Biobran/MGN-3 Increases Innate Resistance and Reduces the Incidence of Influenza-like Illnesses
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT04646980 |
Recruitment Status :
Completed
First Posted : November 30, 2020
Last Update Posted : November 30, 2020
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Influenza-like Illness | Dietary Supplement: Biobran/MGN-3 Other: Placebo | Not Applicable |
The current study investigated the effect of oral supplementation with Biobran/MGN-3, 500 mg every day for 3 months, on several components of innate immune system and the incidence rate of influenza-like illnesses (ILI) in older adults population. The study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki and was approval by Institutional Review Board (IRB) at the Faculty of Medicine, Zagazig University, Egypt. Zagazig University Hospitals serves over 1 million residents in Zagazig district and neighboring towns.
The study spanned the time period from November 2018 till the end of February 2019, a period with known peak incidence of ILI attacks. Subjects of ≥ 56 years were recruited from the visitors of outpatient clinics at Zagazig University Hospitals. The age of ≥ 56 years was used by the WHO to define old age in African nations. In addition, this age is close to public service retirement in Egyptian society, which is associated with significant social, mental, and psychological stress and therefore could be associated with significant decline in NK cell activity. Only local residents of Zagazig district were recruited to the study so as to reduce the dropout rate.
Originally 90 subjects, both males and females, were approached but only 80 subjects, 40 males and 40 females, continued the study. Ten of the recruits refused to participate when they realized that the sachets were only labeled with the manufacture symbols without printed names, which was used to ensure double-blinding. Informed consents were obtained from all participants and their right to unconditionally withdraw from the study at any time were made clear to them.
Males and females were randomly assigned into two groups (n=40/group) that received either placebo or Biobran/MGN-3 (500 mg/day for 3 months). Both the health care giver and the participants were blinded to the ingested supplement. Participants' health was monitored via weekly home visits and they were instructed to report any complaints or side effects by phone to the health care giver.
Diagnosis of ILI was made by documenting the incidence of acute respiratory illness with a measured temperature of ≥ 38 °C with cough (3). After diagnosis, the subject was helped to follow the proper health management plan by the health care giver. During the study, all participants were required not to take any vitamins or medications during the study without consultation.
The effect of Biobran/MGN-3 on liver, kidney, and hematological parameters were monitored. Liver functions were monitored using alanine aminotransferase (ALT/SGPT) and aspartate aminotransferase (AST/SGOT), whereas kidney function was monitored using serum uric acid. The assessed hematological parameters included red blood cell count (RBC), hematocrit value (HCT), hemoglobin (Hb), mean corpuscular hemoglobin (MCH), mean corpuscular volume (MCV), and total and differential (WBC).
NKC activity was measured using the well documented degranulation assay. The viral nucleic acid receptors, RIG-1 and MDA5, and their downstream target, ISG15 and MX1, were assessed using flowcytometry in BEAS-2B cells.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 80 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | Randomized double-blind placebo-controlled |
Masking: | Double (Participant, Care Provider) |
Masking Description: | Double (Participant, Care Provider) |
Primary Purpose: | Prevention |
Official Title: | Dietary Supplementation With Biobran/MGN-3 Increases Innate Resistance Against Viral Infections That Cause Influenza-like Illnesses in Elderly Subjects: a Randomized, Double-blind, Placebo-controlled Clinical Trial |
Actual Study Start Date : | November 28, 2018 |
Actual Primary Completion Date : | February 28, 2019 |
Actual Study Completion Date : | February 28, 2019 |

Arm | Intervention/treatment |
---|---|
Experimental: Biobran/MGN-3
This arm consisted from 20 males and 20 females. Biobran/MGN-3 was orally supplemented at dose of 500 mg per day for 3 months (end of November 2018- end of February 2019).
|
Dietary Supplement: Biobran/MGN-3
Biobran/MGN3 is defined by the Medicines and Healthcare products Regulatory Agency (MHRA) as a food supplement. Biobran/MGN3 is manufactured by hydrolyzing rice bran with the enzymatic extract of medicinal Shiitake mushrooms. Enzyme hydrolysis of rice bran produces arabinoxylane, a hemi-cellulose compound, which constitutes the active ingredient of biobran/MGN3. |
Placebo Comparator: Placebo
This arm consisted from 20 males and 20 females. Placebo, with the same appearance and taste, was orally supplemented at dose of 500 mg per day for 3 months (end of November 2018- end of February 2019).
|
Other: Placebo
Placebo, with same appearance and taste as Biobran/MGN-3, was given to control subjects at a dose of 500 mg everyday for 3 months |
- ILI incidence rate [ Time Frame: 12 weeks ]Incidence rate was calculated by dividing the number of incident ILI cases by the total number of the group participants during the 3 months study period.
- ILI incidence density [ Time Frame: 3600 Person-days ]incidence density was calculated by dividing the number of incident cases by the total person-time at risk
- NK cell activity [ Time Frame: 12 weeks ]Percentage of NK cells (CD56-positive CD3-negative) expressing CD-107a
- RIG-1, MDA5, ISG15, MX1 expression [ Time Frame: 72 hours ]Expression levels in BEAS-2B cells tissue culture exposed to Biobran/MGN-3
- Natural killer T-cells (NKT) cell activity [ Time Frame: 12 weeks ]Percentage of NK cells (CD56-positive CD3-positive) expressing CD-107a

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 56 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Ages of 56+ years
- Both sexes will be included.
- Local residents of Zagazig district
- Willing to participate in the study and give a written consent.
Exclusion Criteria:
- Subjects who took influenza vaccine, cortisone, or any other immunosuppressive agents such as radiation or chemotherapy.
- Diagnosed with infections or malignancies
- Presence of auto-immune disorders
- Marked portal hypertension, pancytopenia, renal, or kidney failure
- Presence of major psychological insult or under medication for psychological insult

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04646980
Egypt | |
Department of Community Medicine and Public Health, Faculty of Medicine, Zagazig University | |
Zagazig, Sharkia, Egypt, 44519 |
Principal Investigator: | Ahmed F Elsaid, MD/PhD | Department of Community Medicine and Public Health, Faculty of Medicine, Zagazig University |
Documents provided by Ahmed Farouk Elsaid, Zagazig University:
Responsible Party: | Ahmed Farouk Elsaid, Assistant Professor of Community Medicine and Public Health, Zagazig University |
ClinicalTrials.gov Identifier: | NCT04646980 |
Other Study ID Numbers: |
4034-12-6-2018 |
First Posted: | November 30, 2020 Key Record Dates |
Last Update Posted: | November 30, 2020 |
Last Verified: | November 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Plan Description: | Share results upon request. |
Supporting Materials: |
Study Protocol Statistical Analysis Plan (SAP) |
Time Frame: | Upon request |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Biobran/MGN-3 Old adults influenza-like illness |
NK cells activity Degranulation assay RIG-1, MDA5, ISG15, MX1 |
Influenza, Human Respiratory Tract Infections Infections Orthomyxoviridae Infections |
RNA Virus Infections Virus Diseases Respiratory Tract Diseases |