A Research Study Looking Into How Cagrilintide Influences Food Intake and Appetite in People With Overweight or Obesity
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT07557953
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 64 Years
- Healthy Volunteers
- Not accepted
Interventions
- Cagrilintide — DRUGCagrilintide is administered subcutaneously .
- Placebo Cagrilintide — DRUGPlacebo Cagrilintide is administered subcutaneously.
Study Details
The study is testing cagrilintide, a study medicine, to understand how it affects food intake and appetite in people with overweight or obesity. Participants will receive either cagrilintide or placebo, and which treatment participants get is decided by chance. Cagrilintide is the treatment being tested, while placebo looks like the study medicine but does not contain any active medicine. The study will last for about 30 weeks.
Key Dates
- Start date
- Apr 30, 2026
- Status verified
- May 2026
- Primary completion
- Apr 13, 2027
- Completion
- Apr 13, 2027
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: CagrilintideParticipant will receive Cagrilintide subcutaneously once weekly for up to 17 weeks.
- Placebo Comparator: Placebo CagrilintideParticipant will receive placebo matched to Cagrilintide subcutaneously once weekly for up to 17 weeks.
Primary Outcome Measure
Relative change in total energy intake across ad libitum breakfast, lunch, evening meal and snack box [ Time Frame: From baseline (Day 2) to end of treatment (Day 127) ]
Central Contacts
- Novo Nordisk(+1) 866-867-7178
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