A Two Part Trial Investigating the Safety of NN9925 in Healthy Male Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

March 12, 2010

Primary Completion Date

September 16, 2010

Study Completion Date

September 16, 2010

Conditions
DiabetesDiabetes Mellitus, Type 2Healthy
Interventions
DRUG

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

DRUG

NN9925 (i.v.)

As an active comparator, one standard dose will be given i.v. (into the vein) at one study visit

DRUG

placebo

Subjects will receive a single dose of placebo as a comparator to NN9925, at all dose levels

DRUG

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

DRUG

placebo

Subjects will be randomised to receive a single dose of placebo

Trial Locations (1)

NG11 6JS

Novo Nordisk Investigational Site, Nottingham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY

NCT01087645 - A Two Part Trial Investigating the Safety of NN9925 in Healthy Male Subjects | Biotech Hunter | Biotech Hunter