A New Highly Concentrated Insulin Aspart AT278 (500 U/mL) Demonstrates Ultra-Rapid Pharmacokinetic and Pharmacodynamic Properties in Type 2 Diabetes Regardless of BMI.

Diabetes Obes MetabJul 30, 2026 (epub)
Clinical ResearchEndocrinologyOpen access

Eva Svehlikova, Christina Gatschelhofer, Bettina Lackner et al.

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In 30 seconds

This randomized controlled trial evaluated the pharmacokinetics and pharmacodynamics of a new concentrated insulin aspart formulation (AT278-U500) in 41 overweight and obese individuals with type 2 diabetes. AT278-U500 demonstrated significantly faster insulin absorption (t Early50%Cmax: 9 min) and a greater glucose-lowering effect within the first hour compared to standard insulin aspart and U500 human regular insulin.

Key findings

  • AT278-U500 had a t Early50%Cmax of 9 min, compared to 35 min for InsAsp-U100 and 55 min for HumIns-U500.
  • The glucose-lowering effect (AUC GIR,0-60min) was 2.02 times higher for AT278-U500 than InsAsp-U100.
  • No inverse relationship between BMI and AUC GIR,0-60min was observed with AT278-U500.

Why it matters

The findings suggest that AT278-U500 could provide a more effective prandial insulin option for patients with type 2 diabetes, particularly those who are insulin-resistant and require high-dose therapy, regardless of their BMI.

Source

Published in Diabetes Obes Metab. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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