About this trial
A prospective, multicenter, open-label, randomized controlled study to assess the effects of early intensive lipid-lowering initiated before endovascular treatment setting on (i) functional outcome in patients with acute ischemic stroke between preoperative intensive lipid-lowering therapy with PCSK9 inhibitor (PCSK9i) and guideline-recommended standard of care (SoC)(ii) safety in these patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults (age 18 years and older);
Imaging diagnosis of acute ischemic stroke with anterior circulation large vessel occlusion (including: internal carotid artery, middle cerebral artery M1 and M2, anterior cerebral artery A1 and A2);
Planned to undergo endovascular intervention within 24 hours of symptom onset (or last known well time) according to local guidelines;
Provision of informed consent by the patient or his/her legally authorized representative (or by an appropriate agent according to local requirements).
Disqualifiers
ASPECTS score ≤5 on cranial CT imaging;
Pre-existing functional impairment, with mRS score >2;
Patients who are allergic to PCSK9 inhibitors;
Patients who have received PCSK9 monoclonal antibody within 1 month prior to enrollment or PCSK9 siRNA therapy within 6 months prior to enrollment;
Trial design
Parallel
Treatments tested in this trial
guideline-recommended SoC
DrugGuideline-recommended SoC, including but not limited to oral lipid-lowering drugs, antiplatelet aggregation drugs, anticoagulant drugs, antihypertensive drugs, etc. It is to be determined by the investigator based on the subject's treatment needs.
Recaticimab (intensive)
DrugRecaticimab is added to the guideline-recommended SoC. After randomization and before endovascular interventional treatment, patients will receive a subcutaneous injection of Recaticimab. The specific method is: Recaticimab 450 mg (3 vials) as a single subcutaneous injection, until the end of the follow-up for this study.
Treatment groups
Trial outcomes
Primary outcomes
favorable functional outcome (defined as an mRS score of 0-2)
the rate (%) of good functional outcome at 90 days (modified Rankin Scale \[mRS\] score 0-2). Modified Rankin Scale scores of 0 or 1 indicate good function without or with symptoms but not disability, score of 2 indicates slight disability but independence, 3 to 5 indicate increasing levels of disability (and dependency), and a score of 6 indicates death.
Secondary outcomes
mRS ordinal score
Modified Rankin Scale scores of 0 or 1 indicate good function without or with symptoms but not disability, score of 2 indicates slight disability but independence, 3 to 5 indicate increasing levels of disability (and dependency), and a score of 6 indicates death.
Change from baseline in NIHSS score
0-42, higher scores indicates worse severity
Change from baseline in LDL-C
Change from baseline in LDL-C at 14±3 days or before discharge
Change in inflammatory markers
Change from baseline in inflammatory markers at 14±3 days or before discharge;
Sponsors and contacts
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