This trial was conducted in Europe. The aim of this study was to investigate the total exposure of NN5401 (insulin degludec/insulin aspart) in children, adolescents and adult subjects with type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
38
Insulin degludec/insulin aspart administered as a single subcutaneous injection (under the skin).
Novo Nordisk Investigational Site
Hanover, Germany
Area under the serum insulin degludec concentration-time curve
Time frame: from 0 to infinity after single-dose
Area under the serum insulin aspart concentration-time curve
Time frame: from 0 to 12 hours after single-dose
Maximum observed insulin degludec concentration of NN5401 (insulin degludec/insulin aspart) observed
Time frame: from 0 to 57 hours after single-dose
Maximum observed insulin aspart concentration of NN5401 (insulin degludec/insulin aspart) observed
Time frame: from 0 to 12 hours after single-dose
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