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。

Evaluation of the Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 in Healthy Caucasians

2022年5月10日 更新者:HK inno.N Corporation

A Randomized, Open-label, Multiple Dosing, Cross-over Phase 1 Clinical Trial to Evaluate Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 After Oral Administration in Healthy Caucasian Subjects

The purpose of this study is to evaluate pharmacokinetics/pharmacodynamics and safety/tolerability of IN-C005 and IN-A001 after oral administration in healthy Caucasian subjects.

研究概览

详细说明

[Part 1] To evaluate the pharmacokinetic (PK)/pharmacodynamic (PD) profiles and safety/tolerability of 100 mg IN-C005 versus 100 mg IN-A001 after multiple oral dosing in healthy Caucasian subjects

[Part 2] To evaluate the PK/PD profiles and safety/tolerability of 50 mg IN-C005 versus 75 mg IN-C005 after multiple oral dosing in healthy Caucasian subjects

研究类型

介入性

注册 (实际的)

20

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

      • Seoul、大韩民国、03080
        • Seoul National University Hopsital
    • Jongro Gu
      • Seoul、Jongro Gu、大韩民国、03080
        • Seoul National University 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

19年 至 50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. Is healthy Caucasian adult aged 19 to 50 years (inclusive) at the time of signing the informed consent form (ICF) (A Caucasian is defined as a European who was born in Europe, has the duration of residence outside of Europe less than 10 years, and both of whose parents and grandparents are European-born).
  2. Has ≥ 18.0 and ≤ 30.0 kg/m2 of body mass index (BMI) with a body weight (BW) ≥ 55.0 kg at screening.
  3. Has a negative result in serum Helicobacter pylori IgG antibody test.
  4. Decides to participate voluntarily in the study after being fully informed of and understanding the study completely, and provides his/her written informed consent prior to screening procedure.
  5. Is eligible for this study in the opinion of the investigator based on the results of physical examination, clinical laboratory tests, interview, etc.

Exclusion Criteria:

  1. Has a history or current evidence of clinically significant disorder of hepatic, renal, nervous, respiratory, endocrine, hemato-oncologic, cardiovascular, urinary, and/or psychiatric system.
  2. Has a history or current evidence of gastrointestinal disease that may affect the safety and PD assessments for study treatment (e.g., gastrointestinal ulcer, gastritis, gastric cramp, gastroesophageal reflux disease, and Crohn's disease) or a history of gastrointestinal surgery (except for simple appendectomy or herniotomy).
  3. Has a history or current evidence of clinically significant hypersensitivity to study drugs or any ingredient of proton pump inhibitors and other drugs (such as aspirin and antibiotics).
  4. Has a positive result on serology tests (for hepatitis B, human immunodeficiency virus [HIV], and hepatitis C).
  5. Has a blood level of total bilirubin, AST (GOT), or ALT (GPT) > 1.5 X upper limit of normal (ULN) based on screening procedures including repeated ones.
  6. Has a calculated eGFR per MDRD equation < 60 mL/min/1.73 m2 based on screening procedures including repeated ones.
  7. Has systolic blood pressure (SBP) of < 90 mmHg or > 140 mmHg, diastolic blood pressure (DBP) of < 50 mmHg or > 95 mmHg, or pulse rate (PR) of < 45 beats/min or > 100 beats/min on vital signs as measured in sitting position after taking a rest for at least 5 minutes at screening.
  8. Has an anatomical disorder that precludes insertion and maintenance of intragastric pH meter catheter or is expected to be intolerable to insertion of intragastric pH meter catheter.
  9. Has a history of drug abuse or has a positive response to drug abuse on urine drug screening test.
  10. Has received any prescription drug or herbal medication within 2 weeks of or any over-the-counter (OTC) drug, dietary supplements, or vitamins within 1 week of scheduled first dose or is expected to receive such medication during the study (Note: a subject may participate in the study at the discretion of the investigator provided the subject meets all the other criteria).
  11. Has participated and received an investigational agent in another clinical trial or bioequivalence study within 6 months prior to the first dose of study treatment (Note: This is not applied to participation in another part of this study).
  12. Has donated whole blood within 2 months prior to the scheduled first dose, or has donated blood components or received transfusion within a month prior to the scheduled first dose.
  13. Has excessive caffeine intake (> 5 units/day), continues the use of alcohol (> 21 units/week, 1 unit = 10 g of pure alcohol), or is unable to stop drinking during hospitalization period.
  14. Has a positive result for cotinine on urine drug screening test or is unable to stop smoking throughout the study.
  15. Is unable to avoid grapefruit-containing foods during the time from 24 hours (hrs) before hospitalization to discharge in Period 1 and Period 2, respectively.
  16. Is unable to avoid caffeine-containing foods (e.g., coffee, tea [red tea, green tee, etc.], soda, coffee milk, and nutritive tonic drink) during the time from 24 hrs before hospitalization to discharge Period 1 and Period 2, respectively.
  17. For all women of childbearing potential (WOCBP) excluding those on amenorrhea for at least 12 months and those who underwent surgical sterilization (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy), has a positive result for pregnancy test (urine hCG) performed prior to the first dose of study treatment or is pregnant or breastfeeding.
  18. Is unable to use a medically acceptable contraceptive method throughout the study. Medically acceptable contraceptive methods include:

    • Use of an intrauterine device with a proven birth control failure rate by the subject or subject's spouse (or partner)
    • Use of (male or female) barrier method with spermicide
    • Surgical sterilization (vasectomy, salpingectomy, tubal ligation, hysterectomy) of the subject or subject's spouse (or partner)
  19. Is determined ineligible for study participation by the investigator for other reasons such as clinical laboratory abnormalities.

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:Treatment AB
Participants will be randomized to receive IN-C005 Y mg (Treatment A) and IN-A001 Y mg (Treatment B) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
实验性的:Treatment BA
Participants will be randomized to receive IN-A001 Y mg and IN-C005 Y mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
实验性的:Treatment CD
Participants will be randomized to receive IN-C005 Z mg (Treatment C) and IN-C005 X mg (Treatment D) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule
实验性的:Treatment DC
Participants will be randomized to receive IN-C005 X mg and IN-C005 Z mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule

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
Cmax
大体时间:Day 1, Day 22
PK: Maximum concentration of drug in plasma
Day 1, Day 22
AUClast
大体时间:Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from 0 to last point of measurable concentration
Day 1, Day 22
Cmax,ss
大体时间:Day 7 and Day 28
PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
Day 7 and Day 28
AUCtau,ss
大体时间:Day 7 and Day 28
PK: Area under the plasma drug concentration-time curve for a dosing interval at steady state
Day 7 and Day 28
Percent duration of pH ≥4 in 24 hrs (duration %)
大体时间:Day 1, Day 22
PD: pH parameter
Day 1, Day 22
Percent duration of pH ≥4 in 24 hrs (duration %)
大体时间:Day 7, Day 28
PD: pH parameter
Day 7, Day 28
Change from baseline in percent duration of pH ≥4 in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28

次要结果测量

结果测量
措施说明
大体时间
AUCinf
大体时间:Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from time 0 to infinity
Day 1, Day 22
Tmax
大体时间:Day 1, Day 22
PK: The time of peak concentration
Day 1, Day 22
t1/2
大体时间:Day 1, Day 22
PK: Terminal half-life
Day 1, Day 22
CL/F
大体时间:Day 1, Day 22
PK: Apparent Clearance
Day 1, Day 22
Vd/F
大体时间:Day 1, Day 22
PK: Apparent volume of distribution after extravascular administration
Day 1, Day 22
Tmax,ss
大体时间:Day 7, Day 28
PK: Time to reach Cmax
Day 7, Day 28
t1/2,ss
大体时间:Day 7, Day 28
PK: Apparent first order terminal elimination half-life
Day 7, Day 28
Cmin,ss
大体时间:Day 7, Day 28
PK: Minimum observed non zero concentration between dose time and dose time + dosing interval, tau
Day 7, Day 28
Cavg,ss
大体时间:Day 7, Day 28
PK: The average concentration at steady state, calculated as the ratio of AUCtau to the dosing interval, tau
Day 7, Day 28
CLss/F
大体时间:Day 7, Day 28
PK: The total body clearance at steady state after oral administration
Day 7, Day 28
Vd,ss/F
大体时间:Day 7, Day 28
PK: Apparent volume of distribution after extravascular administration in steady state
Day 7, Day 28
PTF
大体时间:Day 7, Day 28
PK: Peak to trough fluctuation
Day 7, Day 28
R
大体时间:Day 7, Day 28
PK: Accumulation ratio
Day 7, Day 28
Percent duration of pH ≥3 in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥3 in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Percent duration of pH ≥6 in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥6 in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Mean and median pH in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in mean pH in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in median pH in 24 hrs
大体时间:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
AUEGlast
大体时间:Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Area under the concentration-time curve of Serum Gastrin from 0 to last point of quantifiable concentration
Day 1, Day 7, Day 22, Day 28
Gmax
大体时间:Day 1, Day 7, Day 22, Day 28
Gastrin: Maximum gastrin level
Day 1, Day 7, Day 22, Day 28
ΔAUEGlast
大体时间:Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in AUEGlast
Day 1, Day 7, Day 22, Day 28
ΔGmax
大体时间:Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in Gmax
Day 1, Day 7, Day 22, Day 28

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。

调查人员

  • 首席研究员:In-Jin Jang, MD, Ph.D、Clinical Pharmacology and Therapeutics, Seoul National University Hospital

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)

2021年9月6日

初级完成 (实际的)

2021年11月18日

研究完成 (实际的)

2021年11月30日

研究注册日期

首次提交

2021年7月5日

首先提交符合 QC 标准的

2021年8月6日

首次发布 (实际的)

2021年8月13日

研究记录更新

最后更新发布 (实际的)

2022年5月16日

上次提交的符合 QC 标准的更新

2022年5月10日

最后验证

2021年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • IN_BTK_102

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