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BA Study of IMP4297 (20mg vs 10mg) in Healthy Male Subjects

2021年8月21日 更新者:Impact Therapeutics, Inc.

An Open-Label, Randomized, Single-Dose, 2-Way Crossover Study to Compare the Bioavailability of Two IMP4297 Formulations (20 mg Capsules and 10 mg Capsules) After Single Oral Administration of 100 mg IMP4297 Under Fasted Condition in Healthy Male Subjects

An open-label, randomized, single-dose, 2-way crossover study to compare the bioavailability of two IMP4297 formulations (20 mg capsules and 10 mg capsules) after single oral administration of 100 mg IMP4297 under fasted condition in healthy male subjects

研究概览

地位

完全的

条件

干预/治疗

详细说明

This will be an open-label, randomized, single-dose, 2-way crossover study to compare the bioavailability of two IMP4297 formulations (10 mg capsules and 20 mg capsules) after single oral administration of 100 mg IMP4297 under fasted condition in healthy male subjects. It will be conducted at one site, and approximately a total of 18 subjects will be enrolled.

Subjects will be randomized to one of the 2 treatment sequences according to a computer-generated randomization schedule. Each treatment sequence will consist of 2 periods, separated by a washout period of at least 7 days between each period.

研究类型

介入性

注册 (实际的)

18

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。

学习地点

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 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

男性

描述

Inclusion Criteria:

  1. Healthy male subjects, 18 to 55 years of age (both inclusive) on the day of signing informed consent form (ICF).
  2. Body Mass Index (BMI) of 18 to 30 kg/m2 (both inclusive); and a total body weight 50 kg.
  3. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, physical examination, including blood pressure (BP), pulse rate (PR) measurement, temperature, 12-lead ECG, or clinical laboratory tests, etc., judged by the investigator. For example, the reference normal ranges (inclusive) are as follows: after at least 5-minute rest in a supine position, BP: 90-139/60-89 mmHg, and PR: 50-100 bpm. Repeat assessment can be conducted at the discretion of the investigator or delegate.
  4. Subjects able to father children must use a highly effective non-drug contraception double barrier method for the duration of the study and for at least 90 days after the last dose of study medication and should not have any plan for sperm donation throughout this period. Note: Sexual abstinence is allowed if this is the preferred and usual lifestyle of the subject. Male subjects are also eligible to participate if they have a bilateral vasectomy or have a female partner of non-childbearing potential.
  5. Subjects must voluntarily participate in this study. Be willing and be able to provide written informed consent for this clinical trial. Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
  6. Subjects who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion Criteria:

