A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and the Effect of Food of SYH2056 in Healthy Subjects
2026년 9월 8일 업데이트: InnovStone Therapeutics Limited
A Randomized, Double-Blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Food-Effect of SYH2056 Tablets in Healthy Subjects
This is a single-center, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK characteristics, and food effect of single ascending oral doses of SYH2056 tablets in healthy participants.
The study is planned to have two Parts: Part 1 [the single ascending dose (SAD) study] and Part 2 (the food effect study).
연구 개요
상태
상태
아직 모집하지 않음
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
중재적
등록 (추정된)
등록
72
단계
단계
- 1단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
연구 연락처
- 이름: Clinical Trials Information Group officer
- 전화번호: 031169085587
- 이메일: ctr-contact@cspc.cn
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
자격 기준
공부할 수 있는 나이
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건강한 자원 봉사자를 받아들입니다
예
설명
Inclusion Criteria:
Participants must meet all of the following criteria to be enrolled in this study:
- Age from 18 to 55 years (inclusive).
- Male or female, with the proportion of either sex being no less than 1/3.
- Weight ≥45.0 kg (females) or ≥50.0 kg (males), and body mass index (BMI) within the range of 18.0 to 26.0 kg/m2 (inclusive).
- Results of vital signs, physical examination, 12-lead ECG, laboratory tests, chest X-ray, B-mode ultrasound (liver, gallbladder, spleen, pancreas, kidneys), thyroid function test, etc., are normal or abnormal but not clinically significant as judged by the investigator.
- The participate and their partner agree to use effective non-hormonal contraceptive methods (e.g., condom, inert intrauterine device, female barrier methods [cervical cap or diaphragm with spermicide], vaginal ring, etc.) from signing the ICF until 3 months after the last dose, or have undergone permanent sterilization (e.g., bilateral tubal ligation, vasectomy, etc.). The participate has no plans to donate sperm or eggs from signing the ICF until 3 months after the end of the study.
- Participates must able to read and understand the written informed consent containing study-related information, fully understand the study content, procedures, and possible adverse reactions, voluntarily participate in the clinical study, sign the written ICF, and comply with the study procedures.
Exclusion Criteria:
A participate will not be eligible for inclusion in this study if any of the following criteria apply:
- Participates with history of clinically significant neurological, psychiatric, pulmonary, endocrine, hematological, musculoskeletal, gastrointestinal, cardiovascular, hepatic or renal diseases, or other diseases that might affect the study results or participants' safety as deemed by the investigator or designee.
- Participates with history of neuropsychiatric disorders, including current or past history of mental illness, current or recent use of psychotropic drugs, or other mental or psychological conditions deemed unsuitable for enrollment by the investigator or designee.
- Participates with abnormal blood pressure, such as systolic blood pressure ≥140 mmHg or <90 mmHg; diastolic blood pressure ≥90 mmHg or <60 mmHg.
- Participates with abnormal renal function, such as serum creatinine (Scr) > upper limit of normal (ULN), or estimated glomerular filtration rate (eGFR) <90 mL/min/1.73m2 or ≥130 mL/min/1.73m2.
- Participates with history of severe drug or food allergies, or judged by the investigator to be potentially allergic to the investigational drug.
- Participates who have taken any prescription drugs, over-the-counter drugs, herbal medicines, vitamin/dietary supplements, or health products within 4 weeks before signing the ICF. Or those who are using long-acting oral contraceptives, long-acting contraceptive implants, or hormone-releasing intrauterine devices.
- Participates with history of diseases which could affect drug absorption, distribution, metabolism, or excretion (e.g., acute or chronic diarrhea or gastritis, gastrectomy, enterectomy, or cholecystectomy, etc., with the exception of appendectomy).
- Participates who have undergone any surgery within 6 months before signing the ICF, or those who plan to undergo surgery (including cosmetic surgery, dental operation, and oral surgery) during the study.
- Participates with QTcF interval >450 ms (males) or >470 ms (females), or those who have a history of QT interval prolongation.
- Participates who have experienced blood loss or blood donation exceeding 400 mL within 3 months before signing the ICF, or those who have received a blood transfusion or have used blood products.
