LivingGLP1
Study S000718

Efficacy and Safety of Co-administered Cagrilintide and Semaglutide (CagriSema) s.c. in Doses 2.4 mg/2.4 mg and 1.0 mg/1.0 mg Once Weekly Versus Placebo in Participants With Type 2 Diabetes as Add on to Once-daily Basal Insulin With or Without Metformin

Registration

Registration
NCT06323161
Acronym
REIMAGINE 3
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
274
Start
2024-03-26
Primary completion
2025-09-09
Lead sponsor
Novo Nordisk A/S
Conditions
Type 2 Diabetes
Interventions
DRUG:Cagrilintide; DRUG:Semaglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1283-0754; OTHER:2022-502679-43

Registered primary outcomes

  • Change in Glycated Haemoglobin (HbA1c) [From baseline (week 0) to end of treatment (week 40)]

Linked records (1)

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
R0004786Cagrilintide-semaglutide (CagriSema) as an add-on to basal insulin in adults with type 2 diabetes (REIMAGINE 3): a randomised, double-blind, placebo-controlled, multicentre, phase 3 study.
Rosenstock J, Lancet (London, England)
2026Randomized trialPMID 42251856DOIcites ClinicalTrials.gov:NCT06323161; registry reference DERIVED:42251856