drugset / Trial / NCT01885208

Efficacy and Safety of Semaglutide Once-weekly Versus Exenatide ER 2.0 mg Once-weekly as add-on to 1-2 Oral Antidiabetic Drugs (OADs) in Subjects With Type 2 Diabetes

NCT01885208 ↗

Phase 3 Completed 813 enrolled Novo Nordisk A/S
RandomizedParallel-groupOpen-labelTreatment

Summary

This trial is conducted in Europe and North and South America. The aim of the trial is to investigate the efficacy and safety of semaglutide once-weekly versus exenatide ER (extended release) 2.0 mg once-weekly as add-on to 1-2 oral antidiabetic drugs (OADs) in subjects with type 2 diabetes.

Timeline

Start
2013-12-02
Primary completion
2015-07-13
Completion
2015-07-13

Outcome

Met primary endpoint

registry analysis (superiority test); Semaglutide 1.0 mg vs Exenatide ER 2.0 mg; p < 0.0001; Treatment difference -0.62 (95% CI -0.8 to -0.44); Mixed Models Analysis NCT01885208 ↗

paper Semaglutide 1.0 mg was superior to exenatide ER 2.0 mg in improving glycemic control and reducing body weight after 56 weeks of treatment; PMID 29246950 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Exenatide Peptide 2 mg Subcutaneous
Subject Semaglutide Peptide 1 mg Subcutaneous