This trial is conducted in Europe. The aim of the trial is to investigate the pharmacokinetic (the exposure of the trial drug in the body) properties of FIAsp (faster-acting insulin aspart) in children, adolescents and adults with type 1 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
41
A single dose will be administered subcutaneously (s.c. under the skin)
A single dose will be administered subcutaneously (s.c. under the skin)
Novo Nordisk Investigational Site
Hanover, Germany
Area under the serum insulin aspart concentration-time curve
Time frame: From 0 to 12 hours
Maximum observed serum insulin aspart concentration
Time frame: From 0-12 hours
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