LivingGLP1
Study S001673

Comparative Effectiveness of Semaglutide and Dulaglutide in Patients at Low, Moderate, and High Cardiovascular Risk With Type 2 Diabetes and Overweight

Registration

Registration
NCT07619495
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
120000
Start
2026-01-20
Primary completion
2026-06-01
Lead sponsor
Brigham and Women's Hospital
Conditions
Type 2 Diabetes Mellitus; Obesity; Overweight
Interventions
DRUG:Semaglutide; DRUG:Dulaglutide
Results posted
FALSE

Registered primary outcomes

  • Composite of all-cause mortality, myocardial infarction, or stroke. [1 day after cohort entry until outcome, disenrollment, end of study period, death, 365 days after cohort entry, discontinuation (45 days grace and risk window), switch between study arms, nursing home admission, or start of any other GLP-1-RA]

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