This trial is conducted in Europe. The aim of this trial is to investigate steady state pharmacokinetics of biphasic insulin aspart 30 and biphasic insulin aspart 70 in subjects with type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
26
Dose individually adjusted. Administrated subcutaneously (s.c., under the skin) three times a day for 15 days in each treatment period. A wash-out period of 2-8 weeks will take place between treatment periods.
Dose individually adjusted. Administrated subcutaneously (s.c., under the skin) three times a day for 15 days in each treatment period. A wash-out period of 2-8 weeks will take place between treatment periods.
Novo Nordisk Investigational Site
Århus C, Denmark
Area under the serum insulin curve 6-14 hours after dinner at day 15
Area under the serum insulin curve 6-14 hours after dinner at day 1
Area under the serum insulin curve 0-6 hours after dinner
Area under the curve 0-24 hours
Serum insulin
Apparent t½ (apparent elimination half life)
Cmax, maximum concentration
tmax, time to reach Cmax
Adverse events
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