131
Participants
Start Date
September 30, 2001
Primary Completion Date
November 30, 2002
Study Completion Date
November 30, 2002
insulin detemir
Subjects were dosed according to individual requirements. Injected subcutaneously (s.c. under the skin) twice daily in the morning and at bedtime for 10 weeks after an initial 6-week titration in treatment period 1 followed by 10 weeks after an initial 6-week titration in treatment period 2
insulin NPH
Subjects were dosed according to individual requirements. Injected subcutaneously (s.c. under the skin) twice daily in the morning and at bedtime for 10 weeks after an initial 6-week titration in treatment period 1 followed by 10 weeks after an initial 6-week titration in treatment period 2
insulin aspart
Subjects were dosed according to individual requirements. Injected subcutaneously (s.c. under the skin) twice daily before meals for 10 weeks after an initial 6-week titration in treatment period 1 followed by 10 weeks after an initial 6-week titration in treatment period 2
Novo Nordisk Investigational Site, Camperdown
Novo Nordisk Investigational Site, Box Hill
Novo Nordisk Investigational Site, Køge
Novo Nordisk Investigational Site, Ashford
Novo Nordisk Investigational Site, Cape Town
Novo Nordisk Investigational Site, Århus C
Novo Nordisk Investigational Site, Zagreb
Novo Nordisk Investigational Site, Città di Castello
Novo Nordisk Investigational Site, Perugia
Novo Nordisk Investigational Site, Linköping
Novo Nordisk Investigational Site, Trelleborg
Lead Sponsor
Novo Nordisk A/S
INDUSTRY