This trial is conducted in Japan. The aim of this trial is to investigate the pharmacokinetics and pharmacodynamics of biphasic insulin aspart 30 (NN-X14Mix30) and biphasic insulin aspart 50 (NN-X14Mix5050) in subjects with type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
10
Single dose administered subcutaneously (s.c., under the skin) on two dosing vists. A wash-out period of 2-28 days will take place between dosing visits
Single dose administered subcutaneously (s.c., under the skin) on two dosing vists. A wash-out period of 2-28 days will take place between dosing visits
Novo Nordisk Investigational Site
Tokyo, Japan
The maximum insulin aspart concentration
The area under the insulin aspart curve
tmax, the time to maximum insulin aspart concentration
t½, terminal half-life
The area under the glucose infusion rate (GIR) profile
GIRmax, maximum glucose infusion rate value
tmaxGIR, time to maximum glucose infusion rate value
The area under the glucose infusion rate profile
Vital signs (blood pressure and pulse)
Adverse events
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