21
Participants
Start Date
November 30, 2006
Primary Completion Date
April 30, 2007
Study Completion Date
April 30, 2007
liraglutide
Administered with daily subcutaneous injections for approximately 3 weeks in each treatment period in random order
placebo
Administered with daily subcutaneous injections for approximately 3 weeks in each treatment period in random order
levonorgestrel / ethinylestradiol
One single oral tablet after the liraglutide or placebo dose administration at the end of each treatment period
Novo Nordisk Investigational Site, Uppsala
Lead Sponsor
Novo Nordisk A/S
INDUSTRY