drugset / Trial / NCT01680341

Comparison of the Efficacy and Safety of Two Different Dose Adjustment Regimens for Insulin Degludec/Insulin Aspart in Subjects With Type 2 Diabetes Mellitus Previously Treated With Insulin Glargine

NCT01680341 ↗

Phase 3 Completed 272 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Africa, Asia, Europe and the United States of America (USA). The aim of the trial is to compare the efficacy and safety of two different titration algorithms for insulin degludec/insulin aspart (IDeg/IAsp) in subjects with type 2 diabetes mellitus previously treated with insulin glargine.

Timeline

Start
2012-08-31
Primary completion
2013-08-22
Completion
2013-08-22

Outcome

Met primary endpoint

paper mean change from baseline in glycated hemoglobin (HbA1c) with IDegAsp[BIDSimple] was noninferior to IDegAsp[BIDStep-wise] PMID 26720250 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject insulin degludec/insulin aspart Unknown — Subcutaneous