Safety, Tolerability and Pharmacokinetics of Liraglutide-depot in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

October 31, 2011

Primary Completion Date

March 31, 2012

Study Completion Date

March 31, 2012

Conditions
DiabetesDiabetes Mellitus, Type 2Healthy
Interventions
DRUG

liraglutide-depot

Subjects will be randomised to receive a single dose of liraglutide-depot, at increasing dose levels, injected s.c./subcutaneously (under the skin). Progression to next dose level (max. 8) will be based on safety evaluation.

DRUG

placebo

Subjects will be randomised to receive a single dose of liraglutide-depot placebo, at increasing dose levels, injected s.c./subcutaneously (under the skin).

Trial Locations (1)

47710

Novo Nordisk Investigational Site, Evansville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY

NCT01473953 - Safety, Tolerability and Pharmacokinetics of Liraglutide-depot in Healthy Subjects | Biotech Hunter | Biotech Hunter