drugset / Trial / NCT01507272

Safety and Tolerability of Liraglutide in Healthy Male Volunteers

NCT01507272

Phase 1 Completed 34 enrolled Novo Nordisk A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is conducted in Europe. The aim of this trial is to assess the safety and tolerability (maximum tolerated dose) after five ascending single doses of NNC 90-1170 (liraglutide).

Timeline

Start
1999-03
Primary completion
1999-12
Completion
1999-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Liraglutide Peptide 1.25 ug/kg Subcutaneous
Subject Liraglutide Peptide 2.5 ug/kg Subcutaneous
Subject Liraglutide Peptide 5 ug/kg Subcutaneous
Subject Liraglutide Peptide 10 ug/kg Subcutaneous
Subject Liraglutide Peptide 20 ug/kg Subcutaneous

Indications