPI treatment is resumed only 4 hours thereafter.

Trial design

Design model

Single group

Treatments tested in this trial

  • IgY supplement

    Dietary supplement

    Ingesting the immune supplement over the experimental period

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: IgY SupplementExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Primary Outcome

To assess the safety of Muno-IgY™ in the small intestine. By monitoring the number of participants with treatment-related adverse events as assessed by CTCAE v4.0

Time frame
Through study completion (Baseline to the end of the interventional period), an average of 6 weeks

Secondary outcomes

1

Secondary 1

Investigate the association or determine if changes in the small and large intestine occur and fecal microbiomes through metagenomic analysis

Time frame
Through study completion (Baseline to the end of the interventional period), an average of 6 weeks
2

Secondary 2

To assess the bioavailability of the Muno-IgY, using the SIMBA capsule as a tool for sample collection

Time frame
Through study completion (Baseline to the end of the interventional period), an average of 6 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nimble Science Ltd.

Lead sponsor

IGY Immune Technologies & Life Sciences Inc.

Collaborator

This trial is not recruiting at the moment. You can still explore other options: