33
Participants
Start Date
September 30, 2009
Primary Completion Date
December 31, 2009
Study Completion Date
December 31, 2009
insulin degludec/insulin aspart
Single dose of 0.4 U/kg body weight injected subcutaneously (under the skin)
insulin degludec/insulin aspart
Single dose of 0.6 U/kg body weight injected subcutaneously (under the skin)
insulin degludec/insulin aspart
Single dose of 0.8 U/kg body weight injected subcutaneously (under the skin)
biphasic insulin aspart 30
Single dose of 0.4 U/kg body weight injected subcutaneously (under the skin)
biphasic insulin aspart 30
Single dose of 0.6 U/kg body weight injected subcutaneously (under the skin)
biphasic insulin aspart 30
Single dose of 0.8 U/kg body weight injected subcutaneously (under the skin)
Novo Nordisk Investigational Site, Neuss
Lead Sponsor
Novo Nordisk A/S
INDUSTRY