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Glucagon-like peptide-1 receptor agonist
Semaglutide for Coronary Artery Disease (STOP Trial)
Phase 4
Waitlist Available
Led By Matthew Budoff, MD
Research Sponsored by Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
STOP Trial Summary
This trial will study whether the diabetes medication Semaglutide can help treat atherosclerosis, or hardening of the arteries.
Eligible Conditions
- Coronary Artery Disease
- Type 2 Diabetes
STOP Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Rate of change in non-calcified plaque volume
Secondary outcome measures
Rate of change in total plaque volume
STOP Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: SemaglutideActive Control1 Intervention
Semaglutide 2mg/1.5 ml (1.34 mg/ml) Prefilled pen for SQ injection
Group II: PlaceboPlacebo Group1 Intervention
Placebo 1.5 ml, pen-injector for SC injection.
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Who is running the clinical trial?
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical CenterLead Sponsor
101 Previous Clinical Trials
46,161 Total Patients Enrolled
8 Trials studying Coronary Artery Disease
7,736 Patients Enrolled for Coronary Artery Disease
Matthew Budoff, MDPrincipal InvestigatorLundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
7 Previous Clinical Trials
1,103 Total Patients Enrolled
2 Trials studying Coronary Artery Disease
164 Patients Enrolled for Coronary Artery Disease
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