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Active, not recruitingNCT06081803EVO-STEMIUpdated Jun 19, 2025

Evolocumab in STEMI

A Phase 3 interventional study of Repatha® in ST Elevation Myocardial Infarction, sponsored by Sejong General Hospital. Active, not recruiting at 1 site in Korea, Republic of. Open to participants aged 30 Years to 80 Years. Per ClinicalTrials.gov, last updated 2025-06-19.

Sponsored by Sejong General Hospital · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as active, not recruiting.
  • Registered 2 years 9 months after the study started (first participant enrolled Dec 2020, registered Sep 2023).
Phase
Phase 3
Study type
Interventional
Enrollment
166
Allocation
Randomized
Ages
30 Years to 80 Years
Sex
All
01

Study summary

The goal of this clinical trial is to compare the size of myocardial infarct between evolocumab and control groups in patients with ST segment elevation myocardial infarction who undergoing primary percutaneous coronary intervention(PCI). All study participants will undergo a cardiac MRI 4 weeks after primary reperfusion. The evolocumab group will receive 420 mg before PCI via subcutaneous injection.

Read the detailed description

The gold standard for the treatment of ST-segment elevation myocardial infarction (STEMI) is to rapidly restore myocardial blood flow through primary percutaneous coronary intervention (primary PCI) as soon as possible. While primary PCI achieves successful reperfusion of the infarct-related epicardial coronary artery in over 90% of these patients, only approximately 35% achieve ideal reperfusion to the myocardium level. This condition is termed myocardial no-reflow or microvascular obstruction (MVO). The primary pathophysiology of MVO includes severe inflammatory reactions within the ischemic vessel, distal embolization of thrombi, microthrombi formation in the microvasculature, and microvascular spasm, tissue peri-infarct edema, and intramyocardial hemorrhage. Previous studies has reported that the use of atorvastatin 80mg before PCI can reduce myocardial injury occurring during PCI in patients with acute coronary syndrome (ACS), and can improve microvascular blood flow in STEMI patients undergoing primary PCI. Furthermore, it has been reported to improve microvascular functional impairment evaluated by microvascular resistance index in non-ST-segment elevation acute coronary syndrome patients and exhibit anti-inflammatory effects. However, Two randomized trials atorvastatin 80mg did not reduce infarct size, which was primary endpoint in STEMI patients.

Recently, strong LDL cholesterol-lowering agent, PCSK9 inhibitors, have been developed and used in clinical practice, and they seem to have pleiotropic effects similar to high-intensity statins, including anti-inflammatory and antithrombotic effects. In-vitro and vivo models have shown that the introduction of human PCSK9 increases platelet aggregation in normal adult plasma and that mice without PCSK9 exhibit decreased arterial thrombosis and thrombus stability when induced . Patients with higher levels of serum PCSK9 had higher platelet reactivity after antiplatelet therapy and an increased incidence of ischemic events following coronary intervention in ACS setting. This suggests that circulating PCSK9 contributes to arterial thrombus formation, and PCSK9 inhibition may improve this. Additionally, evolocumab is known to reduce Lp(a), which is well-known for its pro-atherosclerotic and pro-inflammatory effects, by approximately 30%.

Also, Pharmaceutically, evolocumab exhibits maximum inhibitory effect against PCSK9 within just 4 hours of injection, potentially beneficial for patients with acute myocardial infarction who need a rapid effect before the infarction fully develops.

In this clinical trial, we hypothesize that administering evolocumab before primary PCI in patients with acute STEMI may reduce MVO through its antiplatelet and anti-inflammatory effects and subsequently decrease the size of the myocardial infarction.

02

Conditions studied

  • ST Elevation Myocardial Infarction

Keywords

  • PCSK9
  • percutaneous coronary intervention
  • Infarct size
03

In context

ST Elevation Myocardial Infarction

850 studies on the registry are indexed under ST Elevation Myocardial Infarction; 197 are open to participants now.

This study's planned enrollment of 166 is below the median of 194 across 527 interventional studies indexed under ST Elevation Myocardial Infarction.

Browse ST Elevation Myocardial Infarction studies →

Lead sponsor

Sejong General Hospital is the lead sponsor of 8 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Typical ischemic chest pain persists for more than 30 minutes
  • An elevation of an ST segment greater than 1 mm in two consecutive leads or new-onset left bundle branch block
  • Presenting more than 12 hours after the onset of symptoms

Exclusion criteria

Exclusion Criteria:

  • Previous history of myocardial infarction
  • Previous history of coronary bypass surgery
  • Cardiogenic shock that lasts more than 10 minutes or cardiac arrest
  • Occlusion of the left main coronary artery
  • Pregnant or have a plan of pregnancy
  • Serum creatinine level is >2.5mg/dL or dialysis is required
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
166 participants (estimated)

Study arms

  • Experimental
    Evolocumab group

    Evolocumab 420mg subcutaneous injection before primary PCI

    Drug: Repatha®

  • No intervention
    Control group

    without Evolocumab 420mg before primary PCI

Interventions

  • Repatha® 140mg x 3 pens subcutaneous injection

06

What researchers measure

Primary outcomes

  1. Myocardial infarct size

    assessed by cardiac MRI

    Time frame: 1 month after primary reperfusion

Secondary outcomes

  1. The incidence of MVO

    assessed by cardiac MRI

    Time frame: 1 month after primary reperfusion

Other outcomes

  1. ST segment resolution

    assessed by 12-leads ECG

    Time frame: 1 hour after primary reperfusion

  2. Area under the curve of enzymatic infarct size

    Time frame: within 48 hours after primary reperfusion

  3. Myocardial blush grade

    assessed by coronary angiography

    Time frame: Immediate after primary reperfusion

  4. Corrected TIMI frame count

    assessed by coronary angiography

    Time frame: Immediate after primary reperfusion

  5. TIMI myocardial perfusion grade

    assessed by coronary angiography

    Time frame: Immediate after primary reperfusion

  6. The change of LDL-Cholesterol from baseline

    Time frame: 1 month after primary reperfusion

  7. The change of Lipoprotein (a) from baseline

    Time frame: 1 month after primary reperfusion

  8. Platelet reactivity on treatment

    Assessed by Verifynow

    Time frame: 1 month after primary reperfusion

  9. Hs-CRP level

    Time frame: 1 month after primary reperfusion

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Dec 2020 (actual). Primary completion is estimated for Dec 2025, 60 months after the start.

Of 38 phase 3 interventional studies under ST Elevation Myocardial Infarction, half reached primary completion within 37 months of starting (the median), counting those still running; a quarter within 23 and three quarters within 58. This study's planned 60 months is above that.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 30, 2023
First posted
Oct 13, 2023
StartActual
Dec 5, 2020
Primary completionEst.
Dec 31, 2025
CompletionEst.
Dec 31, 2025
Last update
Jun 19, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06081803
Lead sponsor
Sejong General Hospital
Collaborators
Samsung Medical Center, National Health Insurance Service Ilsan Hospital, Chonnam National University Hospital, Daegu Catholic University Medical Center, Catholic University of Korea Eunpyeong St. Mary's Hospital
Responsible party
Hyun Jong Lee (MD, PhD, Sejong General Hospital) — Principal investigator
First posted
Oct 13, 2023
Start date
Dec 5, 2020
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jun 19, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Evolocumab

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