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BioFe, Medical Food for the Dietary Management of Iron Deficiency

Primary Purpose

Iron Deficiency

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
BioFe Medical Food
Sponsored by
Sidero Bioscience, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Iron Deficiency

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Moderate iron deficiency defined as transferrin saturation (TSAT) <20% and serum ferritin <50 ng/mL.

Exclusion Criteria:

  • Female subjects who are pregnant, plan to become pregnant, or not willing to use an acceptable form of contraception (tubal ligation or otherwise be incapable of pregnancy, hormonal contraceptives, spermicide plus barrier, or intrauterine device).
  • Female subjects who are breastfeeding or plan to breastfeed after enrolling in the study.
  • Hemochromatosis or other iron storage disorders.
  • Hemoglobin below 8 g/dL.
  • Previous gastric bypass, sleeve gastrectomy, or gastric band surgery.
  • Currently on iron supplements and/or multivitamins containing iron (subjects may be pre-screened four weeks prior to the screening visit in order to stop/washout or switch to vitamins not containing iron).
  • Currently on monoamine oxidase inhibitors (MAOIs) or Demerol.
  • Current diagnosis of asthma and is actively using anti-asthmatic therapy.
  • Smoking within two weeks of screening, current smoking, or anticipated smoking after enrolling in the study.
  • Active malignancy within one year of screening.
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) greater than two times the upper limit of normal.
  • Known positive Hepatitis B, Hepatitis C, or HIV-1/HIV-2.
  • Unregulated hypertension, chronic kidney disease, irritable bowel syndrome, anemia of chronic diseases, chronic autoimmune inflammatory condition.
  • Significant cardiovascular disease or congestive heart failure.
  • Known allergy to yeast or any other component of BioFe.
  • Received an investigational drug within 30 days of screening.
  • Any laboratory abnormality, medical condition or psychiatric disorder, which in the opinion of the clinical principal investigator or Sponsor, may result in the subject being unable to comply with study requirements.

Sites / Locations

  • Green & Seidner Family Practice Associates
  • Frontier Clinical Research, LLC
  • Frontier Clinical Research, LLC

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

BioFe Medical Food

Arm Description

Escalating consumption of BioFe in a single cohort of up to 40 subjects with iron deficiency.

Outcomes

Primary Outcome Measures

Safety and Tolerability as the number of participants with treatment-related adverse events as assessed by CTCAE v4.03
Blood cell, blood chemistry, and stool sample analysis. Health questionnaires including GI symptoms, fatigue, and quality of life by the Short Form 36 (SF-36) questionnaire

Secondary Outcome Measures

Correction of Iron Deficiency
Increase in Serum Iron Measurements Ferritin, Iron, And TSAT

