A Trial Investigating the Relationship Between Pharmacodynamic and Interstitial Concentration for Insulin Detemir and Human Insulin

• Status: Completed
• Trial end date: 1999-12-01
• Target enrollment: 0
• Participant gender: Male

Summary

This study is conducted in Europe. The aim of this study is to estimate the relationship between pharmacodynamic and interstitial pharmacokinetic steady state following intravenous (i.v.) administration of insulin detemir and human soluble insulin.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Novo Nordisk A/S
• Treatments: Insulin; Insulin Detemir; Insulin, Globin Zinc

Criteria

Inclusion Criteria:

• Healthy males between 19 and 50 years inclusive

• The subject must give signed informed consent before any trial related activity. (Trial related activities are any procedures that would not have been performed during the normal management of the subject)

• Body Mass Index (BMI) below 27 kg/m^2

• Fasting blood glucose maximum 6 mmol/l

Exclusion Criteria:

• Participation in any other clinical trial involving other investigational products within the last 3 months