drugset / Trial / NCT00746499

Pharmacokinetic Study of Raltegravir in Healthy Premenopausal Women.

NCT00746499

Phase 1 Completed 7 enrolled University of North Carolina, Chapel Hill
NaSingle-groupOpen-label

Summary

Healthy subjects will take study drug by mouth twice a day for 7 consecutive days, blood and cervicovaginal samples will be taken most mornings around the AM dose. Two visits, \~14 hrs in length will be required on Day 1 and 7. The purpose of this study is to measure how much raltegravir is found in the genital tract after taking it orally.

Timeline

Start
2008-09
Primary completion
2008-11
Completion
2008-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Raltegravir Other / unclassified 400 mg Oral

Indications

No indication recorded.