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Comparative Clinical Trial of Pharmacokinetics and Pharmacodynamics of Human Insulin Injection

2026年5月27日 更新者:Zhuhai United Laboratories Co., Ltd.

A Single-Center, Randomized, Double-Blind, Two-Formulation, Single-Dose, Two-Period Crossover Clinical Trial Comparing Pharmacokinetics and Pharmacodynamics of Human Insulin Injection

A study of Clinical Trial Comparing Pharmacokinetics and Pharmacodynamics of Human Insulin Injection,in Wuhan Pulmonary Hospital (Wuhan Tuberculosis Prevention and Control Institute).To compare the pharmacokinetic and pharmacodynamics properties of a single subcutaneous dose of the human insulin injection (USLIN®R, Zhuhai United Laboratories (Zhongshan) Co., Ltd.) with the reference product (Novolin®R, Novo Nordisk Inc.) in healthy male subjects,and to evaluate the safety, tolerability, and immunogenicity of the test formulation versus the reference formulation in healthy male subjects.This single-center, randomized, double-blind, two-formulation, single-dose, two-period crossover study will enroll 32 healthy male subjects randomized 1:1 into two sequence groups (A/B, group A is administered in the sequence of T-R, while group B is in R-T). To evaluate the pharmacokinetic and pharmacodynamic properties of the test preparation and the control preparation in healthy male subjects. Each subject will receive single doses of both test and reference formulations across two periods (with ≥14-day washout), following the predefined sequence allocation table. After completing period 2 pharmacokinetic blood sampling, subjects will administer assigned insulin TID for two consecutive days to assess test-reference immunogenicity differences.

研究概览

研究类型

介入性

注册 (实际的)

32

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

    • Hubei
      • Wuhan、Hubei、中国、430000
        • 28 Baofeng Road, Qiaokou District

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. Age: 18 to 55 years old (inclusive of 18 and 55 years).
  2. Gender: Male.
  3. Body Weight: Not less than 55.0 kg for men, with a body mass index [BMI = weight (kg) / height² (m²)] between 18.0 and 29.0 kg/m² (inclusive of boundary values).
  4. Vital Signs: Systolic blood pressure ≥90 mmHg and <140 mmHg, diastolic blood pressure ≥60 mmHg and <90 mmHg, pulse rate ≥60 beats/min and ≤100 beats/min, body temperature (forehead) between 36.0°C and 37.3°C, with final judgment by the investigator.
  5. Glucose Tolerance: Normal glucose tolerance (fasting plasma glucose (FPG) <6.10 mmol/L and >3.50 mmol/L, and 2-hour postprandial blood glucose in oral glucose tolerance test (OGTT) <140 mg/dL (7.78 mmol/L)), glycated hemoglobin value <6.3% and >4.5%.

Exclusion Criteria:

  1. Those who have participated in a clinical trial of another drug/device and used the investigational drug/device within 6 months.
  2. Those with clinically significant abnormal conditions requiring exclusion, including but not limited to neurological, cardiovascular, hematologic and lymphatic, immune, renal, hepatic, gastrointestinal, respiratory, metabolic, and skeletal system disorders, particularly those with a history of hypoglycemia, hypokalemia, postural hypotension, syncope or blackout, diabetes mellitus, or a family history (first-degree relatives) of diabetes mellitus.
  3. Those with a history of severe vomiting, diarrhea, or any other disease or condition that could interfere with trial results within 7 days prior to the trial.
  4. Those with a history of specific allergies (e.g., asthma, urticaria, eczema) or allergies to any medications, foods, or pollen, or known allergies to insulin.
  5. Those with positive anti-insulin antibodies.
  6. Those who have lost or donated more than 400 mL of blood, received blood transfusions, or used blood products within 3 months prior to the trial, or who plan to donate blood during the trial.
  7. Subjects with plans for childbearing or sperm donation from 2 weeks prior to the trial to 6 months after the last dose, and who are unwilling or unable to use effective contraception.
  8. Those with clinically significant abnormalities in general physical examination, laboratory tests (blood routine, blood biochemistry, coagulation function, urine routine, etc.) within 7 days prior to the trial, or electrocardiogram results deemed clinically significant by the clinician within 14 days prior to the trial.
  9. Those with one or more clinically significant positive results for hepatitis B, hepatitis C, HIV, or syphilis tests.
  10. Those who have undergone surgery within 3 months prior to the trial, plan to undergo surgery during the study, or have had surgery that affects drug absorption, distribution, metabolism, or excretion.
  11. Those who consumed more than 14 units of alcohol per week within 3 months prior to the trial (1 unit = 17.7 mL ethanol, i.e., 354 mL of 5% alcohol beer, 44 mL of 40% alcohol liquor, or 147 mL of 12% alcohol wine), or those unable to abstain from alcohol during the trial.
  12. Those who smoked an average of more than 5 cigarettes per day within 3 months prior to the trial, or those unable to stop using any tobacco-based or nicotine products (e.g., nicotine patches, chewing gums) during the trial.
  13. Those who consumed excessive amounts of tea, coffee, and/or caffeine-rich beverages (more than 8 cups, 1 cup = 250 mL) per day within 3 months prior to the trial.
  14. Those who consumed any food or beverage rich in caffeine/xanthine or other special ingredients (e.g., strong tea, coffee, chocolate, cola, animal offal, grapefruit, grapefruit juice, dragon fruit, mango) from screening to 2 days before admission, which, in the investigator's judgment, may affect drug absorption, distribution, metabolism, or excretion, or those unable to stop consuming such foods or beverages by the end of drug administration.
  15. Those who used any drugs that alter liver enzyme activity within 28 days prior to the trial (common liver enzyme inducers: barbiturates (phenobarbital being the most common), carbamazepine, aminoglutethimide, griseofulvin, meprobamate, phenytoin, glutethimide, rifampicin, dexamethasone; common liver enzyme inhibitors: chlorpromazine, cimetidine, ciprofloxacin, metronidazole, chloramphenicol, sulfonamides).
  16. Those who used any drugs affecting insulin's glucose-lowering effects within 28 days prior to the trial (e.g., corticosteroids, danazol, diazoxide, diuretics, epinephrine, salbutamol, terbutaline, glucagon, growth hormone, thyroid hormone, beta-blockers).
  17. Those unable to eat, with swallowing difficulties, special dietary requirements, or unable to follow a standardized diet.
  18. Those who used any prescription drugs, over-the-counter drugs, nutraceuticals, herbal products, or vaccines within 14 days prior to the trial.
  19. Those engaged in hazardous mechanical operations, such as working at heights or driving motor vehicles.
  20. Those unable to tolerate venipuncture or with a history of hemophobia or needle phobia.
  21. Those with a history of asthma or seizures.
  22. Those with a history of hereditary galactose intolerance, lactase deficiency, or glucose-galactose malabsorption.
  23. ;Those who used any illicit drugs within one year prior to the trial.
  24. Those with a positive alcohol breath test or positive drug abuse screening.
  25. Subjects deemed by the investigator to have poor treatment compliance or any factors making participation in this trial inappropriate.

