Phase 2 Reduction of Dietary Mycotoxin Exposure by ACCS100" (RDMEACCS100)

This study has been completed.
Sponsor:
Collaborators:
Texas A&M University
University of Georgia
The University of Texas at San Antonio
Information provided by (Responsible Party):
Texas Enterosorbents Incorporated
ClinicalTrials.gov Identifier:
NCT01677195
First received: August 29, 2012
Last updated: December 14, 2015
Last verified: December 2015
  Purpose

The primary purpose of the study is to evaluate the effectiveness of a naturally occurring clay substance (ACCS100) in reducing harmful effects of aflatoxin exposure (a carcinogen) and fumonisin (a cancer promoter). This clay substance contains of a variety of minerals including calcium, sodium, potassium, and magnesium. UPSN and similar aluminosilicate minerals have been regularly used as dietary supplements by humans and animals, and the safety of this naturally occurring clay substance has been tested in clinical trials. The FDA treats such minerals or nutritional supplements as a drug when tested for potential of lessening the likelihood of disease (i.e., potential for mitigating disease).

This study involves the use of an investigational drug called Hydrated Sodium Calcium Aluminosilicate (ACCS100). "Investigational" means that the "drug" has not yet been approved by the U.S. Food & Drug Administration (FDA) for reducing harmful effects mycotoxin exposure in humans.


Condition Intervention Phase
Dietary Carcinogenesis
Drug: ACCS100
Drug: Placebo
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Prevention
Official Title: "Phase II, Reduction of Dietary Mycotoxin Exposure in Persons in Bexar County, Texas by Ingestion of ACCS100 Capsules Compared to Placebo."

Resource links provided by NLM:


Further study details as provided by Texas Enterosorbents Incorporated:

Primary Outcome Measures:
  • AFB1-lysine Adduct (pg/mg) Overtime [ Time Frame: 3 months on intervention (weeks 0-12); 1 month off intervention (week 16) ] [ Designated as safety issue: No ]
    After randomization, participants provided serum samples at baseline, weeks 4, 12, and 16. Week 16 represents one month off treatment.


Enrollment: 234
Study Start Date: September 2012
Study Completion Date: August 2014
Primary Completion Date: August 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: ACCS100 High Dose
Participants will receive a total daily dose of 3 grams of ACCS100; 1 gram three times a day with meals.
Drug: ACCS100
ACCS100 is not absorbed. The dose is estimated based on the volume of the gastrointestinal tract. We estimate that the average human intestinal tract has a volume of approximately 4 liters. In the high dose group, the effective concentration in the gut is 0.75 milligrams per milliliter. In the low dose, the effective concentration in the gut is 0.375 milligrams per milliliter. The test article is made by filling gelatin capsules with 500 milligrams of ACCS100. There are no excipients used in the manufacturing process of the test article.
Other Names:
  • HSCAS
  • UPSN
  • NS
Active Comparator: ACCS100 Low Dose
Participants will receive a total daily dose of 1.5 grams of ACCS100; 500 mgs three times a day with meals.
Drug: ACCS100
ACCS100 is not absorbed. The dose is estimated based on the volume of the gastrointestinal tract. We estimate that the average human intestinal tract has a volume of approximately 4 liters. In the high dose group, the effective concentration in the gut is 0.75 milligrams per milliliter. In the low dose, the effective concentration in the gut is 0.375 milligrams per milliliter. The test article is made by filling gelatin capsules with 500 milligrams of ACCS100. There are no excipients used in the manufacturing process of the test article.
Other Names:
  • HSCAS
  • UPSN
  • NS
Placebo Comparator: Placebo
Participants will receive placebo capsules shown not to absorb mycotoxins three times a day with meals.
Drug: Placebo
Placebo is calcium carbonate, USP. This calcium mineral does not absorb mycotoxins, specifically aflatoxin and fumonisin. This mineral has approximately the same physical appearance as active test article.
Other Name: Calcium Carbonate

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

3.1 Participant Inclusion Criteria 3.1.1 Detectable blood AFB1-albumin adduct levels (limit of detection=0.01 pmol/mg albumin) 3.1.2 18 -85 years 3.1.3 Ability to take oral capsules 3.1.4 Negative urine pregnancy test for women of childbearing age 3.1.5 Must have the ability to understand and the willingness to provide a written informed consent to participate in the study

Exclusion Criteria:

3.2 Participant Exclusion Criteria 3.2.1 History of known allergy to silicates 3.2.2 Pregnancy or lactation 3.2.3 History of significant neurological or psychiatric disorders that would impede giving consent, treatment, or follow up 3.2.4 Any serious systemic disorders incompatible with the study 3.2.5 History of chronic disease (ie heart disease, renal disease). A participant may have a diagnosis of and be managed for diabetes) Any recent diagnosis of cancer.

3.2.6 Participation in any other clinical study where the participant is actively taking an investigational medication within the last 30 days

  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01677195

Locations
United States, Texas
University of Texas Health Science Center Cancer Therapy and Research Center
San Antonio, Texas, United States, 78229
Sponsors and Collaborators
Texas Enterosorbents Incorporated
Texas A&M University
University of Georgia
The University of Texas at San Antonio
Investigators
Principal Investigator: Bradley H Pollock, MPH, Ph.D. University of Texas Health Science Center San Antonio Texas
  More Information

Publications:
Responsible Party: Texas Enterosorbents Incorporated
ClinicalTrials.gov Identifier: NCT01677195     History of Changes
Other Study ID Numbers: TxESI 12-001 
Study First Received: August 29, 2012
Results First Received: December 14, 2015
Last Updated: December 14, 2015
Health Authority: United States: Food and Drug Administration

Keywords provided by Texas Enterosorbents Incorporated:
Mycotoxins
Aflatoxin
Fumonisin
Aflatoxicosis
Dietary
Cancer

Additional relevant MeSH terms:
Carcinogenesis
Neoplasms
Neoplastic Processes
Pathologic Processes
Calcium Carbonate
Antacids
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions

ClinicalTrials.gov processed this record on February 04, 2016