155
Participants
Start Date
December 17, 2009
Primary Completion Date
May 7, 2010
Study Completion Date
May 7, 2010
NN9924 (oral)
Subjects will be randomized to receive a single dose of NN9924, at escalating dose levels. Progression to next dose will be based on safety evaluation.
placebo
Subjects will receive a single dose of placebo as a comparator to NN9924, at all dose levels.
NN9924 (oral)
Subjects will be randomized to receive a single dose of NN9924 in one of three different concentrations. The dose will be selected based on the results of part 1.
placebo
Subjects will be randomized to receive a single dose of placebo.
NN9924 (s.c.)
As an active comparator, one standard dose will be given s.c. (under the skin) at one study visit
NN9924 (i.v.)
As an active comparator, one standard dose will be given i.v. (into the vein) at one study visit.
Novo Nordisk Investigational Site, Harrow
Lead Sponsor
Novo Nordisk A/S
INDUSTRY