Single Dose Escalation Study of GSK2838232 in Healthy Subjects
2017年5月5日 更新者:GlaxoSmithKline
A Double-Blind, Randomized, Placebo-Controlled, Single Dose Escalation First Time in Human Study to Investigate the Safety, Tolerability and Pharmacokinetics of GSK2838232 and to Evaluate the Effect of Food and Ritonavir on GSK2838232 in Healthy Subjects
GSK2838232 is a novel human immune virus (HIV) maturation inhibitor being developed for the treatment of chronic HIV infection.
This study is the first administration of GSK2838232 in humans to establish the initial safety, tolerability, and pharmacokinetic profile following single doses of GSK2838232 and to evaluate the effect of food and ritonavir (RTV) on GSK2838232 in healthy subjects.
There will be 2 cohorts in this study.
In Cohort 1, approximately 8 healthy subjects will be enrolled (6 active and 2 placebo) at each dose visit.
There will be four dosing sessions for each subject with subjects randomized to receive placebo in a random sequence.
In Cohort 2, approximately 8 healthy subjects will be enrolled (6 active doses and 2 placebo doses at each dose visit).
Cohort 2 will have four dosing sessions for each subject with subjects randomized to receive placebo in a random sequence.
研究概览
研究类型
介入性
注册 (实际的)
17
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
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Maryland
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Baltimore、Maryland、美国、21225
- GSK Investigational Site
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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 50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
- Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. A subject with a clinically significant abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator and the GSK Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures
- Male or female between 18 and 50 years of age inclusive, at the time of signing the informed consent. A female subject is eligible to participate if she is of non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea (in questionable cases a blood sample with simultaneous follicle stimulating hormone >40 milli international unit [MlU]/milliliter [mL] and estradiol <40 picogram [pg]/mL [<147 picomoles /liter] is confirmatory).
- Body weight >= 50 kilograms (kg) (110 pounds.) for men and >= 45 kg (99 pounds) for women and body mass index (BMI) within the range 18.5 to 31.0 kg/meter^2 (inclusive).
- A Creatinine clearance (CLcr) >80 mL/minute (min) as determined by Cockcroft-Gault equation. CLcr (mL/min) = (140 - age) x weight / (72 x serum creatinine [Scr]) (times 0.85 if female) where age is in years, weight is in kg, and Scr is in units of milligram (mg)/deciliter (dL).
- Male subjects with female partners of child-bearing potential must agree to use contraception method. This criterion must be followed from the time of the first dose of study medication until the follow up visit.
- Subject must be capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Exclusion Criteria
- A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.
- Alanine aminotransferase (ALT), alkaline phosphatase and bilirubin >= 1.5x Upper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent).
- Screening or baseline cardiac troponin I greater than the 99 percent cutoff (>.045 nanogram [ng]/mL by the Dimension Vista cardiac troponin I [CTNI] assay).
- Screening BNP greater than the upper limit of normal
- Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
- A positive pre-study drug/alcohol screen.
- A positive test for Human Immuno Virus antibody.
- History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >14 drinks for males or >7 drinks for females. One drink is equivalent to 12 grams of alcohol: 12 ounces (360 mL) of beer, 5 ounces (150 mL) of wine or 1.5 ounces (45 mL) of 80 proof distilled spirits.
- The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
- Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
- Unable to refrain from the use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GlaxoSmithKline (GSK) Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
- History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
- Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
- Pregnant females as determined by positive urine or serum human chorionic gonadotropin (hCG) test at screening or prior to dosing on Day 1.
- Lactating females.
- History of sensitivity to heparin or heparin-induced thrombocytopenia.
- Subjects who have asthma or a history of asthma
- A history of or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.
- Unable to refrain from consumption of red wine, seville oranges, grapefruit or grapefruit juice and/or pummelos, exotic citrus fruits, grapefruit hybrids or fruit juices from 7 days prior to the first dose of study medication.
- Subjects with a pre-existing condition interfering with normal gastrointestinal anatomy or motility, hepatic and/or renal function, that could interfere with the absorption, metabolism, and/or excretion of the study drugs. Subjects with a history of cholecystectomy should be excluded.
- Exclusion Criteria for 24-Hour Screening Holter are: any symptomatic arrhythmia (except isolated extra systoles), sustained cardiac arrhythmias (such as atrial fibrillation or flutter, supraventricular tachycardia (>=10 consecutive beats), complete heart block), non-sustained or sustained ventricular tachycardia (defined as >= 3 consecutive ventricular ectopic beats), any conduction abnormality (including but not specific to left or right incomplete or complete bundle branch block, atrioventricular (AV) block [2nd degree or higher], Wolff-Parkinson-White [WPW]syndrome etc.), sinus Pauses > 3 seconds, 300 or more supraventricular ectopic beats in 24 hours, and 250 or more ventricular ectopic beats in 24 hours.
- Exclusion criteria for screening ECG (a single repeat is allowed for eligibility determination) are: Male subjects with Heart rate <45 and >100 beats per minute (bpm) and female subjects with heart rate <50 and >100 bpm, PR <120 and >220 milliseconds (msec), QRS duration <70 and >120 msec, QT interval corrected for heart rate (Fridericia's) >450 msec. (Note: A heart rate from 100 to 110 bpm can be rechecked by ECG or vitals within 30 minutes to verify eligibility).
Evidence of previous myocardial infarction (Does not include ST segment changes associated with repolarization).
Any conduction abnormality (including but not specific to left or right complete bundle branch block, AV block [2nd degree or higher], WPW syndrome).
Sinus Pauses > 3 seconds. Any significant arrhythmia which, in the opinion of the principal investigator OR GSK medical monitor, will interfere with the safety for the individual subject.