  1. Evidence or history of clinically significant diseases, including but not limited to neurologic, cardiovascular, hematological, immunological, renal, hepatic, gastrointestinal, pulmonary, endocrine, metabolic, psychiatric, or allergic disease (including drug and food allergies).
  2. Any condition possibly affecting drug absorption (e.g., gastrectomy, difficulty in swallowing).
  3. General anesthesia within 3 months before administration, or have a planned surgery during the study period.
  4. History of drug abuse within the past 5 years, or a positive urine drug test at screening or the admission. Repeat assessment can be conducted at the discretion of the investigator or delegate.
  5. History of excessive alcohol intake exceeding 10 drinks/week (1 standard drink = 150 mL of wine, 360 mL of beer, or 45 mL of hard liquor) within 3 months prior to screening, or a positive alcohol breath test at screening or the admission. Repeat assessment can be conducted at the discretion of the investigator or delegate.
  6. Use of tobacco or nicotine containing products in excess of the equivalent of 5 cigarettes per day within 3 months prior to screening, a positive urine nicotine test at screening or the admission, or difficulty abstaining from smoking for the duration of study confinement. Repeat assessment can be conducted at the discretion of the investigator or delegate.
  7. Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to the first dose of study drug; participation in a clinical trial of device(s) within 30 days prior to the first dose of study drug; participation in ≥4 clinical trials within one year prior to the first dose of study drug.
  8. Blood donation (excluding plasma donations) or significant loss of blood (≥400 mL) within 1 month prior to screening, received blood transfusion or use of blood products.
  9. Use of any medicinal product that changes the activity of hepatic enzymes within 28 days prior to the first dose of study drug, such as potent CYP3A4 inhibitors or inducers, or subjects who need to continue receiving these medications during the study period (refer to Appendix 18.2 for the list of common CYP3A4 inhibitors or inducers).
  10. Use of prescription or nonprescription drugs, dietary supplements, or herbal medicines, within 14 days or 5 half-lives (whichever is longer) prior to the first dose of study drug. As an exception, paracetamol may be used at doses of ≤1 g/day. Limited use of nonprescription medications that are not believed to affect the overall results of the study may be permitted on a case by case basis following approval by the principal investigator and the sponsor.
  11. Subjects with history of hepatitis, or positive result at screening for hepatitis B surface antigen (HepBsAg), hepatitis B core antibody (HepBcAb), hepatitis C antibody (HCVAb), or human immunodeficiency virus antibody (HIVAb).
  12. Screening supine 12-lead ECG demonstrating a QTcF (using Fridericia's formula, QTcF = QT/RR1/3) interval >450 msec, or a QRS interval >120 msec. If QTcF >450 msec or QRS >120 msec, the ECG should be repeated 2 more times and the average of the 3 QTcF or QRS values should be used to determine the subject's eligibility.
  13. Unable to abstain from strenuous exercise within 48 hours prior to dosing and during the study period.
  14. Use of products containing alcohol, tobacco, nicotine, caffeine within 48 hours prior to dosing; or unable to abstain from using these products for the duration of study confinement.
  15. History of sensitivity to any ingredients of IMP4297 products evaluated in this study.
  16. History of hemophobia, inability to tolerate venipuncture, and being afraid of needles.
  17. Subjects who have received live vaccine within 28 days prior to screening.
  18. Any other medical or psychiatric condition that may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for study participation.

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:其他
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Arm 1

Period 1:

100 mg oral dose of IMP4297 (5 capsules, 20 mg/capsule);

Period 2:

100 mg oral dose of IMP4297 (10 capsules, 10 mg/capsule);

Each treatment sequence will consist of 2 periods, separated by a washout period of at least 7 days between each Dose.

IMP4297 10mg/capsule; IMP4297 20mg/capsule;
实验性的:Arm 2

Period 1:

100 mg oral dose of IMP4297 (10 capsules, 10 mg/capsule);

Period 2:

100 mg oral dose of IMP4297 (5 capsules, 20 mg/capsule);

Each treatment sequence will consist of 2 periods, separated by a washout period of at least 7 days between each Dose.

IMP4297 10mg/capsule; IMP4297 20mg/capsule;

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
Cmax
大体时间:3 months
peak concentration
3 months
AUC0-last
大体时间:3 months
area under the curve from time zero to the time with the last quantifiable concentration
3 months
AUC0-inf
大体时间:3 months
area under the curve from time zero to infinity
3 months

次要结果测量

结果测量
措施说明
大体时间
Safety endpoints
大体时间:3 months
Number of participants with treatment-related adverse events as assessed by CTCAE v4.03
3 months
Tmax
大体时间:3 months
time to reach Cmax
3 months
t½
大体时间:3 months
elimination half-life
3 months
CL/F
大体时间:3 months
apparent clearance
3 months
Vz/F
大体时间:3 months
apparent volume of distribution
3 months

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 (实际的)

2020年10月29日

初级完成 (实际的)

2021年2月11日

研究完成 (实际的)

2021年4月30日

研究注册日期

首次提交

2020年4月15日

首先提交符合 QC 标准的

2020年4月16日

首次发布 (实际的)

2020年4月17日

研究记录更新

最后更新发布 (实际的)

2021年8月24日

上次提交的符合 QC 标准的更新

2021年8月21日

最后验证

2021年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • IMP4297-107

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

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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