Related Experiment Video
Updated: May 19, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
IDegAsp: a novel soluble insulin analogs combination
Zhulin Ma1, Tina Parkner, Jens Sandahl Christiansen
1Aarhus University Hospital, Department of Endocrinology and Internal Medicine, Norrebrogade 44, Aarhus, 8000, Denmark. joli.mzl@gmail.com
IDegAsp, a novel insulin combination, offers similar glycemic control to existing options with a reduced risk of hypoglycemia. This insulin therapy shows promise for type 2 diabetes management.
Area of Science:
- Diabetes Mellitus Research
- Pharmacology
- Endocrinology
Background:
- Co-formulation of rapid- and long-acting insulins presents pharmacokinetic challenges.
- Insulin degludec aspart (IDegAsp) is a novel soluble combination of rapid-acting insulin aspart and ultra-long-acting insulin degludec.
- IDegAsp was developed to potentially improve upon existing premixed insulin suspensions.
Purpose of the Study:
- To review and summarize the pharmacological characteristics, clinical efficacy, safety, and tolerability of IDegAsp.
- To assess the potential clinical advantages of IDegAsp compared to current insulin preparations.
Main Methods:
- A comprehensive literature review was conducted.
- Published data on IDegAsp were searched through PubMed, EMBASE, and Web of Knowledge up to June 2012.
- The review focused on pharmacological profiles, clinical outcomes, and safety data.
Main Results:
- Preliminary clinical data suggest IDegAsp is safe and well-tolerated.
- IDegAsp demonstrates comparable overall glycemic control to existing insulin preparations.
- A reduced risk of hypoglycemia was observed with IDegAsp.
Conclusions:
- IDegAsp represents a promising treatment option for type 2 diabetes.
- It may be particularly beneficial for patients requiring improved control of both postprandial and fasting glucose levels.
- The combination offers a potentially safer alternative with similar efficacy to current insulin therapies.
Related Concept Videos
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Oral Hypoglycemic Agents: Glinides
Dipeptidyl Peptidase 4 Inhibitors
Insulin Formulations: Types and Delivery
Short-acting insulins are divided into rapid-acting...
Insulin: Biosynthesis, Chemistry, and Preparation
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment primarily uses...
Insulin: Dosing Regimen and Adverse Effects
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
