A Phase II/III Clinical Study of SIM0811 in the Treatment of Acute Ischemic Stroke
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:
- Does SIM0811 improve overall functional outcome, measured by the ability to perform daily activities independently without help 90 days after treatment?
- 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:
- Receive SIM0811 or a placebo .
- 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.
- Stay in the hospital for a few days to undergo medical tests, including CT or MRI scans and blood draws.
- Return to the clinic for follow-up visits for up to 90 days to check their recovery and overall health.
研究概览
地位
条件
研究类型
注册 (估计的)
阶段
- 阶段2
- 第三阶段
联系人和位置
学习联系方式
- 姓名:zhibiao song
- 电话号码:86-13641133681
- 邮箱:songzhibiao@simcere.com
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Age ≥ 18 years.
- Time from last known well: 4.5 to 24 hours.
- 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).
- NIHSS score of 6-25 for the current stroke.
- Pre-stroke mRS ≤ 1.
- 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.
- 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:
- Planned to undergo endovascular treatment or planned to receive thrombolytic drug therapy
- NIHSS consciousness score 1a > 2
- .Head, neck, or aortic dissection
- History of intracranial hemorrhage
- 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
- Uncontrolled hypertension (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 100 mmHg)
- 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
- Therapeutic-dose heparin or low molecular weight heparin within 24 hours
- Use of oral anticoagulants within 48 hours, including vitamin K antagonists, thrombin inhibitors, or factor Xa inhibitors, or other investigational anticoagulant drugs
- Use of platelet glycoprotein IIb/IIIa receptor inhibitors within 48 hours
- 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)
- Severe neurological or psychiatric disorders that affect study follow-up or neurological function assessment
- Clinically significant severe renal impairment, or estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m²
- 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
- 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
- History of hemolytic anemia of any cause, currently under treatment or not meeting the criteria for cure
- Known allergy or intolerance to SIM0811 or its formulation excipients, or to aspirin
- Women who are pregnant or breastfeeding, or women with a positive pregnancy test
- Participation in other drug or device clinical studies within 3 months prior to screening
- End-stage disease with expected survival of less than 1 year
- Any other condition that, in the opinion of the investigator, makes the subject unsuitable for participation in this trial
学习计划
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
调查人员
- 首席研究员:yongjun Wang, professor、Beijing Tiantan Hospital
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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