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A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and the Effect of Food of SYH2056 in Healthy Subjects

8 september 2026 uppdaterad av: 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).

Studieöversikt

Status

Har inte rekryterat ännu

Betingelser

Studietyp

Interventionell

Inskrivning (Beräknad)

72

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Clinical Trials Information Group officer
  • Telefonnummer: 031169085587
  • E-post: ctr-contact@cspc.cn

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

Participants must meet all of the following criteria to be enrolled in this study:

  1. Age from 18 to 55 years (inclusive).
  2. Male or female, with the proportion of either sex being no less than 1/3.
  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).
  4. 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.
  5. 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.
  6. 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:

  1. 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.
  2. 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.
  3. Participates with abnormal blood pressure, such as systolic blood pressure ≥140 mmHg or <90 mmHg; diastolic blood pressure ≥90 mmHg or <60 mmHg.
  4. 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.
  5. Participates with history of severe drug or food allergies, or judged by the investigator to be potentially allergic to the investigational drug.
  6. 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.
  7. 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).
  8. 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.
  9. Participates with QTcF interval >450 ms (males) or >470 ms (females), or those who have a history of QT interval prolongation.
  10. 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.
  11. 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.
  12. 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.
  13. 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).
  14. Participates who have enrolled in any clinical studies of drug or medical device within 3 months before signing the ICF.
  15. Participates with history of drug abuse within 1 year before signing the ICF, or who have a positive drug test as screening.
  16. Female participates with a positive pregnancy test at screening or who is lactating.
  17. 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.
  18. 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.
  19. Participates with special dietary requirements and cannot accept the standardized diet and schedule.
  20. Any other factors that the investigator deems unsuitable for participation in the study.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Trippel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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
Experimentell: 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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Adverse events assessments
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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
Tidsram: 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
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Clinician-Administered Dissociative States Scale (CADSS)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

30 augusti 2026

Primärt slutförande (Beräknad)

30 januari 2027

Avslutad studie (Beräknad)

30 mars 2027

Studieregistreringsdatum

Först inskickad

14 maj 2026

Först inskickad som uppfyllde QC-kriterierna

14 augusti 2026

Första postat (Faktisk)

18 augusti 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

8 september 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • SYH2056-001

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