Effect of Liraglutide on Heart Frequency in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

July 31, 2006

Primary Completion Date

November 30, 2006

Study Completion Date

November 30, 2006

Conditions
DiabetesDiabetes Mellitus, Type 2
Interventions
DRUG

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

DRUG

placebo

Injected subcutaneously. Subjects are randomly allocated to two treatment sequences

DRUG

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

DRUG

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

PROCEDURE

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

PROCEDURE

electrocardiogram (ECG)

Six hours after moxifloxacin or placebo single dose, 1 hour serial ECG is collected

Trial Locations (1)

58104

Novo Nordisk Investigational Site, Fargo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY

NCT01516255 - Effect of Liraglutide on Heart Frequency in Healthy Volunteers | Biotech Hunter | Biotech Hunter