drugset / Trial / NCT02220296

A Trial Investigating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneous NNC0123-0338 in Healthy Subjects and in Subjects With Type 1 Diabetes Mellitus

NCT02220296

Phase 1 Completed 62 enrolled Novo Nordisk A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is conducted in Europe. The purpose is to evaluate safety and tolerability of a range of single doses of subcutaneous insulin 338.

Timeline

Start
2014-08-20
Primary completion
2015-03-31
Completion
2015-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject insulin 338 Protein / enzyme biologic Subcutaneous
Comparator insulin glargine Protein / enzyme biologic 0.4 iu/kg Subcutaneous