IDegLira fixed-ratio combination in the real world: a retrospective observational single-center Italian experience.
Eur Rev Med Pharmacol Sci · 2020
Last updated 2026-05-28In a real-world study of Italian patients with type 2 diabetes, switching to IDegLira—a combination of insulin degludec and liraglutide—improved blood sugar control, including HbA1c and fasting glucose levels. The benefits were especially noticeable in patients previously using basal insulin or GLP-1 drugs, with effects seen as early as one month. The treatment also reduced the need for basal insulin in some patients and was effective at moderate doses.
AI summary of the abstract below.
| Journal | Eur Rev Med Pharmacol Sci, 2020 |
|---|---|
| Citations | 12 |
| Relative citation ratio | 0.74 |
| NIH percentile | 40 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
OBJECTIVE: An improvement of type 2 diabetes treatment is represented by the recent availability of a fixed-ratio combination of slow insulin degludec and GLP-1 RA liraglutide (IDegLira), which shows encouraging clinical trial results. This work represents a real-world evidence study to evaluate if the obtained clinical results are also confirmed in the clinical practice, in an Italian type 2 diabetes patients' population.
PATIENTS AND METHODS: This retrospective observational study was conducted in the Diabetology Service of the Umbria local sanitary agency (USL Umbria 1) in Perugia. The study investigated all diabetic patients >18 years, who underwent anti-diabetic treatment with basal insulin with or without the concomitant consumption of one or more oral anti-diabetic agent (BOT group) or GLP-1 RA or rapid-acting insulin bolus (BB group), with unsatisfactory glycemic control for either hypoglycemic episodes or weight gain. The observation period was February 2018 to April 2019.
RESULTS: IDegLira results to be effective in reducing HbA1c and fasting plasma glucose, especially among GLP-1 RA and BOT subgroup. In BOT group, a statistical difference was noted from the first month of treatment, also for post-prandial glycemia. Obtained results were achieved at a moderate dose of IDegLira reported during the study, which also represents a significant reduction of the amount of basal insulin in BB patients.
CONCLUSIONS: Obtained results suggest that in a real-world setting, the switch to IDegLira treatment is a valid option for patients with unsatisfactory glycemic control, or who experienced side effects such as weight gain and hypoglycemia of other insulin therapies.
Verbatim abstract via PubMed 33155225 ↗