Study of Oral HRS-5346 in Adult Patients With Elevated Lipoprotein(a) and High Risk of Cardiovascular Events
2026年8月12日 更新者:Shandong Suncadia Medicine Co., Ltd.
A Randomized, Double-Blind Phase II Study to Evaluate the Efficacy and Safety of Oral HRS-5346 in Adult Patients With Elevated Lipoprotein(a) and High Risk of Cardiovascular Events
This study is designed to evaluate the efficacy and safety of HRS-5346 Tablets in participants with high cardiovascular event risk and elevated Lp(a), and to investigate the appropriate dosage of HRS-5346 Tablets
研究概览
研究类型
介入性
注册 (估计的)
60
阶段
- 阶段2
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
- 姓名:Na Li
- 电话号码:+8615811068575
- 邮箱:na.li.nl80@hengrui.com
学习地点
-
-
Sichuan
-
Chengdu、Sichuan、中国、610041
- West China Hospital of Sichuan University
-
首席研究员:
- Yucheng Chen
-
-
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
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Understand the specific procedures of the trial, voluntarily participate in this trial, and provide written informed consent;
- Aged ≥ 18 years on the day of signing the informed consent form;
- Body mass index (BMI) ranging from 18.5 to 40 kg/m²;
- High risk of cardiovascular events at screening;
- Lp(a) ≥ 150 nmol/L as measured by the central laboratory during the screening period;
- For participants receiving pharmacotherapy per clinical practice, they must have been on a stable treatment regimen for a specified duration prior to screening or randomization and are expected to remain on that regimen through the end of the treatment period;
- Participants (including their partners) are willing to use effective contraception from the time of signing the informed consent form until 1 month after the last administration of the study drug; female participants must have a negative serum pregnancy test and must not be breastfeeding;
- Willing and able to comply with all protocol requirements, including demonstrating adherence to study procedures prior to randomization.
Exclusion Criteria:
- Any of the following occurring within 3 months prior to screening, or between screening and randomization: major cardiac or non-cardiac surgery, coronary, carotid or peripheral arterial revascularization, stroke or transient ischaemic attack, myocardial infarction or unstable angina, acute limb ischaemia; as well as arrhythmias requiring treatment but uncontrolled; or other events deemed clinically unstable by the Investigator;
- Participants with planned or anticipated cardiac, cerebrovascular, or peripheral arterial surgery, coronary revascularization, or other major surgery during the trial period after randomization;
- History of haemorrhagic stroke or other major bleeding, or occurrence of haemorrhagic stroke or other major bleeding events between screening visit and randomization visit;
- Participants with an indication for anticoagulation but not receiving anticoagulant therapy at screening;
- History of malignancy of any organ system within 5 years prior to screening, or newly diagnosed malignancy of any organ system between screening visit and randomization visit, regardless of signs of local recurrence or metastasis;
- Prior history of diseases that significantly affect lipid levels, such as nephrotic syndrome, severe liver disease, Cushing's syndrome, etc.;
- Uncontrolled type 1 or type 2 diabetes within 6 months prior to screening, or HbA1c >8.0% at screening (a repeat confirmation is allowed);
- History of acute kidney injury within 12 months prior to screening;
- Uncontrolled hyperthyroidism or hypothyroidism at screening;
- Active infection requiring systemic antiviral or antibacterial medication prior to randomization;
- New York Heart Association (NYHA) functional class III-IV heart failure at screening, or the most recently measured left ventricular ejection fraction (LVEF) <30%;
- At screening or prior to randomization, participants suffering from major diseases that are unstable and inadequately controlled, in the judgment of the Investigator;