Full Information

First Posted
June 26, 2017
Last Updated
June 30, 2020
Sponsor
Sidero Bioscience, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03210168
Brief Title
BioFe, Medical Food for the Dietary Management of Iron Deficiency
Official Title
A Clinical Trial of BioFe, Medical Food for the Dietary Management of Iron Deficiency
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
July 4, 2017 (Actual)
Primary Completion Date
December 18, 2017 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidero Bioscience, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluates the safety, tolerability, and activity of BioFe in the dietary management of iron deficiency in adults.
Detailed Description
Iron deficiency is the most common, widespread, and costly nutritional disorder worldwide with the World Health Organization (WHO) stating that up to 2 billion people are iron deficient. There is a serious and widespread misconception that oral iron supplements are safe and effective at alleviating iron deficiency. In a recent Cochrane review of 67 clinical trials, women taking oral iron supplements had a mere 38% decreased risk of iron deficiency compared to placebo. On the contrary, these subjects had a 114% increased risk of side effects, the vast majority of which were associated with gastrointestinal (GI) disturbance. In infants and children, iron deficiency impedes mental, motor, and auditory neuronal development leading to serious lifelong cognitive and physical deficiencies. In adults, iron deficiency, and associated iron deficiency anemia, cause extreme fatigue, decreased immune system function and increased susceptibility to infectious disease, reduced work capacity, dizziness, headaches, hair loss, and generalized reduced quality of life. Iron deficiency is also linked to Restless Leg Syndrome (RLS), adult hearing deficits, reduced strength, coordination, and endurance, anxiety, increased heart failure morbidity, decreased intellectual performance, and erectile dysfunction among many others conditions. Most iron deficient people are not effectively treated by, or are intolerant to, oral iron supplements. Intravenous iron repletion drugs effective, but are also costly and onerous to deliver leading to both patient and payor dissatisfaction. BioFe, Medical Food for Iron Deficiency is nutritional/Baker's yeast (Saccharomyces cerevisiae), expressing the Ferritin protein. Ferritin is an indispensable iron storage, transport and absorption protein normally produced at low levels by almost all living organisms. An illustrative example of the biology of the Ferritin/Iron complex is its presence in human breast milk, providing infants the natural biological iron required for rapid learning and development, without gastrointestinal upset. BioFe provides high level expression of Ferritin that is naturally complexed with iron during culture, is pasteurized, and dried.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Escalating consumption of BioFe in a single cohort of up to 40 subjects with iron deficiency.
Masking
None (Open Label)
Allocation
N/A
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BioFe Medical Food
Arm Type
Experimental
Arm Description
Escalating consumption of BioFe in a single cohort of up to 40 subjects with iron deficiency.
Intervention Type
Other
Intervention Name(s)
BioFe Medical Food
Intervention Description
BioFe is comprised of cultured nutritional/Baker's yeast (Saccharomyces cerevisiae) with high levels of Ferritin/Iron complex, pasteurized, and dried
Primary Outcome Measure Information:
Title
Safety and Tolerability as the number of participants with treatment-related adverse events as assessed by CTCAE v4.03
Description
Blood cell, blood chemistry, and stool sample analysis. Health questionnaires including GI symptoms, fatigue, and quality of life by the Short Form 36 (SF-36) questionnaire
Time Frame
10 Weeks
Secondary Outcome Measure Information:
Title
Correction of Iron Deficiency
Description
Increase in Serum Iron Measurements Ferritin, Iron, And TSAT
Time Frame
10 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Moderate iron deficiency defined as transferrin saturation (TSAT) <20% and serum ferritin <50 ng/mL. Exclusion Criteria: Female subjects who are pregnant, plan to become pregnant, or not willing to use an acceptable form of contraception (tubal ligation or otherwise be incapable of pregnancy, hormonal contraceptives, spermicide plus barrier, or intrauterine device). Female subjects who are breastfeeding or plan to breastfeed after enrolling in the study. Hemochromatosis or other iron storage disorders. Hemoglobin below 8 g/dL. Previous gastric bypass, sleeve gastrectomy, or gastric band surgery. Currently on iron supplements and/or multivitamins containing iron (subjects may be pre-screened four weeks prior to the screening visit in order to stop/washout or switch to vitamins not containing iron). Currently on monoamine oxidase inhibitors (MAOIs) or Demerol. Current diagnosis of asthma and is actively using anti-asthmatic therapy. Smoking within two weeks of screening, current smoking, or anticipated smoking after enrolling in the study. Active malignancy within one year of screening. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) greater than two times the upper limit of normal. Known positive Hepatitis B, Hepatitis C, or HIV-1/HIV-2. Unregulated hypertension, chronic kidney disease, irritable bowel syndrome, anemia of chronic diseases, chronic autoimmune inflammatory condition. Significant cardiovascular disease or congestive heart failure. Known allergy to yeast or any other component of BioFe. Received an investigational drug within 30 days of screening. Any laboratory abnormality, medical condition or psychiatric disorder, which in the opinion of the clinical principal investigator or Sponsor, may result in the subject being unable to comply with study requirements.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Connor, PhD
Organizational Affiliation
Chairman and Co-Founder
Official's Role
Study Director
Facility Information:
Facility Name
Green & Seidner Family Practice Associates
City
Lansdale
State/Province
Pennsylvania
ZIP/Postal Code
19446
Country
United States
Facility Name
Frontier Clinical Research, LLC
City
Scottdale
State/Province
Pennsylvania
ZIP/Postal Code
15683
Country
United States
Facility Name
Frontier Clinical Research, LLC
City
Smithfield
State/Province
Pennsylvania
ZIP/Postal Code
15478
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

BioFe, Medical Food for the Dietary Management of Iron Deficiency

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