drugset / Trial / NCT01507389

Safety of Liraglutide in Subjects With Liver Impairment and in Subjects With Normal Liver Function

NCT01507389

Phase 1 Completed 24 enrolled Novo Nordisk A/S
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Europe. The aim of this trial is to investigate liraglutide in subjects with mild, moderate and severe degrees of hepatic impairment compared with subjects with normal hepatic function.

Timeline

Start
2006-03
Primary completion
2006-06
Completion
2006-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Liraglutide Peptide 0.75 mg Subcutaneous