A First-in-human Research Study on How NNC0721-8060 Works in People Living With Overweight or Obesity
Part of paid clinical trials in Lenexa, Kansas.
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT07767175
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 55 Years
- Healthy Volunteers
- Accepted
Interventions
- NNC0721-8060 — DRUGNNC0721-8060 will be administered subcutaneously.
- Semaglutide — DRUGSemaglutide will be administered subcutaneously.
- Placebo — DRUGPlacebo will be administered subcutaneously.
Study Details
The purpose of the study is to find out if NNC0721-8060 is safe and how it works in people living with overweight or obesity.
Key Dates
- First listed
- Aug 17, 2026
- Start date
- Aug 12, 2026
- Status verified
- Aug 2026
- Primary completion
- Sep 23, 2027
- Completion
- Sep 23, 2027
Study Design
- Enrollment
- 142 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: NNC0721-8060Participants will receive subcutaneous injection of NNC0721-8060.
- Active Comparator: SemaglutideParticipants will receive subcutaneous injection of semaglutide.
- Placebo Comparator: PlaceboParticipants will receive subcutaneous injection of placebo.
Primary Outcome Measure
Part A: Number of treatment emergent adverse events (TEAE) [ Time Frame: From Day 1 to Day 36 ]
Central Contacts
- Novo Nordisk(+1) 866-867-7178
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| ICON Early Phase Services, LLC | Lenexa | Kansas | 66219 | - |
| ICON | San Antonio | Texas | 78209 | - |
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