此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Pharmacokinetics of Huperzine A Oral Solution in Healthy Participants

2026年8月20日 更新者:Wanbangde Pharmaceutical Group Co., LTD

A Single-Center, Randomized, Double-Blind, Multiple-Dose, Dose-Escalation Study to Evaluate the Pharmacokinetics of Huperzine A Oral Solution in Healthy Participants

In this study, 4 dose groups are planned: Group 1 (0.22 mg, QD), Group 2 (0.22 mg, BID), Group 3 (0.44 mg, QD), and Group 4 (0.44 mg, BID). Ten healthy study participants will be enrolled in each dose group, and randomized to the investigational drug group or the placebo group in a 4:1 ratio (i.e., 8 study participants in the investigational drug group and 2 study participants in the placebo group). An appropriate gender ratio will be ensured within each dose group.

研究概览

地位

尚未招聘

条件

研究类型

介入性

注册 (估计的)

40

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

学习地点

    • Zhejiang
      • Wenzhou、Zhejiang、中国
        • The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
        • 接触:

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

  • 成人

接受健康志愿者

是的

描述

Inclusion Criteria:

  1. Participants must provide written informed consent prior to the study, with full understanding of the study's objectives, procedures, and potential adverse reactions;
  2. Participants must be able to communicate effectively with the investigators and comply with the protocol requirements throughout the study.
  3. Healthy male or female, aged 18 to 55 years (inclusive);
  4. Body mass index (BMI) range: 19.0 to 26.0 kg/m2 [BMI = body weight/height2 (kg/m2)] (inclusive); male weight ≥50 kg, female weight ≥45 kg.

Exclusion Criteria:

  1. History of allergy to huperzine A or any drug component (pharmaceutical-grade sodium benzoate); history of allergies to two or more drugs, foods, etc.;
  2. History or suspected history of gastrointestinal bleeding, or conditions posing a risk of gastrointestinal bleeding (e.g., peptic ulcer, inflammatory bowel disease, diverticula, hemorrhoids, colonic polyps, etc.);
  3. Currently diagnosed with or suspected of having epilepsy, angina pectoris, bronchial asthma, mechanical intestinal obstruction, renal insufficiency, or urinary tract obstruction;
  4. Currently diagnosed with or suspected of having other serious diseases that, in the judgment of the investigator, make the individual unsuitable for participation in the study. These may include, but are not limited to, diseases related to the respiratory, circulatory, digestive, hematologic, endocrine, immune, integumentary, neuropsychiatric, or otorhinolaryngologic systems;
  5. Underwent major surgery within 180 days prior to the first dose or plans to undergo surgery during the study period;
  6. Participants with significant abnormalities in vital signs (normal reference ranges for vital signs (including critical values): body temperature (aural) 35.9 ℃ to 37.4 ℃, sitting systolic blood pressure 90 mmHg to 140 mmHg, sitting diastolic blood pressure 60 mmHg to 90 mmHg, sitting pulse 50 to 100 beats per minute, respiratory rate 12 to 20 breaths per minute), physical examination, electrocardiogram (QT interval corrected for heart rate using Fridericia's formula (QTcF) >450 ms (males) or >460 ms (females)), or laboratory test results, and judged by the investigator as unsuitable for participation in this study;
  7. History of hepatitis B, hepatitis C, HIV, or syphilis and/or those with one or more abnormal results in infectious disease screening (anti-HIV antibody, hepatitis B surface antigen, anti-hepatitis C virus antibody, anti-Treponema pallidum antibody) that are considered clinically significant by the investigator;
  8. Study participants who have experienced blood loss (excluding normal physiological blood loss in females) or donated ≥200 mL of blood or donated blood components (e.g., plasma, platelets, peripheral blood stem cells, etc.) within 90 days prior to the first dose;
  9. Individuals who used any drugs that alter hepatic enzyme activity within 30 days prior to the first dose (e.g., inducers such as barbiturates, carbamazepine, phenytoin sodium, dexamethasone; inhibitors such as selective serotonin reuptake inhibitors [SSRIs], ciprofloxacin, diltiazem, macrolides, metronidazole, ketoconazole, verapamil, fluoroquinolones, etc.), or non-steroidal anti-inflammatory drugs (NSAIDs) (e.g., aspirin, ibuprofen, naproxen, etc.);
  10. Use of any medications (including prescription drugs, over-the-counter drugs, and herbal medicines) and health supplements within 14 days prior to the first dose or within 5 half-lives of previous medication (whichever is longer), with the exception of topical medications and ophthalmic drops intended for local use.
  11. Study participants who have been vaccinated within 30 days prior to the first dose or plan to be vaccinated within 30 days after the end of the study;
  12. Participation in any clinical study within 90 days prior to the first dose;
  13. History of drug abuse within 5 years prior to screening, and/or use of illicit drugs within 90 days prior to screening, and/or history of drug dependence, including herbal medicine, or positive urine drug screening;
  14. Average daily smoking of more than 5 cigarettes within 90 days prior to screening, or unwillingness to avoid using any tobacco products within 48 h prior to the first dose and during hospitalization, or positive result in nicotine screening;
  15. Regular alcohol consumption within 180 days prior to screening, defined as consuming more than 14 units of alcohol per week (1 unit of alcohol = 360 mL of beer or 45 mL of spirits or 150 mL of wine), or unwillingness to stop alcohol intake within 48 h prior to the first dose and during hospitalization, or positive result in alcohol breath test;
  16. Excessive daily consumption of tea, coffee, and/or caffeine-containing beverages (more than 8 cups, 1 cup = 250 mL) within 90 days prior to screening, or unwillingness to abstain from tea, coffee, and/or caffeine-containing foods, grapefruit (pomelo) and/or grapefruit juice (pomelo juice), and/or poppy-containing products within 48 h prior to the first dose and during hospitalization;
  17. Individuals who have plans for reproduction (including sperm or egg donation) from the time of signing the informed consent until 90 days after the last administration of the investigational product, and/or who do not agree to use effective non-pharmacological contraceptive methods during the study period;
  18. Individuals unable to adhere to a standardized diet during the study or those with lactose intolerance (e.g., experiencing diarrhea after consuming milk);
  19. Individuals with difficulty in venous blood collection (intolerance to venipuncture, history of needle or blood phobia, poor vascular condition, etc.);
  20. Individuals who are otherwise unable to complete the study or are deemed unsuitable for inclusion by the investigator shall also be excluded.

