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健康受试者中HRS-1893片剂两种制剂的生物等效性研究

2026年9月18日 更新者:Shandong Suncadia Medicine Co., Ltd.

健康受试者中两种HRS-1893片剂配方的生物等效性研究

This study will investigate the bioequivalence between two formulations of HRS-1893 tablets. Safety and tolerability will also be assessed.

研究概览

研究类型

介入性

注册 (实际的)

58

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

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100730
        • Beijing Hospital

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 至 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Subjects aged 18 to 55 years (inclusive), regardless of gender;
  2. Body mass index (BMI) between 19 and 28 kg/m² (inclusive), with body weight ≥ 50.0 kg and < 90.0 kg for men, and ≥ 45.0 kg and < 90.0 kg for women;
  3. No abnormalities of clinical significance are found upon comprehensive physical examination and laboratory tests, or only minor abnormalities that are deemed by the investigator not to affect the subject's eligibility for enrollment;
  4. No clinically significant abnormalities on the 12-lead ECG;
  5. The subject must understand the study procedures and methods, voluntarily agree to participate, and provide written informed consent.

Exclusion Criteria:

  1. Subjects with suspected hypersensitivity to the investigational drug or any excipient;
  2. The subject has a history of syncope;
  3. Exclusion due to blood pressure: Systolic Blood Pressure (SBP) >140 mmHg or <90 mmHg; OR Diastolic Blood Pressure (DBP) >90 mmHg or <60 mmHg, as determined by the investigator to be clinically significant;
  4. History of gastric or intestinal surgery that, in the investigator's judgment, may affect drug absorption;
  5. A positive result in any one of the following infectious disease screening tests during the screening period: hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV-Ab), treponema pallidum antibody (syphilis), or human immunodeficiency virus antibody/antigen (HIV-Ab/Ag);
  6. Subjects who meet any of the following criteria will be excluded: a. Smoking: Average daily cigarette consumption of more than 5 cigarettes within the 4 weeks prior to screening; b. Alcohol: Average daily alcohol intake exceeding 15 g within one week prior to screening (15 g of alcohol is equivalent to 450 mL of beer, 150 mL of wine, or 50 mL of low-alcohol spirits); c. Non-compliance: Inability or unwillingness to abstain from smoking, alcohol, and caffeine-containing foods or beverages during the screening period and the entire study duration; d. Diet: Have special dietary requirements, cannot comply with the standardized diet provided in the study, or have a history of substance abuse;
  7. History of substance abuse;
  8. Use of any prescription drugs, over-the-counter medications, or Chinese herbal medicines within 1 month prior to dosing, or the use of any drug within 5 half-lives prior to screening (whichever is longer). Additionally, subjects who plan to take any non-study medications during the trial period will be excluded;
  9. Any other circumstances that, in the investigator's judgment, make the subject unsuitable for participation in the trial. This includes physiological or psychological conditions that may increase the trial risk, affect the subject's protocol compliance, or impact the subject's ability to complete the 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:治疗
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:HRS-1893测试制剂组

Test formulation of HRS-1893 tablet, oral.

实验性的:HRS-1893 参比制剂组

Reference formulation of HRS-1893 tablet, oral.

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
Peak concentration (Cmax).
大体时间:From Day 1 to Day 17.

Primary Pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Area under the plasma concentration - time curve from Time 0 to the last quantifiable time point (AUC0-t).
大体时间:From Day 1 to Day 17.

Primary Pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Area under the plasma concentration - time curve from Time 0 to infinity (AUC0-∞).
大体时间:From Day 1 to Day 17.

Primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.

次要结果测量

结果测量
措施说明
大体时间
Time to peak concentration (Tmax).
大体时间:From Day 1 to Day 17.

Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Elimination half-life (t1/2).
大体时间:From Day 1 to Day 17.

Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Apparent clearance (CL/F).
大体时间:From Day 1 to Day 17.

Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Apparent volume of distribution (Vz/F).
大体时间:From Day 1 to Day 17.

Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 17.
Incidence and severity of any adverse events (AEs).
大体时间:From Day 1 to Day 21 ± 2.

Safety and tolerability of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 21 ± 2.
12-Lead Electrocardiogram (ECG) QT Interval.
大体时间:From Day 1 to Day 21 ± 2.

Safety and tolerability of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 21 ± 2.
Transthoracic echocardiogram (TTE) results.
大体时间:From Day 1 to Day 21 ± 2.

Safety and tolerability of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 21 ± 2.
Vital signs results - blood pressure.
大体时间:From Day 1 to Day 21 ± 2.

Safety and tolerability of different HRS-1893 formulations in healthy subjects.

From Day 1 to Day 21 ± 2.

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)

2026年4月14日

初级完成 (实际的)

2026年9月14日

研究完成 (实际的)

2026年9月14日

研究注册日期

首次提交

2026年3月11日

首先提交符合 QC 标准的

2026年3月15日

首次发布 (实际的)

2026年3月18日

研究记录更新

最后更新发布 (实际的)

2026年9月21日

上次提交的符合 QC 标准的更新

2026年9月18日

最后验证

2026年9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

  • HRS-1893-108

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

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