drugset / Trial / NCT01562561

Efficacy and Safety of Repaglinide Combined With Insulin NPH in Subjects With Type 2 Diabetes

NCT01562561

Phase 3 Completed 213 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Asia and South Africa. The aim of this trial is to compare the efficacy and safety of repaglinide plus insulin NPH (insulin Neutral Protamine Hagedorn) with insulin NPH alone in subjects with type 2 diabetes inadequately controlled on repaglinide.

Timeline

Start
2001-06-01
Primary completion
2002-12-20
Completion
2002-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Repaglinide Small molecule 2 mg
Subject insulin NPH Protein / enzyme biologic Subcutaneous