Safety and Pharmacokinetic Study of BIO 300 Capsules

Humanetics Corporation24 enrolled

Overview

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.

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.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Acute Radiation Syndrome

Interventions

BIO 300 CapsulesDRUG

Eligibility

Sex: ALLMin age: 18 YearsMax age: 64 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Outcomes

Primary Outcomes

Safety as assessed by lab work and adverse event monitoring

Time frame: 1 month for females & 4 months for males

Secondary Outcomes

Pharmacokinetic assessment by analyzing patient serum for free and total BIO 300 content at multiple time points.

Time frame: 7 days

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.