Healthy volunteers
Conditions
Interventions
For in vitro assay, participants are taken a blood sampling under an overnight fasting. As to a clinical trial, on the day 1, subjects are administered single 10 mg of simvastatin orally, and undergo
Sponsors
Fukushima Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy adults
Exclusion criteria
Exclusion criteria: Smoker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum paraoxonase-3 activity Serum paraoxonase-3 concentration Plasma concentrations of simvastatin Plasma concentrations of midazolam | — |
Countries
Japan
Contacts
Public ContactShingen Misaka
Fukushima Medical University School of Medicine, Department of Pharmacology
Outcome results
None listed