70
Participants
Start Date
March 12, 2010
Primary Completion Date
September 16, 2010
Study Completion Date
September 16, 2010
NN9925 (oral)
Subjects will be randomised to receive a single dose of NN9925, at escalating dose levels. Progression to next dose will be based on safety evaluation
NN9925 (i.v.)
As an active comparator, one standard dose will be given i.v. (into the vein) at one study visit
placebo
Subjects will receive a single dose of placebo as a comparator to NN9925, at all dose levels
NN9925 (oral)
Subjects will be randomised to receive a single dose of NN9925 in up to three different concentrations. The dose will be selected based on the results of part 1
placebo
Subjects will be randomised to receive a single dose of placebo
Novo Nordisk Investigational Site, Nottingham
Lead Sponsor
Novo Nordisk A/S
INDUSTRY