Non-sustained or sustained ventricular tachycardia (>=3 consecutive ventricular ectopic beats).
- Medical history of cardiac arrhythmias or cardiac disease or a family and personal history of long QT syndrome.
- Any clinically significant abnormal echocardiogram finding. Abnormal echocardiogram findings should be discussed with the Medical Monitor prior to enrolment.
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:交叉作业
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Cohort 1
Subject in this cohort will be randomized to one of the four following treatment sequences (1 treatment per visit): ABCD, BACD, BCAD, or BCDA.
Where A=Placebo, B= GSK2838232 5mg, C=GSK2838232 10mg, and D=GSK2838232 20mg
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Bottled powder with 5, 10 and 20mg unit dose strength per single dose for re-constituted oral suspension given once daily
Visually matching GSK2838232
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实验性的:Cohort 2
Subject in this cohort will be randomized to one of the four following treatment sequences (1 treatment per visit): EGHJ, FEHJ, FGIJ, or FGHK.
Where E=Placebo, F= GSK2838232 50mg, G= GSK2838232 100mg, H= GSK2838232 50mg + food, I= Placebo + food, J= GSK2838232 10mg + RTV, K= placebo + RTV.
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Bottled powder with 5, 10 and 20mg unit dose strength per single dose for re-constituted oral suspension given once daily
Visually matching GSK2838232
100mg tablets once daily for 12 days
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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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Number of subjects with adverse events (AEs) as a measure of safety and tolerability in cohort 1
大体时间:Up to 16 weeks
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AEs will be collected from the start of Study Treatment and until 5 days post last-dose (at follow up).
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Up to 16 weeks
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Number of subjects with AEs as a measure of safety and tolerability in cohort 2.
大体时间:Up to 12 weeks
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AEs will be collected from the start of Study Treatment and until 5 days post last-dose (at follow up).
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Up to 12 weeks
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Absolute values and changes over time of hematology as a measure of safety and tolerability in cohort 1.
大体时间:Up to 16 weeks
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Up to 16 weeks
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Absolute values and changes over time of hematology as a measure of safety and tolerability in cohort 2
大体时间:Up to 12 weeks
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Up to 12 weeks
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Absolute values and changes over time of clinical chemistry as a measure of safety and tolerability in cohort 1.
大体时间:Up to 16 weeks
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Up to 16 weeks
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Absolute values and changes over time of clinical chemistry as a measure of safety and tolerability in cohort 2.
大体时间:Up to 12 weeks
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Up to 12 weeks
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Absolute values and changes over time of urinalysis as a measure of safety and tolerability in cohort 1.
大体时间:Up to 16 weeks
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Up to 16 weeks
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Absolute values and changes over time of urinalysis as a measure of safety and tolerability in cohort 2
大体时间:Up to 12 weeks
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Up to 12 weeks
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Absolute values and changes over time of vital signs as a measure of safety and tolerability in cohort 1
大体时间:Up to 16 weeks.
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Vital signs include blood pressure, temperature and heart rate measurement
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Up to 16 weeks.
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Absolute values and changes over time of vital signs as a measure of safety and tolerability in cohort 2.
大体时间:Up to 12 weeks
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Vital signs include blood pressure, temperature and heart rate measurement
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Up to 12 weeks
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Absolute values and changes over time of ECG intervals and ECG rhythm as a measure of safety and tolerability in cohort 1.
大体时间:Up to 16 weeks.
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Up to 16 weeks.
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Absolute values and changes over time of ECG intervals and ECG rhythm as a measure of safety and tolerability in cohort 2.
大体时间:Up to 12 weeks
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Up to 12 weeks
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Real time collection and review of heart rhythm using telemetry as a measure of safety and tolerability in cohort 1.
大体时间:Up to 16 weeks.
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Up to 16 weeks.
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Real time collection and review of heart rhythm using telemetry as a measure of safety and tolerability in cohort 2.
大体时间:Up to 12 weeks
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Up to 12 weeks
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Composite of pharmacokinetics (PK) parameters following single dose administration of GSK2838232 in cohort 1
大体时间:PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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PK parameters include: area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC [0-infinity]), area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC [0-t]), maximum observed concentration (Cmax), time to maximum observed concentration (Tmax), observed concentration at 24hour post-dose (C24), last observed quantifiable concentration (Ct), lag time before observation of drug concentrations in sampled matrix (tlag), terminal half-life (t1/2), and apparent oral clearance (CL/F).
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PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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Composite of pharmacokinetics parameters following single dose administration of GSK2838232 in cohort 2.
大体时间:PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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PK parameters include: AUC (0-infinity), AUC (0-t), Cmax, Tmax, C24, Ct, tlag, t1/2 and CL/F.
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PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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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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Composite of pharmacokinetics parameters following single dose administration of GSK2838232 with and without food in cohort 2.
大体时间:PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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PK parameters include: AUC (0-infinity), AUC (0-t), Cmax, Tmax, C24 and t1/2.
Food will be normal fat meal.
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PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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Composite of pharmacokinetics parameters following single dose administration of GSK2838232 with co-administration of ritonavir in cohort 2.
大体时间:PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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PK parameters include: AUC (0-infinity), AUC (0-t), Cmax, Tmax, C24 and t1/2.
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PK samples will be collected at pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, and 72 hours post dose in each dosing session and at follow up visit.
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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。
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)
2013年2月18日
初级完成 (实际的)
2013年11月21日
研究完成 (实际的)
2013年11月21日
研究注册日期
首次提交
2013年2月14日
首先提交符合 QC 标准的
2013年2月28日
首次发布 (估计)
2013年3月4日
研究记录更新
最后更新发布 (实际的)
2017年5月9日
上次提交的符合 QC 标准的更新
2017年5月5日
最后验证
2017年5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
- 116787
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