The Safety, Tolerability, and Pharmacokinetics of SYHX1901 Tablets in Chinese Healthy Subjects
NCT ID: NCT04880512
Last Updated: 2021-09-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1
102 participants
INTERVENTIONAL
2021-05-31
2022-12-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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SYHX 1901 tablets for SAD
Two subjects will be enrolled in a single dose group which is recommended as the initial dose. 8 out of 10 healthy subjects will be randomized to receive a single dose of SYHX 1901 tablets in fasted state.
SYHX 1901 tablets
SYHX 1901, oral tablets, in fasted state
Placebo for SAD
2 out of 10 healthy subjects will be randomized to receive a single dose of placebo in fasted state
Placebo
Matching placebo, oral tablets, in fasted state
SYHX 1901 tablets for MAD
8 out of 10 healthy subjects will be randomized to receive multiple doses of SYHX 1901 tablets in fasted state
SYHX 1901 tablets
SYHX 1901, oral tablets, in fasted state
Placebo for MAD
2 out of 10 healthy subjects will be randomized to receive multiple doses of placebo in fasted state
Placebo
Matching placebo, oral tablets, in fasted state
Interventions
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SYHX 1901 tablets
SYHX 1901, oral tablets, in fasted state
Placebo
Matching placebo, oral tablets, in fasted state
Eligibility Criteria
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Inclusion Criteria
2. Have a body mass index (BMI) between 18.0 and 26.0 kg/m2 (inclusive) and weigh at least 45.0 kg (female) or 50.0 kg (male) at screening；
3. Satisfactory medical assessment with no clinically significant or relevant abnormalities as determined by medical history, vital signs, physical examination, and clinical laboratory tests (hematology, urinalysis, and coagulation)；
4. Subjects and their partners agree to use effective n4. Subjects and their partners agree to use effective non-hormonal contraceptive measures (e.g., condoms, inert intrauterine devices, female barriers (cervix cap or diaphragm with spermicide), vaginal contraceptive ring, etc.) from signing the informed consent form to 6 months after the end of the study, or have taken permanent contraceptive measures (e.g., bilateral fallopian tube ligation, vasectomy, etc.); male subjects have no sperm donation plan from signing the informed consent to 6 months after the end of the study, female subjects have no egg donation plan from signing the informed consent form to 6 months after the end of the study；
5. Subjects who fully understand the study, voluntarily participate in the trial and sign the informed consent form.
Exclusion Criteria
2. History of severe allergies, herpes zoster infection, or tuberculosis;
3. Those who have taken any prescription drugs, over-the-counter drugs, proprietary Chinese medicines, herbal medicines, vitamin dietary supplements and health products within 4 weeks before signing the informed consent, and those who use oral long-acting contraceptives or use embedded long-acting contraceptives；
4. Subjects with diseases affecting drug absorption, distribution, metabolism and excretion as judged by investigator (e.g., acute and chronic diarrhea, acute and chronic gastritis, etc.);
5. Surgery history within 6 months prior to signing the informed consent;
6. Subjects with surgery plan (including cosmetic surgery, dental surgery and oral surgery), or strenuous exercise plan (including physical contact sports or collision sports) during the trial period;
7. Subjects with any clinically significant abnormalities in ECG, QTcF interval greater than 450 ms (male) or 470 ms (female), or with a history of prolonged QTcF interval;
8. Subjects with one or more abnormalities in the vital signs at screening: ear temperature \>37.5ºC, pulse rate \>100 beats/min, systolic blood pressure ≥140 mmHg or \<90 mmHg, diastolic blood pressure \>90 mmHg or \<50 mmHg；
9. The white blood cell count, the absolute value of neutrophils and the absolute value of lymphocytes are below the lower limit or higher than the upper limit of the reference value, and the percentage of reticulocyte (RET) is below the lower limit of the reference value in routine blood tests at screening;
10. History of acute respiratory or systemic infections within 2 weeks before signing the informed consent;
11. Blood lost or donation more than 400 mL within 3 months before signing the informed consent;
12. Alcohol abuse: consumption of more than 14 units of alcohol per week within 4 weeks prior to signing the informed consent or positive test for Alcohol at screening；
13. Smoker: more than 5 cigarettes per day within 6 months prior to signing informed consent；
14. Habitual intake of excessive xanthine- or caffeine-containing food, beverages, or other factors, which may interfere the absorption, distribution, metabolism, or excretion of drugs, within 4 weeks prior to screening；
15. Subjects have participated in clinical trials of any drug or medical device within 3 months before signing the informed consent;
16. History of substance abuse within the 1 years prior to signing the informed consent, or positive test for drug abuse at screening；
17. Female subjects who are pregnant or lactating;
18. Anti-Mullerian hormone (female only) test results not within the reference range at screening;
19. Positive test for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (anti-HCV), Human immunodeficiency virus antibody (anti-HIV) or Treponema Pallidum antibody (Anti-TP) at screening；
20. Suspected or known allergy to the test drug or any ingredient in the test drug, or subjects with allergic constitution;
21. Not suitable for this trial as determined by the investigator.
18 Years
45 Years
ALL
Yes
Sponsors
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CSPC Ouyi Pharmaceutical Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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jing zhang, Medical PhD
Role: PRINCIPAL_INVESTIGATOR
Huashan Hospital
Locations
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Huashan Hospital of Fudan University
Shanghai, , China
Countries
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Central Contacts
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Facility Contacts
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ying hu, master
Role: primary
Other Identifiers
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SYHX1902-CSP-001
Identifier Type: -
Identifier Source: org_study_id