The Safety, Tolerability, and Pharmacokinetics of SYHX1901 Tablets in Chinese Healthy Subjects
2021年9月24日 更新者:CSPC Ouyi Pharmaceutical Co., Ltd.
A Double-blinded, Randomized, Placebo-controlled, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of SYHX1901 Tablets in Chinese Healthy Subjects
This is a phase I clinical trial to evaluate the safety, tolerability and pharmacokinetic characteristics of single ascending doses and multiple ascending doses of SYHX1901 tablets in Chinese healthy subjects
研究概览
详细说明
This study is a randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability and pharmacokinetic characteristics of single ascending doses (part 1) and multiple ascending doses (part 2) of SYHX1901 tablets in Chinese healthy subjects.
研究类型
介入性
注册 (预期的)
102
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:ying hu, master
- 电话号码:15021575058
- 邮箱:hyy1102030@163.com
学习地点
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Shanghai、中国
- 招聘中
- Huashan Hospital of Fudan University
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接触:
- ying hu, master
- 电话号码:15021575058
- 邮箱:hyy1102030@163.com
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-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 45年 (成人)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Male or female subjects aged 18 to 45 years (inclusive);
- 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;
- 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);
- 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;
- Subjects who fully understand the study, voluntarily participate in the trial and sign the informed consent form.
Exclusion Criteria:
- Prior neurological/ psychiatric, respiratory system, endocrine system, blood system, skeletal-muscular system diseases or liver and kidney dysfunction or other diseases that may affect the results of the study;
- History of severe allergies, herpes zoster infection, or tuberculosis;
- 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;
- 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.);
- Surgery history within 6 months prior to signing the informed consent;
- 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;
- 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;
- 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;
- 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;
- History of acute respiratory or systemic infections within 2 weeks before signing the informed consent;
- Blood lost or donation more than 400 mL within 3 months before signing the informed consent;
- 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;
- Smoker: more than 5 cigarettes per day within 6 months prior to signing informed consent;
- 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;
- Subjects have participated in clinical trials of any drug or medical device within 3 months before signing the informed consent;
- History of substance abuse within the 1 years prior to signing the informed consent, or positive test for drug abuse at screening;
- Female subjects who are pregnant or lactating;
- Anti-Mullerian hormone (female only) test results not within the reference range at screening;
- 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;
- Suspected or known allergy to the test drug or any ingredient in the test drug, or subjects with allergic constitution;
- Not suitable for this trial as determined by the investigator.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的: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.
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SYHX 1901, oral tablets, in fasted state
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安慰剂比较:Placebo for SAD
2 out of 10 healthy subjects will be randomized to receive a single dose of placebo in fasted state
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Matching placebo, oral tablets, in fasted state
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实验性的: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
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SYHX 1901, oral tablets, in fasted state
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安慰剂比较:Placebo for MAD
2 out of 10 healthy subjects will be randomized to receive multiple doses of placebo in fasted state
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Matching placebo, oral tablets, in fasted state
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Safety and tolerability of SYHX1901 tablets
大体时间:SAD: up to14 days after the dosing, MAD: up to 7 days after the last dosing
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The safety and tolerability of single or multiple doses of SYHX1901 tablets administered orally will be assessed by incidence and severity of adverse events (AEs), abnormalities in clinical laboratory assessments, ECGs, vital sign assessments, and physical exams.
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SAD: up to14 days after the dosing, MAD: up to 7 days after the last dosing
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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The PK of SYHX1901 following single-dose and multiple doses
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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Peak Plasma Concentration (Cmax) of SYHX1901 following single-dose and multiple doses
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Pre-dose and multiple timepoints up to 144 hours after the last dose
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The PK of SYHX1901 following single-dose and multiple doses
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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Area under the plasma concentration versus time curve (AUC) of SYHX1901 following single-dose and multiple doses
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Pre-dose and multiple timepoints up to 144 hours after the last dose
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The PK of SYHX1901 following single-dose and multiple doses
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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The concentration peak time of SYHX1901 following single-dose and multiple doses Concentration peak time The peak time of SYHX1901 concentration following single-dose |
Pre-dose and multiple timepoints up to 144 hours after the last dose
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The PK of SYHX1901 following single-dose and multiple doses
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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The half-time of SYHX1901 following single-dose and multiple doses The half - time of SYHX1901 following single-dose |
Pre-dose and multiple timepoints up to 144 hours after the last dose
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The PK of SYHX1901 following single-dose and multiple doses
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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The plasma clearance rate (CL)of SYHX1901 following single-dose and multiple doses
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Pre-dose and multiple timepoints up to 144 hours after the last dose
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Urine PK parameters
大体时间:Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Urine pharmacokinetic parameters: The Urine clearance rate (CLr)of SYHX1901
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Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Urine PK parameters
大体时间:Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Urine pharmacokinetic parameters: Cumulative excretion from time t1 to t2(Aet1-t2) Fecal pharmacokinetic parameters:Cumulative excretion from time t1 to t2 Urine pharmacokinetic parameters:cumulative excretion from time t1 to t2 |
Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Fecal PK parameters
大体时间:Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Fecal pharmacokinetic parameters: cumulative excretion from time t1 to t2(Aft1-t2)
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Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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Identification of Metabolites of SYHX1901
大体时间:Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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It is a prospective study aiming to characterize metabolites of 1901 in human plasma, urine and feces.
The metabolism profiles of 1901 and main metabolites will be build up.
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Pre-dose and multiple timepoints up to 144 hours after the dose(180 mg)
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PD indexes: the level of PSTATs in blood cells
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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Pharmacodynamic indexes: the level of PSTATs in blood cells
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Pre-dose and multiple timepoints up to 144 hours after the last dose
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PD indexes: the inhibition rate of PSTATs in blood cells
大体时间:Pre-dose and multiple timepoints up to 144 hours after the last dose
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Pharmacodynamic indexes: the inhibition rate of PSTATs in blood cells
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Pre-dose and multiple timepoints up to 144 hours after the last dose
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:jing zhang, Medical PhD、Huashan Hospital
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年5月31日
初级完成 (预期的)
2022年8月20日
研究完成 (预期的)
2022年12月20日
研究注册日期
首次提交
2021年4月27日
首先提交符合 QC 标准的
2021年5月6日
首次发布 (实际的)
2021年5月10日
研究记录更新
最后更新发布 (实际的)
2021年9月30日
上次提交的符合 QC 标准的更新
2021年9月24日
最后验证
2021年9月1日
更多信息
与本研究相关的术语
其他研究编号
- SYHX1902-CSP-001
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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