- Chronic, continuous, or repeated use of systemic glucocorticoids within 3 months prior to screening;
- Receipt of lipoprotein apheresis within 3 months prior to screening, or planned lipoprotein apheresis during the study period;
- Prior receipt of specific antisense or gene therapy;
- Treatment with oligonucleotides or small interfering ribonucleic acid (siRNA) within 12 months prior to screening;
- Use of weight-loss medications resulting in significant weight loss, or surgery leading to substantial weight loss within 3 months prior to screening;
- Known hypersensitivity to the active ingredient or any excipient of HRS-5346;
- Uncontrolled hypertension prior to randomization;
- eGFR < 30 mL/min/1.73 m² at screening or prior to randomization, or participants receiving dialysis;
- Alanine aminotransferase (ALT), aspartate aminotransferase (AST), or gamma-glutamyl transferase (GGT) > 2 times the upper limit of normal (ULN), or total bilirubin >1.5 times ULN at screening or prior to randomization;
- Human immunodeficiency virus infection (HIV-Ab positive), hepatitis C virus infection (HCV-RNA positive), Treponema pallidum infection (Treponema pallidum antibody positive), hepatitis B virus infection (HBsAg positive) at screening or prior to randomization;
- Creatine kinase (CK) > 3 times the upper limit of normal (ULN) prior to randomization;
- Thyroid-stimulating hormone (TSH) below the lower limit of normal (LLN) or above the upper limit of normal (ULN) during screening;
- Significant abnormal laboratory parameters at screening or prior to randomization that render the participant unsuitable for this study, as judged by the Investigator;
- History of drug or alcohol abuse or dependence in the recent past (within 1 year);
- Pregnant or breastfeeding women;
- Participation in any clinical trial of investigational drug or medical device within 3 months prior to screening, or still within 5 half-lives of the investigational product at screening, whichever is longer;
- The Investigator judges that the participant has poor adherence or any other factor rendering participation inappropriate, including but not limited to circumstances where trial participation would expose the participant to unacceptable risk or may confound study results.
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:Treatment group A: HRS-5346 Dose1
|
HRS-5346; Dose1
HRS-5346; Dose2
|
|
实验性的:Treatment group B: HRS-5346 Dose2
|
HRS-5346; Dose1
HRS-5346; Dose2
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Percentage Change in Lp(a) Levels from Baseline to Week 12
大体时间:Week 12
|
Week 12
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Percentage change in Lp(a) levels from baseline to Week 4;
大体时间:Week 4
|
Week 4
|
|
Absolute change in Lp(a) levels from baseline to Week 4 and Week 12;
大体时间:Week4, Week 12
|
Week4, Week 12
|
|
Proportion of participants with greater than 70% reduction in Lp(a) levels from baseline at Week 4 and Week 12;
大体时间:Week4, Week 12
|
Week4, Week 12
|
|
Proportion of participants achieving Lp(a) < 125 nmol/L (i.e., 50 mg/dL) at Week 4 and Week 12;
大体时间:Week4, Week 12
|
Week4, Week 12
|
|
Proportion of participants achieving Lp(a) < 75 nmol/L (i.e., 30 mg/dL) at Week 4 and Week 12;
大体时间:Week4, Week 12
|
Week4, Week 12
|
|
Incidence and severity of any adverse event (AE);
大体时间:Week0- Week 13
|
Week0- Week 13
|
|
Incidence of adverse event of special interest (AESI)
大体时间:Week0- Week 13
|
Week0- Week 13
|
|
Incidence of serious adverse event (SAE)
大体时间:Week0- Week 13
|
Week0- Week 13
|
|
Pharmacokinetic assessment: plasma concentrations of HRS-5346.
大体时间:Week0- Week 13
|
Week0- Week 13
|
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。
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9月1日
初级完成 (估计的)
2027年2月1日
研究完成 (估计的)
2027年5月1日
研究注册日期
首次提交
2026年8月12日
首先提交符合 QC 标准的
2026年8月12日
首次发布 (实际的)
2026年8月17日
研究记录更新
最后更新发布 (实际的)
2026年8月17日
上次提交的符合 QC 标准的更新
2026年8月12日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他研究编号
- HRS-5346-202
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
未定
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.