The Efficacy of IDegLira (Insulin Degludec/Liraglutide Combination) in Adults with Type 2 Diabetes Inadequately Controlled with a GLP-1 Receptor Agonist and Oral Therapy: DUAL III Randomized Clinical Trial.
Diabetes Ther · 2017
Last updated 2026-05-28In a 26-week study of 438 adults with type 2 diabetes not well-controlled on a GLP-1 drug and other medications, switching to IDegLira (a combination of insulin degludec and liraglutide) reduced blood sugar control (HbA1c) from 7.8% to 6.4%, compared to a reduction from 7.7% to 7.4% for those who stayed on their original GLP-1 drug. About 75% of those on IDegLira reached a blood sugar target of less than 7%, versus 36% on the original treatment. Weight increased by 2.0 kg with IDegLira but decreased by 0.8 kg with the original treatment.
AI summary of the abstract below.
| Journal | Diabetes Ther, 2017 |
|---|---|
| Citations | 117 |
| Relative citation ratio | 4.25 |
| NIH percentile | 90 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
INTRODUCTION: The progressive nature of type 2 diabetes necessitates treatment intensification. This often involves intensification with oral antidiabetic drugs (OADs) initially, followed by other agents, such as glucagon-like peptide-1 receptor agonists (GLP-1RAs), with the majority of patients eventually requiring insulin therapy. Therefore, this trial aimed to investigate the efficacy of IDegLira (combination of insulin degludec and liraglutide) in controlling glycemia in adults with type 2 diabetes who were inadequately controlled on a GLP-1RA and OADs.
METHODS: In this 26-week open-label phase 3b trial, patients on maximum-dose GLP-1RA therapy (liraglutide once daily or exenatide twice daily) with metformin alone or with pioglitazone and/or sulfonylurea were randomized 2:1 to IDegLira once daily (n = 292) or to unchanged GLP-1RA therapy (n = 146), continuing OADs at the pre-trial dose.
RESULTS: After 26 weeks, HbA reductions were superior with IDegLira versus unchanged GLP-1RA; estimated treatment difference -0.94% (-10.3 mmol/mol), p < 0.001. Mean HbA reduced from 7.8% to 6.4% (61.5 to 46.9 mmol/mol) with IDegLira and from 7.7 to 7.4% (60.8 to 57.1 mmol/mol) with unchanged GLP-1RA. With IDegLira, 75% and 63% of patients achieved HbA <7% and ≤6.5%, compared with 36% and 23% on unchanged GLP-1RA, respectively. Fasting plasma glucose and 9-point self-monitored blood glucose profiles improved significantly more with IDegLira versus unchanged GLP-1RA. The mean change in weight was +2.0 kg with IDegLira, versus -0.8 kg with unchanged GLP-1RA. Rates of confirmed hypoglycemia were low, but higher with IDegLira versus unchanged GLP-1RA. The safety profile of IDegLira was consistent with previous findings; both treatments were well tolerated and the rate of nausea was low in both groups. IDegLira improved patient-reported outcomes versus unchanged GLP-1RA.
CONCLUSIONS: IDegLira provided superior glycemic control versus unchanged GLP-1RA and represents an efficacious intensification approach in patients inadequately controlled on GLP-1RAs.
TRIAL REGISTRATION: ClinicalTrials.gov #NCT01676116.
FUNDING: Novo Nordisk.
Verbatim abstract via PubMed 27943107 ↗
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