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:卫生服务研究
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:A组
a single subcutaneous dose of 0.3 IU/kg
a single subcutaneous dose of 0.3 IU/kg
有源比较器:B组
a single subcutaneous dose of 0.3 IU/kg
a single subcutaneous dose of 0.3 IU/kg

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
Primary PK Parameters (Peak Plasma Concentration (Cmax))
大体时间:0 to 12 hours
PK Parameters (Peak Plasma Concentration (Cmax))
0 to 12 hours
Primary PK Parameters (Area under the plasma concentration-time curve from time 0 to time τ(AUC0-τ))
大体时间:0 to 12 hours
Area under the plasma concentration-time curve from time 0 to time τ(AUC0-τ)
0 to 12 hours
Primary PD Parameters (Area under the glucose infusion rate curve from time 0 to time τ(AUCGIR0-τ))
大体时间:0 to 12 hours
Area under the glucose infusion rate curve from time 0 to time τ(AUCGIR0-τ)
0 to 12 hours
Primary PD Parameters (Maximum glucose infusion rate (GIRmax))
大体时间:0 to 12 hours
Maximum glucose infusion rate (GIRmax)
0 to 12 hours

次要结果测量

结果测量
措施说明
大体时间
Secondary PK Parameters (Area under the plasma concentration-time curve from time 0 to time 2 hours(AUC0-2h))
大体时间:0 to 2 hours
Area under the plasma concentration-time curve from time 0 to time 2 hours(AUC0-2h)
0 to 2 hours
Secondary PK Parameters (Area under the plasma concentration-time curve from time 0 extrapolated to infinity(AUC0-∞))
大体时间:0 to 12 hours
Area under the plasma concentration-time curve from time 0 extrapolated to infinity(AUC0-∞)
0 to 12 hours
Secondary PK Parameters (Time to maximum (peak) plasma concentration(Tmax))
大体时间:0 to 12 hours
Time to maximum (peak) plasma concentration(Tmax)
0 to 12 hours
Secondary PK Parameters (Terminal elimination rate constant(λz))
大体时间:0 to 12 hours
Terminal elimination rate constant(λz)
0 to 12 hours
Secondary PK Parameters (Elimination half-life(t1/2))
大体时间:0 to 12 hours
Elimination half-life(t1/2)
0 to 12 hours
Secondary PD Parameters (Area under the glucose infusion rate curve from time 0 to 2 hours(AUCGIR0-2h))
大体时间:0 to 2 hours
Area under the glucose infusion rate curve from time 0 to 2 hours(AUCGIR0-2h)
0 to 2 hours
Secondary PD Parameters (Time to reach maximum glucose infusion rate(TGIRmax))
大体时间:0 to 12 hours
Time to reach maximum glucose infusion rate(TGIRmax)
0 to 12 hours
Secondary PD Parameters (Time to onset of action,Tonset)
大体时间:0 to 12 hours
Time to onset of action,Tonset
0 to 12 hours

其他结果措施

结果测量
措施说明
大体时间
Immunogenicity Assessment (Anti-drug antibody (ADA) incidence (positive rate))
大体时间:0 to 12 hours
Anti-drug antibody (ADA) incidence (positive rate)
0 to 12 hours
Immunogenicity Assessment (ADA titers (for positive samples))
大体时间:0 to 12 hours
ADA titers (for positive samples)
0 to 12 hours

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4日

初级完成 (实际的)

2025年11月25日

研究完成 (实际的)

2026年1月13日

研究注册日期

首次提交

2026年5月5日

首先提交符合 QC 标准的

2026年5月19日

首次发布 (实际的)

2026年5月27日

研究记录更新

最后更新发布 (实际的)

2026年6月1日

上次提交的符合 QC 标准的更新

2026年5月27日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • PD-INS-PK-PD355

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

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