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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 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

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.

Find a Location

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

Frequently Asked Questions

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~24 spots leftby Apr 2025