Skip to content
KStart free
AI InfrastructureDefenseQuantumAll studies →

A Two-armed Real-world Study of Ozempic (OW Semaglutide) to Evaluate Its Adherence and Persistence Compared With Other Anti-diabetic Drugs Among Adult T2DM Patients in China

← catalyst calendar

NCT07456774 · readout in 12 d

Sponsored by Novo Nordisk A/S (industry) · NVO — their whole pipeline →.

Phase
Status
Enrolling by invitation
Study type
Observational
Enrollment
100,000estimated
Sites
1
Country
China

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-02-13actualWhen the study began enrolling
Primary completion2026-08-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-08-31estimatedThe whole study's end, after follow-up
First posted2026-03-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Type 2 Diabetes

Primary outcomes

what the primary-completion date above is the date OF
Time to 3P major adverse cardiovascular events
measured From index date to the first composite 3P MACE (stroke, myocardial infarction, all-cause death) event or censoring event (up to 36 months)
Time to 5P MACE
measured From index date to the first composite 5P MACE (stroke, myocardial infarction, all-cause death, heart failure hospitalization, coronary revascularization) event or censoring event (up to 36 months)
Time to stroke
measured From index date to the first stroke event or censoring event (up to 36 months)
Time to myocardial infarction (MI)
measured From index date to the first MI event or censoring event (up to 36 months)
Time to heart failure (HF)
measured From index date to the first HF event or censoring event (up to 36 months)
Time to composite renal event
measured From index date to first composite renal (kidney failure: dialysis/transplantation/eGFR <15, ≥50% eGFR reduction from baseline, or kidney-related/cardiovascular death) or censoring event (up to 36 months)
Time to renal disease-related hospitalization
measured From index date to the first renal disease-related hospitalization or censoring event (up to 36 months)
Incidence rate of 3P MACE
measured From index date to the first composite 3P MACE (stroke, myocardial infarction, all-cause death) event or censoring event (up to 36 months)
Incidence rate of 5P MACE
measured From index date to the first composite 5P MACE (stroke, myocardial infarction, all-cause death, heart failure hospitalization, coronary revascularization) event or censoring event (up to 36 months)
Incidence rate of stroke
measured From index date to the first stroke event or censoring event (up to 36 months)
Incidence rate of myocardial infarction
measured From index date to the first MI event or censoring event (up to 36 months)
Incidence rate of heart failure
measured From index date to the first HF event or censoring event (up to 36 months)
Incidence rate of composite renal event
measured From index date to first composite renal (kidney failure: dialysis/transplantation/eGFR <15, ≥50% eGFR reduction from baseline, or kidney-related/cardiovascular death) or censoring event (up to 36 months)
Incidence rate of renal disease-related hospitalization
measured From index date to the first renal disease-related hospitalization or censoring event (up to 36 months)

Permalink · NVO's whole pipeline · Catalyst calendar · Every registered study · What changed