This trial is conducted in Europe. The aim of this trial is to investigate the bioequivalence of two formulations of biphasic insulin aspart 70 in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
A single dose administrated subcutaneously (s.c., under the skin) on two separate dosing visits. A wash-out period of 6-12 days will take place between dosing visits
Novo Nordisk Investigational Site
Neuss, Germany
Area under the insulin aspart curve in the interval from 0-16 hours
Cmax, maximum insulin aspart concentration
tmax, time to maximum insulin aspart concentration
Area under the insulin aspart curve
Mean residence time (MRT)
t½, terminal half-life
Incidence of hypoglycaemic events
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.