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 I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ZKLJ02 Injection in Healthy Chinese Research Participants (ZKLJ02-I)

A Randomized, Double-blind, Placebo-controlled, Dose-escalation Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Intravenous Administration of ZKLJ02 Injection in Healthy Chinese Research Participants

A randomized, double-blind, placebo-controlled, dose-escalation Phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous administration of ZKLJ02 injection in healthy Chinese research participants

研究概览

研究类型

介入性

注册 (实际的)

50

阶段

  • 阶段1

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。

学习地点

    • Yunnan
      • Kunming、Yunnan、中国
        • Yunnan Zhongke Longjin Biotechnology Co.,Ltd.

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

接受健康志愿者

是的

描述

Inclusion Criteria:

  1. Able to provide informed consent and willing to comply with the study procedures;
  2. Age between 18 and 45 years (inclusive), regardless of gender;
  3. No clinically significant past or current medical history of cardiovascular, hepatic, renal, gastrointestinal, neurological, respiratory, psychiatric, or metabolic disorders, as determined by the investigator;
  4. Physical examination, laboratory tests, 12-lead ECG, and vital signs are all normal or show abnormalities that are not clinically significant;
  5. Body mass index (BMI) between 19.0 and 26.0 kg/m^2 (inclusive); body weight not less than 50 kg for males and not less than 45 kg for females;
  6. Men with reproductive potential and women of childbearing potential must have no plans for pregnancy, sperm donation, or oocyte donation from the time of informed consent until 30 days after the final study visit, and must agree to use effective contraception.

Exclusion Criteria:

  1. Individuals with a history of definite drug or food allergy, or known allergic reaction to any component of this product;
  2. Known or suspected malignant tumors;
  3. History of unexplained syncope, symptomatic hypotension, or hypoglycemia;
  4. History or family history of long QT interval syndrome, or ECG showing QTcF >= 450 ms in males or >= 470 ms in females;
  5. History of chronic diarrhea, malabsorption, unexplained weight loss, or food intolerance;
  6. Individuals with a history of intracranial hemorrhage (e.g., after traffic accidents), stroke, or cerebrovascular disease;
  7. Any disease (e.g., acute gastritis, gastrointestinal ulcers, gastrointestinal bleeding, Henoch-Schönlein purpura, systemic lupus erythematosus, etc.) or medical history (e.g., coagulation disorders, history of intracranial hemorrhage, history of intraocular hemorrhage, history of hemophilia, history of von Willebrand disease, etc.) that, in the investigator's judgment, could alter or increase the tendency to bleed;
  8. Regular and continuous use within 3 months prior to screening of medications affecting coagulation function (e.g., clopidogrel, ticlopidine, dipyridamole, warfarin-like anticoagulants, novel oral anticoagulants such as rivaroxaban, apixaban, etc.), or prior treatment with anticoagulants such as heparin, low-molecular-weight heparin, or fibrinolytic agents;
  9. Presence of significant factors affecting normal venipuncture, such as history of heparin allergy, history of heparin-induced thrombocytopenia, inability to tolerate venipuncture, or history of needle or blood phobia;
  10. Positive test results for human immunodeficiency virus (HIV) antibody, hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, or syphilis antibody;
  11. Blood donation or blood loss of more than 500 mL within 3 months prior to screening;
  12. Participation in any other drug or medical device clinical trial within 3 months prior to screening, or currently participating in another clinical trial, or still within five half-lives of an investigational medicinal product at the time of screening;
  13. Use of any prescription medication, over-the-counter drug, or dietary supplement within 14 days or five half-lives (whichever is longer) prior to the first administration of the study drug;
  14. Hospitalization or major surgery within 6 months prior to screening;
  15. History of drug abuse within 9 months prior to screening;
  16. Individuals with a history of alcoholism or regular alcohol consumption within 9 months prior to screening, defined as more than 14 alcohol units per week (14 units = 8 bottles of beer (500 mL each, 3.5% alcohol content) or 500 g of baijiu (45% alcohol content) or 1.5 bottles of wine (750 mL each, 13% alcohol content)), or those unwilling to abstain from alcohol during the study period;
  17. Study participants who smoked more than 5 cigarettes per day in the past 6 months, or used tobacco-containing alternative products in equivalent amounts, or who cannot ensure complete abstinence from smoking during the study period;
  18. Pregnant or lactating women, those with a positive pregnancy test result, and female study participants who engaged in unprotected sexual activity within 2 weeks prior to the start of screening;
  19. Onset of acute illness during the screening phase or prior to the first administration of study medication;
  20. Consumption within 48 hours before dosing of any food or beverage containing caffeine, alcohol, xanthine, or grapefruit components (e.g., coffee, strong tea, chocolate, etc.);
  21. Positive breath alcohol test result or positive drug abuse screening result;
  22. Any individual with special dietary requirements who cannot comply with the standardized diet (e.g., intolerance to standard meals, lactose intolerance, etc.);
  23. Other conditions deemed by the investigator as unsuitable for participation in this study.

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:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:剂量组 1
Dissolve 10 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
实验性的:剂量组 2
Dissolve 20 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
实验性的:剂量组 3
Dissolve 40 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
实验性的:剂量组 4
Dissolve 80 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
实验性的:剂量组 5
Dissolve 120 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Adverse Event
大体时间:Within 24 hours of administering the experimental drug
The incidence rate of adverse events, severity and nature of adverse events, correlation between adverse events and investigational products
Within 24 hours of administering the experimental drug

次要结果测量

结果测量
大体时间
Maximum Observed Plasma Concentration (Cmax)
大体时间:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Area Under the Plasma Concentration Time Curve (AUC)
大体时间:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Time to the Maximum Plasma Concentration (Tmax)
大体时间:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Activated Partial Thromboplastin Time (APTT)
大体时间:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Prothrombin Time (PT)
大体时间:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Thrombin Time (TT)
大体时间:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Incidence rate of antidrug antibody (ADA)
大体时间:Within 7 days of administering the experimental drug
Within 7 days of administering the experimental drug

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 (实际的)

2025年8月11日

初级完成 (实际的)

2025年11月18日

研究完成 (实际的)

2025年11月18日

研究注册日期

首次提交

2026年5月18日

首先提交符合 QC 标准的

2026年6月5日

首次发布 (实际的)

2026年6月10日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月5日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • YunnanZhongkeLongjinBio
  • ChiCTR2500111786 (其他标识符:Chinese Clinical Trial Registry (ChiCTR))

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