Exenatide once weekly versus liraglutide once daily in patients with type 2 diabetes (DURATION-6): a randomised, open-label study
Summary Background Glucagon-like peptide-1 receptor agonists exenatide and liraglutide have been shown to improve glycaemic control and reduce bodyweight in patients with type 2 diabetes. We compared the efficacy and safety of exenatide once weekly with liraglutide once daily in patients with type 2...
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Veröffentlicht in: | The Lancet (British edition) 2013-01, Vol.381 (9861), p.117-124 |
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Sprache: | eng |
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Zusammenfassung: | Summary Background Glucagon-like peptide-1 receptor agonists exenatide and liraglutide have been shown to improve glycaemic control and reduce bodyweight in patients with type 2 diabetes. We compared the efficacy and safety of exenatide once weekly with liraglutide once daily in patients with type 2 diabetes. Methods We did a 26 week, open-label, randomised, parallel-group study at 105 sites in 19 countries between Jan 11, 2010, and Jan 17, 2011. Patients aged 18 years or older with type 2 diabetes treated with lifestyle modification and oral antihyperglycaemic drugs were randomly assigned (1:1), via a computer-generated randomisation sequence with a voice response system, to receive injections of once-daily liraglutide (1·8 mg) or once-weekly exenatide (2 mg). Participants and investigators were not masked to treatment assignment. The primary endpoint was change in glycated haemoglobin (HbA1c ) from baseline to week 26. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov , number NCT01029886. Findings Of 912 randomised patients, 911 were included in the intention-to-treat analysis (450 liraglutide, 461 exenatide). The least-squares mean change in HbA1c was greater in patients in the liraglutide group (−1·48%, SE 0·05; n=386) than in those in the exenatide group (–1·28%, 0·05; 390) with the treatment difference (0·21%, 95% CI 0·08–0·33) not meeting predefined non-inferiority criteria (upper limit of CI |
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ISSN: | 0140-6736 1474-547X |
DOI: | 10.1016/S0140-6736(12)61267-7 |