Insulin aspart is a recombinant analogue of human insulin. Following subcut
aneous insulin injection (0.15 to 0.2 U/kg), significantly higher serum ins
ulin concentrations an achieved in a shorter time with insulin aspart than
with human insulin. The subsequent decline in serum insulin concentrations
is also more rapid with insulin aspart.
In healthy individuals undergoing euglycaemic glucose clamp testing, glucos
e infusion rates were higher and reached maximum concentrations significant
ly earlier after insulin aspart than after human insulin.
Interindividual variability in pharmacodynamic and pharmacokinetic paramete
rs with insulin aspart was generally less than that with human insulin, whe
reas the intraindividual variability in these parameters was similar after
each insulin.
In patients with type 1 diabetes postprandial glucose excursions were less
pronounced with insulin aspart than human insulin. Daytime glucose control
was better and minimum glucose levels during the night were not as low with
insulin aspart as with human insulin.
In diabetic patients treated with insulin aspart there was generally a lowe
r frequency of hypoglycaemic events than in patients treated with human ins
ulin.