Start Date
July 31, 2008
Primary Completion Date
December 31, 2009
Study Completion Date
December 31, 2009
NNC 0070-0002-0349
Dose level 1: (6 subjects active, 2 subjects placebo). Subjects administered NNC 0070-0002-0349 will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
NNC 0070-0002-0349
Dose level 2: (6 subjects active, 2 subjects placebo). Subjects administered NNC 0070-0002-0349 will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
NNC 0070-0002-0349
Dose level 3: (6 subjects active, 2 subjects placebo). Subjects administered NNC 0070-0002-0349 will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
NNC 0070-0002-0349
Dose level 4 for s.c. injection (6 subjects active, 2 subjects placebo)
NNC 0070-0002-0349
Dose level 5 for s.c. injection (6 subjects active, 2 subjects placebo)
placebo
Dose level 1: NNC 0070-0002-0349 placebo. Subjects administered placebo will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
placebo
Dose level 2: NNC 0070-0002-0349 placebo. Subjects administered placebo will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
placebo
Dose level 3: NNC 0070-0002-0349 placebo. Subjects administered placebo will receive a subcutaneous injection. Subjects in the first 3 dose groups will receive two injections: one of randomized treatment (drug or placebo) and placebo
placebo
Dose level 4: NNC 0070-0002-0349 placebo for s.c. injection
placebo
Dose level 5: NNC 0070-0002-0349 placebo for s.c. injection
Lead Sponsor
Novo Nordisk A/S
INDUSTRY