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evaluate the safety and immunomodulatory efficacy of Byolic CC supplement

A Clinical trial to evaluate the safety and immunomodulatory efficacy of Byolic CC supplement compared to placebo in healthy adults

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240304061158N4
Enrollment
90
Registered
2024-08-22
Start date
2024-08-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Immunomodulatory effect on healthy volunteers.

Interventions

Intervention 1: Intervention group: healthy volunteers take Byolic CC capsules produced by Behpad Tab for 2 months, once a day, preferably with meals. Intervention 2: Control group: healthy volunteers

Sponsors

Behpad Teb Iranian
Lead Sponsor
Shahed university Immune Response Regulation Research Center
Collaborator

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Health of volunteers

Exclusion criteria

Exclusion criteria: usage of immunosuppressive drugs, including cytotoxic drugs and corticosteroids, or any other drug (within 4 weeks before the start of the study) that may interfere with the supplement used in this study (or other herbal products) drug and food allergies pregnancy and lactation cardiovascular, kidney, lung, liver, endocrine, hematological, neurological or psychiatric diseases, etc.)

Design outcomes

Primary

MeasureTime frame
Safety check variables:Physical examination, vital signs and laboratory measurements including blood biochemistry (BC) and complete blood count (CBC). Timepoint: Day 0,30,60. Method of measurement: Physical examination, Blood test.;Variables for investigating the immunomodulatory effect: Measuring the levels of cytokines TNF-a and IL-12 in serum samples by ELISA method, Measuring the level of cytokine IFN-? in the supernatant, Measuring the proliferation and activation of NK cells by flow cytometry using FITC-a-human CD56 and PE-a-human CD314 (NKG2D) antibodies. Timepoint: Day 0 and 60. Method of measurement: Serum sample analyze.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzade Rashidi

Immunoregulation Research Center

a.rashidi@shahed.ac.ir+98 21 6641 9712

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026