LivingGLP1
Study S001875

Evaluation of Different Dose Escalation Regimens for NNC0662-0419 in Participants With Obesity

Registration

Registration
NCT07639021
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
233
Start
2026-06-09
Primary completion
2027-06-14
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:NNC0662-0419; DRUG:Semaglutide; DRUG:NNC0662-0419 Placebo; DRUG:Semaglutide placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1333-3475

Registered primary outcomes

  • Number of gastrointestinal adverse events [From week 0 to week 39]

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