A Trial Investigating the Pharmacokinetic and Pharmacodynamic Properties of Faster-acting Insulin Aspart in Subjects with Type 2 Diabetes Mellitus
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
61
A single dose administered subcutaneously (s.c., under the skin). The dose level will be 0.3 U/kg body weight.
A single dose administered subcutaneously (s.c., under the skin). The dose level will be 0.3 U/kg body weight.
Novo Nordisk Investigational Site
Graz, Austria
Area under the serum insulin aspart concentration-time curve
Time frame: From 0 to 30 minutes
Maximum observed serum insulin aspart concentration
Time frame: Within 0 to 12 hours after dosing
Area under the glucose infusion rate curve
Time frame: From 0 to t, where t is the last time where glucose infusion rate (GIR) exceeds zero (within 0 to 12 hours after dosing)
Maximum glucose infusion rate
Time frame: Within 0 to 12 hours after dosing
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.