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NCT07509645RecruitingPhase 3

Efficacy and Safety of Interleukin-6 Receptor Inhibitor Combined With Endovascular Treatment in Patients With Acute Posterior Circulation Large Vessel Occlusion Stroke

Efficacy and Safety of Interleukin-6 Receptor Inhibitor Combined With Endovascular Treatment in Patients With Acute Posterior Circulation Large Vessel Occlusion Stroke: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial-3

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

This is an investigator-initiated phase III clinical trial employing a randomized, double-blind, placebo-controlled design. The primary objective of this study is to investigate the efficacy and safety of an interleukin-6 inhibitor (tocilizumab) combined with endovascular therapy in patients with acute posterior circulation large-vessel occlusion stroke.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
348 (estimated)
First submitted
27 Mar 2026
Start date
22 Apr 2026
Primary completion date
20 Apr 2027
Lead sponsor
Capital Medical University
Diseases
Stroke
NCT number
NCT07509645

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 348
  • From 22 Apr 2026 to the primary completion date, 20 Apr 2027
  • 30 sites 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

  • Concurrent malignant tumors or severe systemic diseases with expected survival of less than 90 days;
  • Participation in another interventional clinical study within 30 days before randomization or currently participating in another interventional clinical study;
  • Any circumstance that, as assessed by the investigators, might result in harm to the patients if study therapy is initiated;

Other illness

  • Intracerebral hemorrhage, epidural hematoma, subdural hematoma, intraventricular hemorrhage, or subarachnoid hemorrhage;
  • Pre-stroke modified Rankin scale (mRS) score \>1;
  • Known allergy to tocilizumab or excipients;
  • Known allergy to iodinated contrast agents;
  • History of congenital or acquired bleeding disorders, coagulation factor deficiency diseases, or thrombocytopenic diseases;
  • Severe mental disorders or inability to comply with informed consent and follow-up requirements due to dementia;
  • Presence of autoimmune diseases or use of immunosuppressive drugs;
  • Systemic infectious diseases;
  • Other conditions that the investigator considers might affect compliance or preclude participation in this study.

Lab values

  • Neutrophils \< 2 × 10\^9 /L;
  • Platelets \< 100 × 10\^9 /L;
  • Blood glucose \<2.8 mmol/L (50 mg/dL) or \>22.2 mmol/L (400 mg/dL);
  • Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels \>2 times the upper limit of normal;
  • Known recent or current serum creatinine \>2 times the upper limit of normal or estimated glomerular filtration rate (eGFR) \<60 mL/min;

Other

  • Anticipated difficulty in completing endovascular treatment due to vascular tortuosity;
  • Systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg despite blood pressure control;
  • Pregnant, lactating, or planning pregnancy within 90 days;

Who the study is looking for

  • Age 18 years or older, of either sex;
  • Acute ischemic stroke caused by occlusion of the basilar artery;
  • Decide to undergo emergency endovascular treatment;
  • Time from stroke onset to groin puncture within 24 hours;
  • National Institutes of Health Stroke Scale (NIHSS) ≥ 10;
  • Posterior circulation Alberta Stroke Program Early computed tomography score (pc-ASPECTS) ≥ 6;
  • Signed informed consent from the patients or the legally authorized representatives.

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

Full criteria on ClinicalTrials.gov

Sites (30)

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

SiteCityCountrySite status
Anyang People's Hospital
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AnyangChinaRecruiting
Capital Medical Univercity Xuanwu Hospital
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BeijingChinaRecruiting
Liuyang Jili Hospital
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GuankouChinaRecruiting
Junxian People's Hospital
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HebiChinaRecruiting
Heyuan People's Hospital
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HeyuanChinaRecruiting
Suixi County Hospital
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HuaibeiChinaRecruiting
Jiaxing First People's Hospital
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JiaxingChinaRecruiting
People's Hospital of Linyi
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LinyiChinaRecruiting
Lishui Central Hospital
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LishuiChinaRecruiting
Luoyang Central Hospital
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LuoyangChinaRecruiting
Huazhou People's Hospital
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MaomingChinaRecruiting
Nanyang Central Hospital
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NanyangChinaRecruiting
Puyang Oiled General Hospital
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PuyangChinaRecruiting
Qinhuangdao Second People's Hospital
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QinhuangdaoChinaRecruiting
Shangqiu First People's Hospital
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ShangqiuChinaRecruiting
Ningling County Hospital
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ShangqiuChinaRecruiting
Suzhou Municipal Hospital
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SuzhouChinaRecruiting
Taizhou enze Hospital
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TaizhouChinaRecruiting
Yutian County Hospital
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TangshanChinaRecruiting
Tangshan Gongren Hospital
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TangshanChinaRecruiting
Wenzhou People's Hospital
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WenzhouChinaRecruiting
Xiangyang First People's Hospital
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XiangyangChinaNot yet recruiting
Xianyang First People's Hospital
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XianyangChinaRecruiting
The First Affiliated Hospital of Henan Medical University
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XinxiangChinaRecruiting
Yancheng First People's Hospital
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YanchengChinaRecruiting
People's Hospital of Yueqing
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YueqingChinaRecruiting
Yuncheng Central Hospital
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YunchengChinaRecruiting
Shenqiu County Hospital
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ZhoukouChinaRecruiting
People's Hospital of Xihua
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ZhoukouChinaRecruiting
Zibo Central hospital
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ZiboChinaRecruiting

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