This trial is conducted in the United States of America (USA). The aim of this trial is to evaluate the the dose-response of insulin detemir and insulin NPH in subjects with type 2 diabetes of various race and ethnicity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
50
Each subject will be randomly allocated to three doses: 0.3, 0.6, and 1.2 U/kg. Administrated subcutaneously (s.c., under the skin)
Each subject will be randomly allocated to three doses: 0.3, 0.6, and 1.2 U/kg. Administrated subcutaneously (s.c., under the skin)
Novo Nordisk Investigational Site
Chula Vista, California, United States
Area under the glucose infusion rate curve
Maximum glucose infusion rate
Time to maximum glucose infusion rate.
Area under the serum insulin curve
Maximum serum insulin concentration
Time to maximum insulin concentration
Terminal rate constant of insulin
Terminal half-life of insulin
Adverse events
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