drugset / Trial / NCT01850615

Efficacy and Safety of FIAsp in a Basal-bolus Regimen Versus Basal Insulin Therapy, Both in Combination With Metformin in Adult Subjects With Type 2 Diabetes

NCT01850615 ↗

Phase 3 Completed 323 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Asia, Europe, South America, and the United States of America (USA). The aim of the trial is to investigate efficacy and safety of FIAsp in a basal-bolus regimen versus basal insulin therapy, both in combination with metformin in adult subjects with type 2 diabetes.

Timeline

Start
2013-09-23
Primary completion
2014-11-17
Completion
2014-11-17

Outcome

Met primary endpoint

paper estimated treatment difference [95% confidence interval] -0.94% [-1.17; -0.72]; -10.3 mmol/mol [-12.8; -7.8]; P  < .0001. PMID 28345792 ↗

paper CONCLUSIONS: In T2D, faster aspart in a BB regimen provided superior glycaemic control as compared with basal-only insulin PMID 28345792 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Faster-acting insulin aspart Unknown — Subcutaneous
Background insulin detemir Protein / enzyme biologic — Subcutaneous
Background insulin glargine Protein / enzyme biologic — Subcutaneous
Background regular insulin Protein / enzyme biologic — Subcutaneous