drugset / Trial / NCT00915057

Effect of Chronic Viral Hepatitis on the Pharmacokinetics of NRL972.

NCT00915057

Phase 2 Completed 100 enrolled Norgine
Non-randomizedSingle-groupOpen-labelDiagnostic

Summary

Little is known about the nature and extent of the disturbance in hepatic function and biliary hepatic clearance in chronic viral hepatitis, while the course of this disease, the functional implications and response to treatment are difficult to predict. This study aims to assess this in patients with chronic viral hepatitis B (CHB) and chronic viral hepatitis C (CHC) who are eligible for treatment in accordance with the established consensus guidelines in the involved countries. The pharmacokinetics of NRL972 will be determined at baseline (within one month of starting treatment), at 3-monthly intervals during treatment, for up to 12 months (or at the end of treatment), and at 3 and 6 months after the end on treatment. This will provide a clearer understanding regarding the use of the pharmacokinetics of NRL972 in detecting changes in biliary clearance during and after treatment for CHB and CHC.

Timeline

Start
2009-03
Primary completion
2009-03
Completion
2009-03

Drugs

EvaluationDrugModalityDoseRoute
Subject FLUORESCEIN LISICOL Diagnostic / imaging agent 2 mg Intravenous

Indications