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NCT07540741Recruiting

Efficacy and Safety of PCSK9 Inhibitors in Patients With Large-Artery Atherosclerosis (LAA) Ischemic Stroke

Efficacy and Safety of PCSK9 Inhibitors in Patients With Large-Artery Atherosclerosis (LAA) Ischemic Stroke: A Prospective Multicenter Cohort Study

Source: ClinicalTrials.gov · Last updated 23 Apr 2026

Brief summary (registry, in English)

This prospective multicenter cohort study aims to evaluate the effectiveness and safety of early PCSK9 inhibitor therapy in patients with large-artery atherosclerotic ischemic stroke. The study will compare early neurological improvement, lipid-lowering effect, 90-day functional outcome, recurrent cardio-cerebrovascular events, and safety outcomes between patients treated with evolocumab plus statin and those treated with statin alone.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
13 Apr 2026
Start date
3 Dec 2025
Primary completion date
1 Dec 2027
Lead sponsor
First Affiliated Hospital of Harbin Medical University
Diseases
Stroke
NCT number
NCT07540741

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 3 Dec 2025 to the primary completion date, 1 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior intracranial or extracranial endovascular therapy before enrollment, planned acute endovascular therapy within 90 days, or planned surgery that may affect outcome assessment.
  • Participation in another interventional clinical study within 30 days before enrollment, or concurrent participation in another interventional study that may affect outcome assessment.

Other illness

  • Hemorrhagic transformation or other intracranial hemorrhage (including hemorrhagic infarction, subarachnoid hemorrhage, subdural hematoma, or epidural hematoma), except cerebral microbleeds detected only by SWI.
  • Severe cardiac insufficiency:NYHA class III or IV.
  • Pre-existing neurologic or psychiatric disease likely to affect neurologic or functional outcome assessment; severe neurologic deficit causing loss of independent living; dementia or psychiatric disease preventing completion of follow-up.
  • Autoimmune disease (for example systemic sclerosis, systemic lupus erythematosus, Sjogren syndrome, Behcet disease, mixed connective tissue disease, or IgG4-related disease).
  • Active seizures, hypotension, hyperthyroidism, asthma, and other allergic respiratory diseases, as well as individuals with a tendency toward allergies.
  • Any other condition judged by the investigator to make participation inappropriate or to pose substantial risk.

Lab values

  • Severe hepatic dysfunction (ALT or AST \>3 x upper limit of normal) or severe renal dysfunction (serum creatinine \>2 mg/dL, eGFR \<30 mL/min/1.73 m2, or requiring dialysis).
  • Platelet count \<100 x 10\^9/L.
  • Active gastrointestinal ulcer, active bleeding tendency: corrected international normalized ratio (INR) \> 1.5, bleeding time exceeding the upper limit by more than 1 minute, or increased bleeding risk due to heparin-induced thrombocytopenia; major systemic bleeding occurring within 30 days prior to enrollment.

Other

  • Pregnancy or breastfeeding.
  • Giant intracranial tumor, giant cerebral aneurysm, or arteriovenous malformation.

Who the study is looking for

  • Age 18-80 years.
  • Acute ischemic stroke diagnosed according to the Chinese Guidelines for Diagnosis and Treatment of Acute Ischemic Stroke (2023), based on clinical and imaging criteria.
  • Large-artery atherosclerotic subtype (TOAST classification) confirmed within 72 hours after stroke onset.
  • NIHSS score 4-20 before treatment.
  • Pre-stroke modified Rankin Scale (mRS) score ≤1.
  • LDL-C ≥1.8 mmol/L before enrollment.
  • Able to use evolocumab and statin medications in accordance with the physician's instructions and the prescribing information.
  • No prior use of a PCSK9 inhibitor before enrollment.
  • Written informed consent provided by the participant or legally authorized representative.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Harbin, Heilongjiang, China, 150001
Coordinator of this site? Confirm its status
HeilongjiangChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.