Comparative Study of Tirzepatide Versus Dulaglutide (SURPASS CVOT) or Semaglutide on Major Cardiovascular Events in Participants With Type 2 Diabetes
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Brigham and Women's Hospital
- Study ID
- NCT06779929
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tirzepatide — DRUGTirzepatide
- Dulaglutide — DRUGDulaglutide
- Semaglutide — DRUGSemaglutide
Study Details
This cohort study was initiated to emulate the design of the SURPASS-CVOT trial using observational analogues of the trial design components in a study based on insurance claims data.
Key Dates
- Start date
- Nov 1, 2024
- Status verified
- Dec 2025
- Primary completion
- Dec 1, 2025
- Completion
- Mar 1, 2026
Study Design
- Enrollment
- 70,000 participants (actual)
Arms
- Arm: TirzepatidePatients who initiated tirzepatide with no use in the prior 180 days
- Arm: DulaglutidePatients who initiate dulaglutide with no use in the prior 180 days
- Arm: SemaglutidePatients who initiate semaglutide with no use in the prior 180 days
Primary Outcome Measure
Composite CV outcome [ Time Frame: From treatment initiation to end of follow up, up to 48 months. ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Brigham and Women's Hospital | Boston | Massachusetts | 02120 | - |
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