- Regular alcohol consumption, defined as an average weekly alcohol intake >14 units of alcohol within the 3 months prior to signing the ICF (1 unit = 285 mL of beer, 25 mL of spirits or 150 mL of wine), or positive breath alcohol test, or unable to abstain from alcohol during the study.
- Participates who smoked ≥ 5 cigarettes per day within 6 months before signing the ICF, or who are unable to abstain from any tobacco products during the study.
- Participates with habitual excessive consumption of foods, fruits, or beverages containing purines, caffeine, or grapefruit and grapefruit juice, or other foods that may affect drug absorption, distribution, metabolism, or excretion, within 2 weeks before dosing, such as coffee (>1,100 mL/day), tea (>2,200 mL/day), cola (>2,200 mL/day), energy drinks (>1,100 mL/day) and chocolate (>510 g/day).
- Participates who have enrolled in any clinical studies of drug or medical device within 3 months before signing the ICF.
- Participates with history of drug abuse within 1 year before signing the ICF, or who have a positive drug test as screening.
- Female participates with a positive pregnancy test at screening or who is lactating.
- Participates who have positive results in one or more of the following examinations: hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, anti-human immunodeficiency virus (HIV) antibody, or anti-Treponema pallidum-specific antibody.
- Participates with history of needle or blood phobia, or those who have difficulty with venous blood collection or can't tolerate venipuncture for other reasons.
- Participates with special dietary requirements and cannot accept the standardized diet and schedule.
- Any other factors that the investigator deems unsuitable for participation in the study.
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: 병렬 할당
- 마스킹: 삼루타
팔의 수
9
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: Group 1: SYH2056 dose1
Drug: SYH2056 tablets, dose1 on Day1 Other: Placebo matching dose1 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 2: SYH2056 dose2
Drug: SYH2056 tablets, dose2 on Day1 Other: Placebo matching dose2 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 3: SYH2056 dose3
Drug: SYH2056 tablets, dose3 on Day1 Other: Placebo matching dose3 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 4: SYH2056 dose4
Drug: SYH2056 tablets, dose4 on Day1 Other: Placebo matching dose4 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 5: SYH2056 dose5
Drug: SYH2056 tablets, dose5 on Day1 Other: Placebo matching dose5 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 6: SYH2056 dose6
Drug: SYH2056 tablets, dose6 on Day1 Other: Placebo matching dose6 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 7: SYH2056 dose7
Drug: SYH2056 tablets, dose7 on Day1 Other: Placebo matching dose7 on Day1
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
Placebo Comparator, taken matching the dosage of arm1 to arm7 on day1
|
|
실험적: Group 8: SYH2056 dose8
Drug: SYH2056 tablets with or without food, dose8 on Day1 or on Day5
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
|
|
실험적: Group 9: SYH2056 dose9
Drug: SYH2056 tablets with or without food, dose9 on Day1 or on Day5
|
SYH2056 tablets, 2mg/tablet or 8mg/tablet, [WQQ1.1]taken
according to the dosage of arm1 to arm7 on day1 SYH2056 tablets, 8mg/tablet, taken according to the dosage of arm8 and arm9 on day1 or say5
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Adverse events assessments
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Incidence, severity, seriousness, and relationship of treatment-emergent adverse events (TEAEs) will be assessed by CTCAE V5.0
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Changes in Systolic and Diastolic Blood Pressure Blood Pressure
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Changes in systolic and diastolic blood pressure will be assessed during the study(Unit: mmHg)
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Changes in Pulse Rate
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Changes in pulse rate will be assessed during the study(Unit: beats/min)
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Changes in Body Temperature
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Changes in body temperature will be assessed during the study(Unit: °C)
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Incidence of Clinically Significant Abnormal Findings in Physical Examination
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Clinically significant abnormalities identified by physical examination, including general condition, skin and mucous membranes, superficial lymph nodes, head, neck, thyroid, chest (including thorax, lungs, and heart), abdomen, spine/limbs, and nervous system examinations, will be assessed during the study.
The results will be presented as the percentage of participants (%) with clinically significant abnormalities
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Clinically Significant Abnormal Findings in Hematology Tests
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Clinically significant abnormalities identified by hematology tests, including complete blood count parameters, will be assessed during the study.
