LivingGLP1
Study S000785

Investigation of the Safety and Efficacy of Once Weekly NNC0519-0130 in Participants With Type 2 Diabetes - a Dose Finding Study

Registration

Registration
NCT06326047
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
299
Start
2024-03-18
Primary completion
2025-09-19
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:NNC0519-0130; DRUG:Placebo; DRUG:Trizepatide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1291-9196; REGISTRY:jRCT2031230704

Registered primary outcomes

  • Change in Glycated haemoglobin (HbA1c) [From baseline (week 0) to 12 weeks on a given maintenance dose]

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