A Two Part Trial Investigating an Anti-obesity Drug in Overweight/Obese Male and Female Healthy Volunteers

PHASE1TerminatedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

January 5, 2010

Primary Completion Date

December 13, 2010

Study Completion Date

September 20, 2011

Conditions
Metabolism and Nutrition DisorderObesity
Interventions
DRUG

NNC 0070-0002-0453

Administration of a single subcutaneous (under the skin) dose. Up to 7 escalating dose levels will be investigated. Progression to next dose level will be based on a safety evaluation.

DRUG

'2-0453

Administration of multiple subcutaneous (under the skin) doses for 10 weeks. Up to 4 escalating dose levels will be investigated. Progression to next dose level will be based on a safety evaluation.

DRUG

placebo

Placebo will be administered as a comparator at each dose level.

Trial Locations (1)

47710

Novo Nordisk Investigational Site, Evansville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY