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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.

調査の概要

詳細な説明

[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

研究の種類

介入

入学 (実際)

20

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Seoul、大韓民国、03080
        • Seoul National University Hopsital
    • Jongro Gu
      • Seoul、Jongro Gu、大韓民国、03080
        • Seoul National University Hospital

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

19年~50年 (大人)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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
実験的: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
実験的: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
実験的: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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Cmax
時間枠:Day 1, Day 22
PK: Maximum concentration of drug in plasma
Day 1, Day 22
AUClast
時間枠: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
時間枠:Day 7 and Day 28
PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
Day 7 and Day 28
AUCtau,ss
時間枠: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 %)
時間枠:Day 1, Day 22
PD: pH parameter
Day 1, Day 22
Percent duration of pH ≥4 in 24 hrs (duration %)
時間枠:Day 7, Day 28
PD: pH parameter
Day 7, Day 28
Change from baseline in percent duration of pH ≥4 in 24 hrs
時間枠:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28

二次結果の測定

結果測定
メジャーの説明
時間枠
AUCinf
時間枠:Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from time 0 to infinity
Day 1, Day 22
Tmax
時間枠:Day 1, Day 22
PK: The time of peak concentration
Day 1, Day 22
t1/2
時間枠:Day 1, Day 22
PK: Terminal half-life
Day 1, Day 22
CL/F
時間枠:Day 1, Day 22
PK: Apparent Clearance
Day 1, Day 22
Vd/F
時間枠:Day 1, Day 22
PK: Apparent volume of distribution after extravascular administration
Day 1, Day 22
Tmax,ss
時間枠:Day 7, Day 28
PK: Time to reach Cmax
Day 7, Day 28
t1/2,ss
時間枠:Day 7, Day 28
PK: Apparent first order terminal elimination half-life
Day 7, Day 28
Cmin,ss
時間枠: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
時間枠: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
時間枠:Day 7, Day 28
PK: The total body clearance at steady state after oral administration
Day 7, Day 28
Vd,ss/F
時間枠:Day 7, Day 28
PK: Apparent volume of distribution after extravascular administration in steady state
Day 7, Day 28
PTF
時間枠:Day 7, Day 28
PK: Peak to trough fluctuation
Day 7, Day 28
R
時間枠:Day 7, Day 28
PK: Accumulation ratio
Day 7, Day 28
Percent duration of pH ≥3 in 24 hrs
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
AUEGlast
時間枠: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
時間枠:Day 1, Day 7, Day 22, Day 28
Gastrin: Maximum gastrin level
Day 1, Day 7, Day 22, Day 28
ΔAUEGlast
時間枠:Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in AUEGlast
Day 1, Day 7, Day 22, Day 28
ΔGmax
時間枠:Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in Gmax
Day 1, Day 7, Day 22, Day 28

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:In-Jin Jang, MD, Ph.D、Clinical Pharmacology and Therapeutics, Seoul National University Hospital

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2021年9月6日

一次修了 (実際)

2021年11月18日

研究の完了 (実際)

2021年11月30日

試験登録日

最初に提出

2021年7月5日

QC基準を満たした最初の提出物

2021年8月6日

最初の投稿 (実際)

2021年8月13日

学習記録の更新

投稿された最後の更新 (実際)

2022年5月16日

QC基準を満たした最後の更新が送信されました

2022年5月10日

最終確認日

2021年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • IN_BTK_102

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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いいえ

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いいえ

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