- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT05005065
Evaluation of the Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 in Healthy Caucasians
2022년 5월 10일 업데이트: 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.
연구 개요
상세 설명
[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
연구 유형
중재적
등록 (실제)
20
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 장소
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Seoul, 대한민국, 03080
- Seoul National University Hopsital
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Jongro Gu
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Seoul, Jongro Gu, 대한민국, 03080
- Seoul National University Hospital
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참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
19년 (성인)
건강한 자원 봉사자를 받아들입니다
예
연구 대상 성별
모두
설명
Inclusion Criteria:
- 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).
- Has ≥ 18.0 and ≤ 30.0 kg/m2 of body mass index (BMI) with a body weight (BW) ≥ 55.0 kg at screening.
- Has a negative result in serum Helicobacter pylori IgG antibody test.
- 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.
- 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:
- Has a history or current evidence of clinically significant disorder of hepatic, renal, nervous, respiratory, endocrine, hemato-oncologic, cardiovascular, urinary, and/or psychiatric system.
- 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).
- 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).
- Has a positive result on serology tests (for hepatitis B, human immunodeficiency virus [HIV], and hepatitis C).
- 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.
- Has a calculated eGFR per MDRD equation < 60 mL/min/1.73 m2 based on screening procedures including repeated ones.
- 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.
- 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.
- Has a history of drug abuse or has a positive response to drug abuse on urine drug screening test.
- 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).
- 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).
- 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.
- 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.
- Has a positive result for cotinine on urine drug screening test or is unable to stop smoking throughout the study.
- 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.
- 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.
- 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.
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)
- Is determined ineligible for study participation by the investigator for other reasons such as clinical laboratory abnormalities.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 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.
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Oral tablet
Oral capsule
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실험적: 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.
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Oral tablet
Oral capsule
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실험적: 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.
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Oral capsule
Oral capsule
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실험적: 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.
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Oral capsule
Oral capsule
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Cmax
기간: Day 1, Day 22
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PK: Maximum concentration of drug in plasma
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Day 1, Day 22
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AUClast
기간: Day 1, Day 22
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PK: Area under the plasma drug concentration-time curve from 0 to last point of measurable concentration
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Day 1, Day 22
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Cmax,ss
기간: Day 7 and Day 28
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PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
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Day 7 and Day 28
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AUCtau,ss
기간: Day 7 and Day 28
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PK: Area under the plasma drug concentration-time curve for a dosing interval at steady state
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Day 7 and Day 28
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Percent duration of pH ≥4 in 24 hrs (duration %)
기간: Day 1, Day 22
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PD: pH parameter
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Day 1, Day 22
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Percent duration of pH ≥4 in 24 hrs (duration %)
기간: Day 7, Day 28
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PD: pH parameter
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Day 7, Day 28
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Change from baseline in percent duration of pH ≥4 in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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AUCinf
기간: Day 1, Day 22
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PK: Area under the plasma drug concentration-time curve from time 0 to infinity
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Day 1, Day 22
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Tmax
기간: Day 1, Day 22
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PK: The time of peak concentration
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Day 1, Day 22
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t1/2
기간: Day 1, Day 22
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PK: Terminal half-life
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Day 1, Day 22
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CL/F
기간: Day 1, Day 22
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PK: Apparent Clearance
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Day 1, Day 22
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Vd/F
기간: Day 1, Day 22
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PK: Apparent volume of distribution after extravascular administration
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Day 1, Day 22
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Tmax,ss
기간: Day 7, Day 28
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PK: Time to reach Cmax
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Day 7, Day 28
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t1/2,ss
기간: Day 7, Day 28
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PK: Apparent first order terminal elimination half-life
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Day 7, Day 28
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Cmin,ss
기간: Day 7, Day 28
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PK: Minimum observed non zero concentration between dose time and dose time + dosing interval, tau
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Day 7, Day 28
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Cavg,ss
기간: Day 7, Day 28
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PK: The average concentration at steady state, calculated as the ratio of AUCtau to the dosing interval, tau
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Day 7, Day 28
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CLss/F
기간: Day 7, Day 28
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PK: The total body clearance at steady state after oral administration
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Day 7, Day 28
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Vd,ss/F
기간: Day 7, Day 28
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PK: Apparent volume of distribution after extravascular administration in steady state
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Day 7, Day 28
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PTF
기간: Day 7, Day 28
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PK: Peak to trough fluctuation
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Day 7, Day 28
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R
기간: Day 7, Day 28
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PK: Accumulation ratio
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Day 7, Day 28
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Percent duration of pH ≥3 in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Change from baseline in percent duration of pH ≥3 in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Percent duration of pH ≥6 in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Change from baseline in percent duration of pH ≥6 in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Mean and median pH in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Change from baseline in mean pH in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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Change from baseline in median pH in 24 hrs
기간: Day 1, Day 7, Day 22, Day 28
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PD: pH parameter
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Day 1, Day 7, Day 22, Day 28
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AUEGlast
기간: Day 1, Day 7, Day 22, Day 28
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PD(Gastrin): Area under the concentration-time curve of Serum Gastrin from 0 to last point of quantifiable concentration
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Day 1, Day 7, Day 22, Day 28
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Gmax
기간: Day 1, Day 7, Day 22, Day 28
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Gastrin: Maximum gastrin level
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Day 1, Day 7, Day 22, Day 28
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ΔAUEGlast
기간: Day 1, Day 7, Day 22, Day 28
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PD(Gastrin): Change from baseline in AUEGlast
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Day 1, Day 7, Day 22, Day 28
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ΔGmax
기간: Day 1, Day 7, Day 22, Day 28
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PD(Gastrin): Change from baseline in Gmax
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Day 1, Day 7, Day 22, Day 28
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
수사관
- 수석 연구원: In-Jin Jang, MD, Ph.D, Clinical Pharmacology and Therapeutics, Seoul National University Hospital
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (실제)
2021년 9월 6일
기본 완료 (실제)
2021년 11월 18일
연구 완료 (실제)
2021년 11월 30일
연구 등록 날짜
최초 제출
2021년 7월 5일
QC 기준을 충족하는 최초 제출
2021년 8월 6일
처음 게시됨 (실제)
2021년 8월 13일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2022년 5월 16일
QC 기준을 충족하는 마지막 업데이트 제출
2022년 5월 10일
마지막으로 확인됨
2021년 8월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- IN_BTK_102
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .