LivingGLP1
Study S000205

Investigation of the Safety and Efficacy of Once Weekly NNC0519-0130 in Participants With Overweight or Obesity - a Dose Finding Study

Registration

Registration
NCT06326060
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
354
Start
2024-03-18
Primary completion
2025-04-10
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:NNC0519-0130; DRUG:Placebo; DRUG:Tirzepatide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1291-9210; REGISTRY:jRCT2051230198

Registered primary outcomes

  • Relative change in body weight [From baseline (week 0) to end of treatment (week 36)]

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