LivingGLP1
Study S003224

Safety and Efficacy of Once-weekly Subcutaneous and Once-daily Oral NNC0487-0111 in Participants With Type 2 Diabetes - a Dose Finding Study

Registration

Registration
NCT06542874
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
448
Start
2024-08-07
Primary completion
2025-10-01
Lead sponsor
Novo Nordisk A/S
Conditions
Type 2 Diabetes (T2D)
Interventions
DRUG:NNC0487-0111 subcutanous; DRUG:Placebo (NNC0487-0111 subcutanous); DRUG:NNC0487-0111 oral; DRUG:Placebo (NNC0487-0111 oral)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1296-9708; OTHER:2023-509412-28; NIH:2023

Registered primary outcomes

  • Change in HbA1c [From baseline (week 0) to end of treatment (week 36)]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0020979Efficacy and safety of once-weekly subcutaneous zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.
Mora P, Lancet (London, England)
2026Randomized trialPMID 42532080DOIcites ClinicalTrials.gov:NCT06542874; registry reference DERIVED:42532080
R0021369Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.
Mora P, Lancet (London, England)
2026Randomized trialPMID 42532079DOIcites ClinicalTrials.gov:NCT06542874; registry reference DERIVED:42532079