    In addition to the aforementioned criteria, female participants meeting any of the following conditions shall also be excluded:

  21. Currently pregnant or breastfeeding, or have a positive pregnancy test result;
  22. Use of oral contraceptives within 30 days prior to the first dose;
  23. Use of long-acting estrogen and/or progestin injections and/or implants within 180 days prior to the first dose;
  24. Unprotected sexual intercourse with a partner within 14 days prior to the first dose.

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:基础科学
  • 分配:随机化
  • 介入模型:顺序分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Huperzine A Oral Solution
Healthy participants receive multiple escalating oral doses of huperzine A oral solution in sequential cohorts. Advancement to subsequent dose cohorts is gated by review from the Safety Monitoring Committee (SMC) and Sponsor. Subjects within each cohort are randomized to study drug or placebo.
Investigational huperzine A oral solution, administered orally in 4 sequential escalating multiple-dose cohorts to healthy adult participants.
安慰剂比较:Placebo
Healthy participants receive matching placebo oral solution for multiple-dose administration. Randomization to placebo occurs within each sequential dose cohort, following SMC-gated cohort progression rules.
Matching placebo, identical in appearance, taste and packaging to huperzine A oral solution, administered orally for multiple doses.

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
Safety and Tolerability Assessments
大体时间:From first study drug administration through Day 9
Assess safety and tolerability by evaluating treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and clinically significant abnormal findings from vital signs, physical examinations, 12-lead ECG (QTcF, PR interval, QRS duration, RR interval), and clinical laboratory tests.
From first study drug administration through Day 9

次要结果测量

结果测量
大体时间
Time to Peak Plasma Concentration (Tmax)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Peak Plasma Concentration (Cmax)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Area Under the Plasma Concentration-Time Curve From Time Zero to Last Quantifiable Concentration (AUC0-t)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Area Under the Plasma Concentration-Time Curve From Time Zero Extrapolated to Infinite Time (AUC0-∞)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Area Under the Plasma Concentration-Time Curve Over One Dosing Interval (AUC0-τ)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Percentage of Area Under the Curve Extrapolated to Infinite Time (AUC_%Extrap)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Apparent Volume of Distribution Based on Terminal Phase (Vz/F)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Apparent Total Clearance Based on Terminal Phase (CLz/F)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Terminal Elimination Rate Constant (λz)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Terminal Elimination Half-Life (t1/2)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Mean Residence Time From Time Zero to Last Quantifiable Concentration (MRT0-t)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Mean Residence Time From Time Zero Extrapolated to Infinite Time (MRT0-∞)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Steady-State Trough Plasma Concentration (Cmin,ss)
大体时间:Day 7
Day 7
Steady-State Average Plasma Concentration Over One Dosing Interval (Cav,ss)
大体时间:Day 7
Day 7
Steady-State Peak-to-Trough Swing Factor (Swing)
大体时间:Day 7
Day 7
Steady-State Peak-to-Trough Degree of Fluctuation (DF)
大体时间:Day 7
Day 7
Accumulation Ratio Based on Peak Plasma Concentration (Rcmax)
大体时间:Day 1 and Day 7
Day 1 and Day 7
Accumulation Ratio Based on Area Under Curve Over One Dosing Interval (RAUC)
大体时间:Day 1 and Day 7
Day 1 and Day 7

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。

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 (估计的)

2026年8月25日

初级完成 (估计的)

2026年12月31日

研究完成 (估计的)

2026年12月31日

研究注册日期

首次提交

2026年8月13日

首先提交符合 QC 标准的

2026年8月20日

首次发布 (实际的)

2026年8月25日

研究记录更新

最后更新发布 (实际的)

2026年8月25日

上次提交的符合 QC 标准的更新

2026年8月20日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • WP107-101

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