RecruitingObesity

A Research Study Comparing Different Ways of Increasing the Dose of NNC0662-0419 in Participants With Obesity

Eligible age

18+ yrs

Accepts

All genders

Locations

17 states

Healthy volunteers

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

The purpose of the study is to find out if NNC0662-0419 is safe and effective for treating participants living with obesity.

Sponsor: Novo Nordisk A/S

✓ Male or female (sex assigned at birth, inclusive of all gender identities).
✓ Age 18 years or above at the time of signing the informed consent.
✓ Body mass index (BMI) greater than or equal to (≥) 30.0 kilogram per square meter (kg/m\^2) at screening.
✓ Participant must have a desire and be committed to lose at least 25 percentage (%) of their body weight from randomisation.

✕ Known or suspected hypersensitivity to study intervention(s) or related products.
✕ Treatment with any medication prescribed for the indication of obesity or weight management (e.g. glucagon-like-peptide-1 (GLP-1) receptor agonists (RA), dual GLP-1/gastric inhibitory peptide (GIP) RAs (or any other GLP-1 based treatment) or amylin analogues)) within 90 days before screening.
✕ Glycated haemoglobin (HbA1c) ≥ 6.5% (48 Millimoles per mole \[mmol/mol\]) as measured by the central laboratory at screening.
✕ History of type 1 or type 2 diabetes mellitus.