The results will be presented as the percentage of participants(%) with clinically significant abnormalitiesClinically significant abnormalities identified by hematology tests, including complete blood count parameters, will be assessed during the study.
The results will be presented as the percentage of participants(%) with clinically significant abnormalities
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Clinically Significant Abnormal Findings in Blood Biochemistry Tests
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Clinically significant abnormalities identified by blood biochemistry tests, including liver function, renal function, and metabolic parameters, will be assessed during the study.
The results will be presented as the percentage of participants(%) with clinically significant abnormalities
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Clinically Significant Abnormal Findings in Coagulation Tests
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Clinically significant abnormalities identified by coagulation tests, including coagulation parameters, will be assessed during the study.
The results will be presented as the percentage of participants(%) with clinically significant abnormalities
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Clinically Significant Abnormal Findings in Urinalysis
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Clinically significant abnormalities identified by urinalysis, including urine parameters, will be assessed during the study.
The results will be presented as the percentage of participants(%) with clinically significant abnormalities
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
12-lead electrocardiograms (ECGs)
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Changes in 12-lead electrocardiogram parameters, including heart rate, PR interval, QRS interval, QT interval, and QTc interval, will be assessed
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Modified Observer's Assessment of Alertness/Sedation (MOAA/S) Score
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Potential effects of SYH2056 on neuropsychiatric status will be assessed by the MOAA/S Score.
The MOAA/S score ranges from 0 to 5, with higher scores indicating a higher level of alertness (less sedation) and lower scores indicating a deeper level of sedation.
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Columbia Suicide Severity Rating Scale (C-SSRS) Assessed
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Potential effects of SYH2056 on neuropsychiatric status will be assessed by the C-SSRS.
Suicidal ideation severity is rated from 0 to 5, with higher scores indicating greater severity of suicidal ideation.
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Clinician-Administered Dissociative States Scale (CADSS)
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Hallucinogenic properties of SYH2065 will be assessed by the CADSS.
The CADSS total score ranges from 0 to 92, with higher scores indicating greater severity of dissociative symptoms.
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
Brief Psychiatric Rating Scale (BPRS)
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Hallucinogenic properties of SYH2065 will be assessed by the BPRS.
The BPRS total score ranges from 18 to 126, with higher scores indicating greater severity of psychiatric symptoms.
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
the Physician Withdrawal Checklist 20 (PWC-20)
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Subject's subjective liking of SYH2065 will be assessed by the PWC-20
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
The Drug Liking Visual Analogue Scale (VAS)
기간: Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
Subject's subjective liking of SYH2065 will be assessed by the VAS.
The score ranges from 0 to 100, with higher scores indicating greater subjective liking of the drug.
|
Up to Day11 for Part1 SAD study, up to Day15 for Part2 FE study
|
|
t1/2
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Elimination Half-Life of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
Tmax
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Time to Peak Concentration of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
Cmax
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Maximum Plasma Concentration of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
AUC0-t
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Area under the Drug Concentration-Time Curve from Time 0 to the Last Measurable Time Point of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
AUC0-inf
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Area under the Drug Concentration-Time Curve from Time 0 to Infinity of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
CL/F
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Apparent Volume of Distribution of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
Vz/F
기간: Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
Apparent Volume of Distribution of SYH2056
|
Day1 to Day4 for Part1 SAD study, Day1 to Day8 for Part2 FE study
|
|
SYH2056 Metabolites
기간: Up to Day11 for Part1 SAD study
|
Identification of SYH2056 metabolites in plasma and urine, and to characterize its metabolic pathways
|
Up to Day11 for Part1 SAD study
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
협력자
협력자
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 (추정된)
연구 시작
2026년 8월 30일
기본 완료 (추정된)
기본 완료
2027년 1월 30일
연구 완료 (추정된)
연구 완료
2027년 3월 30일
연구 등록 날짜
최초 제출
최초 제출
2026년 5월 14일
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
2026년 8월 14일
처음 게시됨 (실제)
처음 게시됨
2026년 8월 18일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
2026년 9월 9일
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
2026년 9월 8일
마지막으로 확인됨
마지막으로 확인됨
2026년 8월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
기타 연구 ID 번호
- SYH2056-001
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
아니
미국 FDA 규제 기기 제품 연구
아니
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