64
Participants
Start Date
July 31, 2006
Primary Completion Date
November 30, 2006
Study Completion Date
November 30, 2006
liraglutide
0.6 mg daily for 7 days followed by 1.2 mg daily for 7 days followed by 1.8 mg daily for 7 days. Injected subcutaneously. Subjects are randomly allocated to two treatment sequences
placebo
Injected subcutaneously. Subjects are randomly allocated to two treatment sequences
moxifloxacin
Following the double-blinded period and a wash-out period of 7 days, subjects are re-randomised to an open-label, parallel period where a single dose of 400 mg moxifloxacin (tablets) is administered as positive control
placebo
Following the double-blinded period and a wash-out period of 7 days, subjects are re-randomised to an open-label, parallel period where single dose of oral placebo is administered
electrocardiogram (ECG)
24 hours serial ECG is collected before initial dose of 0.6 mg liraglutide, on the last dosing day of 1.2 mg liraglutide and on the last dosing day of 1.8 mg liraglutide
electrocardiogram (ECG)
Six hours after moxifloxacin or placebo single dose, 1 hour serial ECG is collected
Novo Nordisk Investigational Site, Fargo
Lead Sponsor
Novo Nordisk A/S
INDUSTRY