drugset / Trial / NCT00621881

A Phase 1 Study to Compare the PK and Safety of Naproxcinod in Hepatic Impaired Patients and Matching Healthy Subjects

NCT00621881

Phase 1 Completed 24 enrolled NicOx
Non-randomizedParallel-groupOpen-labelBasic science

Summary

This is an open-label study that will compare the pharmacokinetic and safety effects of naproxcinod in hepatic impaired patients vs. matching healthy subjects.

Timeline

Start
2008-01
Primary completion
2008-04
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject naproxcinod Other / unclassified 750 mg

Indications