A Research Study of NNC0165-1562 and Semaglutide in People Who Are Overweight or Obese

PHASE1CompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

June 18, 2018

Primary Completion Date

July 27, 2019

Study Completion Date

July 27, 2019

Conditions
Metabolism and Nutrition DisordersOverweight or Obesity
Interventions
DRUG

NNC0165-1562

Participants will receive NNC0165-1562 subcutaneous (s.c., under the skin) injection(s) once-weekly for 20 weeks. The dose will be escalated over 16 weeks to a final dose level that will be maintained for 4 weeks.

DRUG

Semaglutide

Participants will receive semaglutide s.c. injection(s) once-weekly for 20 weeks. The dose will be escalated over 16 weeks to a final dose level that will be maintained for 4 weeks.

DRUG

Placebo (NNC0165-1562)

Participants will receive placebo (NNC0165-1562) s.c. injection(s) once-weekly for 20 weeks.

Trial Locations (2)

68502

Novo Nordisk Investigational Site, Lincoln

85283

Novo Nordisk Investigational Site, Tempe

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY