Cytochrome P450 CYP3A5 Enzyme Polymorphism, Healthy Subjects, Pharmacokinetics of Maraviroc
Conditions
Keywords
CYP3A5, maraviroc, polymorphism
Brief summary
The purpose of this study is to evaluate the influence of genetic polymorphism of cytochrome P450 3A5 on pharmacokinetics of maraviroc and its oxidative metabolites
Detailed description
This study aims to evaluate the effects of CYP3A5 genotype on pharmacokinetics of maraviroc and its oxidative metabolites. A single oral dose of 300 mg maraviroc will be given to 24 eligible healthy individuals who will be screened and determined to have specific CYP3A5 genotype - 8 homozygous wild type (2 CYP3A5\*1 alleles), 8 heterozygous (1 CYP3A5\*1 allele and 1 mutant allele), and 8 without wild type genotype (2 mutant alleles). Blood samples will be drawn and urine samples will be collected immediately before and during a 32-hr period following the dose. The concentrations of maraviroc and its oxidative metabolites from the blood and urine samples will be measured and the pharmacokinetics of maraviroc and its metabolites will be compared among the three groups with different CYP3A5 polymorphic status. \--------------------------------------------------------------------------------
Interventions
DRUGMaraviroc
Sponsors
Johns Hopkins University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy with no acute medical illness * Willing to provide written informed consent * Age 18-65 years * Negative serum pregnancy test (females only) at screening and a negative urine pregnancy test (females only) on day of dosing * HIV seronegative at screening, as determined by any licensed ELISA * At screening, no evidence of hepatic or renal impairment (LFT's \< 1.5 Upper Limit of Normal (ULN), creatinine clearance \> than 60 ml/min, total bilirubin below ULN, AST and ALT below 1.5 ULN) * 8 subjects with homozygous CYP3A5 allele \*1 (wild type) * 8 subjects with 1 CYP3A5\*1 allele and 1 mutant allele * 8 subjects with CYP3A5 allele other than \*1
Exclusion criteria
* Concomitant medication (prescription or over-the-counter) or herbal supplements for which there is a known risk of pharmacokinetic or pharmacodynamic drug interactions, including those that inhibit CYP3A4 as listed on the P450 Drug Interaction Table (http://medicine.iupui.edu/clinpharm/ddis/table.aspx) * History of postural hypotension or cardiovascular disease * Active medical or psychological condition that, in the opinion of the investigator, might put the volunteer at undue risk or interfere with the participation of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Area under the plasma concentration-time curve | 0-32 hour post dose administration |
Secondary
| Measure | Time frame |
|---|---|
| Clearance | 0-32 hr post dose administration |
| Plasma peak concentration | 0-32 hr post dose administration |
| Plasma half-life | 0-32 hr post dose administration |
| Urinary metabolic ratio | 0-32 hr post dose administration |
Countries
United States
Outcome results
None listed