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Insulin degludec/liraglutide (IDegLira) was effective across a range of dysglycaemia and body mass index categories in the DUAL V randomized trial.

Diabetes Obes Metab · 2018

Last updated 2026-05-28

In a 26-week study of people with type 2 diabetes whose blood sugar was not well controlled on basal insulin, the combination drug IDegLira lowered blood sugar (by 1.0%–2.5%) and fasting blood glucose (by 1.5%–1.9%) across all starting levels of blood sugar, weight, and BMI. Compared with insulin glargine, IDegLira also led to weight loss instead of weight gain and caused fewer low blood sugar episodes, with more participants reaching a target blood sugar level of less than 7%.

AI summary of the abstract below.

JournalDiabetes Obes Metab, 2018
Citations14
Relative citation ratio0.58
NIH percentile33
Molecules liraglutide
Conditions studied Type 2 Diabetes, Obesity

Abstract

This study assessed the efficacy of insulin degludec/liraglutide (IDegLira) vs insulin glargine U100 (IGlar) across categories of baseline glycated haemoglobin (HbA1c; ≤7.5%, >7.5% to ≤8.5% and >8.5%), body mass index (BMI; <30, ≥30 to <35 and ≥35 kg/m ) and fasting plasma glucose (FPG; <7.2 and ≥7.2 mmol/L) in patients with type 2 diabetes (T2D) uncontrolled on basal insulin, using post hoc analyses of the DUAL V 26-week trial. With IDegLira, mean HbA1c was reduced across all baseline HbA1c (1.0%-2.5%), FPG (1.5%-1.9%) and BMI categories (1.8%-1.9%), with significantly greater reductions compared with IGlar U100. For all HbA1c, FPG and BMI categories, IDegLira resulted in weight loss and IGlar U100 in weight gain; hypoglycaemia rates were lower for IDegLira vs IGlar U100. More patients achieved HbA1c <7% with IDegLira than IGlar U100 across all HbA1c (59%-87% vs 31%-66%), FPG (71%-74% vs 40%-51%) and BMI categories (71%-73% vs 40%-54%). IDegLira improved glycaemic control and induced weight loss in patients with T2D previously uncontrolled on basal insulin, across the categories of baseline HbA1c, FPG or BMI that were tested.

Verbatim abstract via PubMed 28643425 ↗

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