drugset / Trial / NCT01365507

Efficacy and Safety of Insulin Degludec/Insulin Aspart in Insulin-naïve Subjects With Type 2 Diabetes Using Two Dosing Regimens

NCT01365507 ↗

Phase 3 Completed 276 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Asia and North America. The aim of this trial is to compare the efficacy and safety of insulin degludec/insulin aspart (IDegAsp) once daily in insulin-naïve subjects with type 2 diabetes mellitus when using two different titration algorithms (dose individually adjusted) as add-on to subject's ongoing treatment with metformin.

Timeline

Start
2011-06
Primary completion
2012-04
Completion
2012-04

Outcome

Met primary endpoint

paper confirming the non-inferiority of IDegAspSimple to IDegAspStepwise PMID 26773557 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject insulin degludec/insulin aspart Unknown — Subcutaneous