drugset / Trial / NCT00768209

A Study to Evaluate the Pharmacokinetics of VI-0521 in Subjects With Hepatic Impairment

NCT00768209

Phase 1 Completed 18 enrolled VIVUS LLC Covance · collabSentrx · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study is designed to determine the effects of a single dose of the study medication in subjects with and without hepatic impairment. 18 to 24 subjects will participate by having multiple blood draws taken to measure the level of study medication in their blood over time.

Timeline

Start
2008-10
Primary completion
2009-03
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Phentermine Small molecule 15 mg Oral
Subject Topiramate Small molecule 92 mg Oral

Indications

No indication recorded.