LivingGLP1
Study S001765

Efficacy and Safety of Once-weekly Subcutaneous UBT251 in Participants With Type 2 Diabetes - a Dose-finding Study

Registration

Registration
NCT07668388
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
RECRUITING
Enrollment
300
Start
2026-06-22
Primary completion
2027-10-04
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:UBT251; DRUG:UBT251 Placebo; DRUG:Semaglutide; DRUG:Semaglutide Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1329-7014; OTHER:2026-525465-42

Registered primary outcomes

  • UBT251: Change in glycated haemoglobin (HbA1c) [From baseline (week 0) to 12 weeks on a given maintenance dose (week 16, 28 and 40)]

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