Safety and Pharmacokinetic Study of BIO 300 Capsules

NCT ID: NCT00504335

Last Updated: 2015-03-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-06-30
• Study Completion Date: 2007-10-31

Brief Summary

This trial is designed to evaluate the safety and pharmacokinetics of BIO 300 capsules when administered orally to healthy male and female volunteers. BIO 300 is expected to be safe for use starting at 500 mg.

Detailed Description

This clinical trial will assess the safety and PK of BIO 300 capsules at doses expected to deliver a radioprotective or therapeutic effect in humans. Humanetics is planning to conduct this Phase I, single dose, dose-escalation (500, 1000, 1500, and 2000 milligrams) study of the safety, tolerability and pharmacokinetics of BIO 300 by recruiting approximately 24 healthy men and women between the ages of 18 and 64 to be enrolled in cohorts of 6 subjects per group. The first cohort will receive one 500 mg BIO 300 capsule and pharmacokinetic blood sampling will be conducted over the first 4 days in an outpatient setting at a clinic skilled in this type of Phase I trial. Blood samples will be analyzed for BIO 300 levels, hematology, chemistry, lipid profiles, phosphorus, clotting factors and fibrinogen as well as pancreatic lipase and amylase. Urinalysis will assess kidney function as well as creatinine clearance and BIO 300 clearance. All subjects will be monitored for adverse events and the safety of BIO 300 capsules will be evaluated in this setting. After review of all safety information and provided no clinically significant negative findings are revealed, the second cohort will be treated with 1000mg BIO 300 (two 500mg capsules) using the same PK sampling program. Again safety concerns will be reviewed and provided no clinically significant negative findings are revealed, the third and fourth cohort will be treated with 1500 and 2000 mg, respectively, of BIO 300 using the same PK sampling program.

Conditions

Acute Radiation Syndrome

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

500 BIO 300 capsule

The first cohort will receive one 500 BIO 300 capsule and pharmacokinetic blood sampling will be conducted over the first 4 days in an outpatient setting

Group Type: EXPERIMENTAL

BIO 300 Capsules

Intervention Type: DRUG

1000 BIO 300 capsule

the second cohort will be treated with 1000 mg BIO 300 using the same PK sampling program

Group Type: EXPERIMENTAL

BIO 300 Capsules

Intervention Type: DRUG

1500 BIO 300 capsule

the third cohort will be treated with 1500 mg BIO 300using the same PK sampling program

Group Type: EXPERIMENTAL

BIO 300 Capsules

Intervention Type: DRUG

2000 BIO 300 capsule

the forth cohort will be treated with 2000 mg BIO 300using the same PK sampling program

Group Type: EXPERIMENTAL

BIO 300 Capsules

Intervention Type: DRUG

Interventions

BIO 300 Capsules

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Healthy male and female subjects, age 18-64, who have signed the consent form

• Subjects with a body mass index (BMI) 18-30 kg/m2
• Subjects who are willing to abstain from sex or use a barrier method of birth control (Women 1 week, Men 4 months after leaving the trial)
• Subjects with a negative pregnancy test and drug screen
• Subjects with laboratory values within normal limits (CBC/differential, CMP, enzymes, ECG, vital signs, urinalysis)
• Subjects with ability to comprehend and complete the questionnaires and forms
• Subjects who are likely to comply with study procedures and test article consumption
• Subjects whose schedules permit a 10-12 hour stay in the clinic followed by daily evaluations for one week (7 days)
• Subjects who are available for a 14-day follow up phone call (women) and 4-month follow up phone call (men).
• Subjects who are likely to abstain from taking unauthorized medications or supplements or participating in any other clinical trial or experimental treatment during this trial
• Subjects who are likely to follow the low isoflavone diet program

Exclusion Criteria

• · Subjects with any allergic reaction or sensitivity to soy, isoflavones, or any component of the test article product

• Subjects who consume >5 alcoholic beverages per week
• Subjects who are pregnant, lactating, or at risk of becoming pregnant
• Subjects who have blood (or urine) levels outside the normal range for any of the hepatic, renal, hematologic, lipid or coagulation parameters measured.
• Subjects on Hormone Replacement Therapy or Birth Control Pills within the past three months.
• Subjects on any other clinical trial or experimental treatment in the past 3 months
• Subjects with a history of diabetes (Type 1 or Type 2 diabetes mellitus) or other endocrine disorders, uncontrolled hypertension, prior cerebrovascular accident or seizure disorder, cardiovascular, hepatic or renal disease, active cancer, hematologic disorder, thromboembolic disease, or HIV infection.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

United States Department of Defense

FED

Sponsor Role: collaborator

Humanetics Corporation

INDUSTRY

Sponsor Role: lead

Principal Investigators

John L Zenk, MD

Role: PRINCIPAL_INVESTIGATOR

Humanetics Corporation

Other Identifiers

MARC006-025

Identifier Type: -

Identifier Source: org_study_id