Overview

Drug-Drug Interaction Study Between Fenofibric Acid and Efavirenz

Status:
Completed
Trial end date:
2008-03-01
Target enrollment:
0
Participant gender:
All
Summary
Efavirenz is predominantly metabolized by cytochrome P450 (CYP) 2B6. Fenofibric Acid is an inhibitor of CYP 2B6. This study will evaluate the effect of multiple doses of fenofibric acid at steady-state on the pharmacokinetics of single-dose efavirenz in healthy adult subjects.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Mutual Pharmaceutical Company, Inc.
Treatments:
Efavirenz
Fenofibrate
Fenofibric acid
Criteria
Inclusion Criteria:

- Healthy adults 18-45 years of age

- Non-smoking

- Non-pregnant (post-menopausal, surgically sterile or using effective contraceptive
measures)

- Body mass index (BMI) less than 30

- Medically healthy on the basis of medical history and physical examination

- Hemoglobin > or = to 12g/dL

- Completion of the screening process within 28 days prior to dosing

- Provision of voluntary written informed consent

Exclusion Criteria:

- Recent participation (within 28 days) in other research studies

- Recent significant blood donation or plasma donation

- Pregnant or lactating

- Test positive at screening for human immunodeficiency virus (HIV), hepatitis B surface
antigen (HbsAg), or hepatitis C virus (HCV)

- Recent (2-year) history or evidence of alcoholism or drug abuse

- History or presence of significant cardiovascular, pulmonary, hepatic, gallbladder or
biliary tract, renal, hematologic, gastrointestinal, endocrine, immunologic,
dermatologic, neurologic, or psychiatric disease

- Subjects who have used any drugs or substances known to inhibit or induce cytochrome
(CYP) P450 enzymes and/or P-glycoprotein (P-gp) within 28 days prior to the first dose
and throughout the study

- Drug allergies to fenofibric acid or efavirenz