drugset / Trial / NCT01136928

Pharmacokinetic Interaction Study of Efavirenz and American Ginseng in Healthy Volunteers

NCT01136928

NaSingle-groupOpen-labelOther

Summary

This is a 4-week sequential drug interaction study to measure the effects of American ginseng on efavirenz pharmacokinetics using steady-state 24-hour Area Under the Curve (AUC) and Cmax as the primary comparison measures in healthy male volunteers. Efavirenz Cmin, T1/2, tmax, and clearance will also be assessed as secondary outcome measures. This study is a phase I, prospective, within-subject, fixed-order, two-period, multiple dose, open label, drug interaction study, to determine the stead-state plasma pharmacokinetic profile of efavirenz before and after concurrent treatment with American ginseng. The investigators hypothesis is that concurrent oral administration of American ginseng for up to 14 days will not significantly alter the steady-state plasma pharmacokinetic of efavirenz.

Timeline

Start
2010-09-28
Primary completion
2011-03-14
Completion
2011-03-14

Drugs

EvaluationDrugModalityDoseRoute
Subject American ginseng Unknown 3000 mg Oral
Subject Efavirenz Other / unclassified 600 mg Oral

Indications

No indication recorded.