此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

A Phase II/III Clinical Study of SIM0811 in the Treatment of Acute Ischemic Stroke

2026年11月5日 更新者:Jiangsu Simcere Pharmaceutical Co., Ltd.

A Phase II/III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Evaluate the Safety and Efficacy of SIM0811 Injection in Patients With Acute Ischemic Stroke

The study will evaluate the efficacy and safety of SIM0811 in participants with acute ischemic stroke who are present within 4.5 to 24 hours since last known well. The main questions it aims to answer are:

  1. Does SIM0811 improve overall functional outcome, measured by the ability to perform daily activities independently without help 90 days after treatment?
  2. What medical problems do participants have when taking SIM0811? Researchers will compare different doses of SIM0811 to a placebo (a look-alike substance that contains no drug) to see if SIM0811 works to treat acute ischemic stroke.

Participants will:

  1. Receive SIM0811 or a placebo .
  2. Receive standard medical care for stroke. On the first day, all participants will also take an aspirin pill or an aspirin placebo to keep the treatment assignment a secret.
  3. Stay in the hospital for a few days to undergo medical tests, including CT or MRI scans and blood draws.
  4. Return to the clinic for follow-up visits for up to 90 days to check their recovery and overall health.

研究概览

研究类型

介入性

注册 (估计的)

1092

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥ 18 years.
  2. Time from last known well: 4.5 to 24 hours.
  3. Acute ischemic stroke in a supratentorial territory, with corresponding clinical manifestations, and symptomatic high-grade stenosis or complete occlusion of the culprit vessel, involving the middle cerebral artery (MCA) M1, M2, or distal branches, the anterior cerebral artery (ACA), or the posterior cerebral artery (PCA).
  4. NIHSS score of 6-25 for the current stroke.
  5. Pre-stroke mRS ≤ 1.
  6. Female participants of childbearing potential and male participants whose partners are of childbearing potential must agree to use a highly effective contraceptive method from the time of informed consent signature until 6 months after the last dose of investigational product, and to refrain from donating sperm/ova.
  7. A written informed consent form approved by the Ethics Review Committee/Institutional Review Board (IRB), voluntarily signed by the patient or their legally authorized representative

Exclusion Criteria:

  1. Planned to undergo endovascular treatment or planned to receive thrombolytic drug therapy
  2. NIHSS consciousness score 1a > 2
  3. .Head, neck, or aortic dissection
  4. History of intracranial hemorrhage
  5. Ischemic stroke, severe traumatic brain injury, or intracranial/spinal surgery within 3 months; internal bleeding within 3 weeks; major surgical operation or trauma within 2 weeks; arterial puncture at a non-compressible site within the past week; active internal bleeding
  6. Uncontrolled hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 100 mmHg)
  7. Known bleeding tendency (hereditary or acquired) or any severe coagulation disorder. Specifically: platelet count < 100,000/μL, international normalized ratio (INR) > 1.7, aPTT > 40 seconds, or prothrombin time > 15 seconds
  8. Therapeutic-dose heparin or low molecular weight heparin within 24 hours
  9. Use of oral anticoagulants within 48 hours, including vitamin K antagonists, thrombin inhibitors, or factor Xa inhibitors, or other investigational anticoagulant drugs
  10. Use of platelet glycoprotein IIb/IIIa receptor inhibitors within 48 hours
  11. Uncorrected blood glucose level > 22.22 mmol/L or < 2.78 mmol/L during screening (participants whose blood glucose level is subsequently corrected may be considered for enrollment upon investigator assessment)
  12. Severe neurological or psychiatric disorders that affect study follow-up or neurological function assessment
  13. Clinically significant severe renal impairment, or estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m²
  14. Severe hepatic impairment, such as aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) and/or total bilirubin (TBIL) ≥ 2 × ULN, or known pre-existing congenital disorder of bilirubin metabolism
  15. Within 3 months: acute ST-elevation myocardial infarction (MI), and/or acute decompensated heart failure, and/or QTc > 520 ms, and/or hospitalization due to acute coronary syndrome, MI, or cardiac arrest, or non-elective coronary intervention; or New York Heart Association (NYHA) heart failure Class III/IV; or known ventricular tachycardia
  16. History of hemolytic anemia of any cause, currently under treatment or not meeting the criteria for cure
  17. Known allergy or intolerance to SIM0811 or its formulation excipients, or to aspirin
  18. Women who are pregnant or breastfeeding, or women with a positive pregnancy test
  19. Participation in other drug or device clinical studies within 3 months prior to screening
  20. End-stage disease with expected survival of less than 1 year
  21. Any other condition that, in the opinion of the investigator, makes the subject unsuitable for participation in this trial

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:SIM0811 2 Dose Level A (Phase II)

Participants receive SIM0811 Dose Level A.

Participants receive SIM0811 Dose Level A.

实验性的:SIM0811 Dose Level B (Phase II)

Participants receive SIM0811 Dose Level B.

Participants receive SIM0811 Dose Level B.

实验性的:SIM0811Dose Level C (Phase II)

Participants receive SIM0811 Dose Level C.

Participants receive SIM0811 Dose Level C.

安慰剂比较:Placebo(Phase II)

Participants receive SIM0811 placebo.

Participants receive SIM0811 placebo

实验性的:SIM0811(Phase III)

Participants receive the selected target dose of SIM0811.

Participants receive the selected target dose of SIM0811

安慰剂比较:Placebo (Phase III)

Participants receive SIM0811 placebo.

Participants receive SIM0811 placebo.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Proportion of patients achieving a modified Rankin Scale (mRS) score of 0-1 at Day 90
大体时间:Day 90
Day 90

次要结果测量

结果测量
大体时间
mRS distribution at Day 30 and 90;
大体时间:Day30 Day 90
Day30 Day 90
Proportions of symptomatic intracranial hemorrhage within 36 h, intracranial hemorrhage, and major extracranial hemorrhage 90-day mortality
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Any Adverse Event (AE)
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Treatment-Related Adverse Events (TRAEs)
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Serious Adverse Events (SAEs)
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Clinically Significant Abnormal Laboratory Values
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Clinically Significant Abnormal Vital Signs
大体时间:Day 0-Day 90
Day 0-Day 90
Number of Participants With Clinically Significant Abnormal Physical Examination Findings
大体时间:Day 0-Day 90
Day 0-Day 90

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:yongjun Wang, professor、Beijing Tiantan Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月30日

初级完成 (估计的)

2029年6月30日

研究完成 (估计的)

2029年6月30日

研究注册日期

首次提交

2026年10月23日

首先提交符合 QC 标准的

2026年10月23日

首次发布 (实际的)

2026年10月29日

研究记录更新

最后更新发布 (实际的)

2026年11月6日

上次提交的符合 QC 标准的更新

2026年11月5日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