A Study to Demonstrate Bioequivalence Between a 12-mg Dose of an Oral Suspension Formulation of Perampanel and a 12-mg Tablet Formulation of Perampanel Under Fasted and Fed Conditions in Healthy Subjects
A Randomized, Open-Label, Crossover Study to Demonstrate Bioequivalence Between a 12-mg Dose of an Oral Suspension Formulation of Perampanel and a 12-mg Tablet Formulation of Perampanel Under Fasted and Fed Conditions in Healthy Subjects
研究概览
研究类型
注册 (实际的)
阶段
- 阶段1
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria
- Healthy males or females, ages 18 to 55 years, inclusive, at the time of informed consent.
- Body mass index (BMI) of 18 to 32 kg/m2, inclusive at Screening.
- Females must not be lactating or pregnant at Screening or Baseline.
- Females of childbearing potential must not have had unprotected sexual intercourse within 30 days before study entry and must agree to use a highly effective method of contraception (eg, total abstinence, a doublebarrier method [such as condom plus diaphragm with spermicide], have a vasectomized partner with confirmed azoospermia, or an intrauterine device, contraceptive implant, or oral contraceptive that does not contain levogesterol) throughout the entire study period and for 30 days after study drug discontinuation. Females using hormonal contraceptives containing levogesterol must be on another form of contraception (such as double barrier method.) as well. If currently abstinent, the subject must agree to use a doublebarrier method as described above if she becomes sexually active during the study period or for 30 days after study drug discontinuation. Females who are using hormonal contraceptives must have been on a stable dose of the same hormonal contraceptive product for at least 4 weeks before dosing and must continue to use the same contraceptive during the study and for 30 days after study drug discontinuation. All females will be considered to be of childbearing potential unless they are postmenopausal (amenorrheic for at least 12 consecutive months, in the appropriate age group, and without other known or suspected cause) or have been sterilized surgically (i.e. bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy, all with surgery at least 1 month before dosing).
Exclusion Criteria
- Clinically significant illness that requires medical treatment within 8 weeks or a clinically significant infection that requires medical attention within 4 weeks of dosing.
- Evidence of disease that may influence the outcome of the study within 4 weeks of dosing, eg, psychiatric disorders and disorders of the gastrointestinal tract, liver, kidney, respiratory system, endocrine system, hematological system, neurological system, cardiovascular system, or subjects who have a congenital abnormality in metabolism.
- Any history of gastrointestinal surgery that may affect PK profiles of perampanel, eg, hepatectomy, nephrotomy, cholecystectomy, digestive organ resection or any gastrointestinal procedure for the purpose of weight loss (including Lapband), which would slow gastric emptying.
- Any clinically abnormal symptom or organ impairment found by medical history at Screening, and physical examinations, vital signs, electrocardiogram (ECG) finding, or laboratory test results that require medical treatment at Screening or Baseline.
- Any laboratory abnormalities considered clinically significant by the investigator.
- A prolonged QT/QTc interval (QTc greater than 450 msec) as demonstrated upon repeat ECG at Screening or Baseline.
- History of prolonged QT/QTc interval.
- History of risk factors for torsade de pointes (eg, heart failure, hypokalemia, family history of long QT syndrome).
- History of ischemic heart disease (eg, acute coronary syndromes, stable angina), syncope or cardiac arrhythmias.
- Siting heart rate less than 40 or greater than 100 beats/min at Screening or Baseline Period 1 and sitting systolic blood pressure greater than 140 mmHg or less than 90 mmHg or diastolic blood pressure greater than 90 mmHg or less than 60 mmHg at Screening or Baseline.
- Hemoglobin less than 11.5 g/dLfor females and less than 12.5 g/dL for males at screen and Baseline check-in Period 1.
- Subjects who experienced a weight loss or gain of greater than 10% between Screening and before dosing.
- Subjects who received blood products within 4 weeks, donated blood within 8 weeks, or donated plasma within 1 week of dosing.
- Hypersensitivity to the study drug or any of its excipients.
- Known history of food allergies or presently experiencing significant seasonal or perennial allergy at Screening.
- Known to be human immunodeficiency virus (HIV) positive at Screening.
- Active viral hepatitis (B or C) as demonstrated by positive serology at Screening.
- History of use of illegal (or legalized) recreational drugs in the past year.
- History of drug or alcohol dependency or abuse within approximately the last 2 years or who have a positive urine drug test or breath alcohol test at Screening or Baseline.
- Engagement in strenuous exercise within 2 weeks before dosing (eg, marathon runners, weight lifters).
- Currently enrolled in another clinical trial or used any investigational drug or device within 30 days preceding informed consent.
学习计划
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:交叉作业
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Perampanel - Group 1
Treatment A: Single oral dose of a 12-mg perampanel tablet under fasted condition. Treatment B: Single 12 mg dose of perampanel oral suspension under fasted condition. Subjects will be randomized on Study Day 1 for Treatment Period 1 to Treatment A or Treatment B. On Study Day 43 the subject will then receive the alternate Treatment for Treatment Period 2. |
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实验性的:Perampanel - Group 2
Treatment C: Single oral dose of a 12-mg perampanel tablet co-administered with high fat meal. Treatment D: Single 12 mg dose of perampanel oral suspension co-administered with high fat meal. Subjects will be randomized on Study Day 1 for Treatment Period 1 to Treatment C or Treatment D. On Study Day 43 the subject will then receive the alternate Treatment for Treatment Period 2. |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Pharmacokinetics of Perampanel: AUC(0-t)
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
|
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Pharmacokinetics of Perampanel: AUC(0-inf)
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
|
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Pharmacokinetics of Perampanel: Cmax
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Pharmacokinetics of Perampanel: AUC(0-72h)
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
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Pharmacokinetics of Perampanel: tmax
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
|
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Pharmacokinetics of Perampanel: tlag
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
|
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Pharmacokinetics of Perampanel: Lambda-z
大体时间:Up to 504 hours postdose in each treatment period
|
Up to 504 hours postdose in each treatment period
|
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Pharmacokinetics of Perampanel: t1/2
大体时间:Up to 504 hours postdose in each treatment period
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Up to 504 hours postdose in each treatment period
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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