drugset / Trial / NCT01713530

A 26-week Trial Comparing Efficacy and Safety of Insulin Degludec/Insulin Aspart BID and Insulin Degludec OD Plus Insulin Aspart in Subjects With Type 2 Diabetes Mellitus Treated With Basal Insulin in Need of Treatment Intensification With Mealtime Insulin

NCT01713530 ↗

Phase 3 Completed 274 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Africa, Europe and the United States of America (USA). The aim of the trial is to compare the difference in change in glycosylated haemoglobin (HbA1c) between insulin degludec/insulin aspart (IDegAsp) and/or oral anti-diabetic drugs (OADs) and insulin degludec (IDeg) plus insulin aspart (IAsp)and/or OADs.

Timeline

Start
2013-02-21
Primary completion
2014-01-09
Completion
2014-01-09

Outcome

Missed primary endpoint

paper The non-inferiority of IDegAsp versus IDeg+IAsp was not confirmed for mean change in HbA1c PMID 26592732 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject insulin aspart Protein / enzyme biologic — Subcutaneous
Subject insulin degludec Protein / enzyme biologic — Subcutaneous
Subject insulin degludec/insulin aspart Unknown — Subcutaneous