A Randomized, Single Blind, Placebo Controlled Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single Oral Doses and Repeat Escalating Oral Doses of GSK2251052 in Healthy Adult Subjects
2017年6月27日 更新者:GlaxoSmithKline
GSK2251052 ((S)-3-(aminomethyl)-7-(3-hydroxypropoxy)-1-hydroxy-1,3-dihydro-2,1-benzoxaborole hydrochloride) is a Gram negative antibacterial compound currently in development for the treatment of hospital acquired Gram negative infection (including E. coli, K. pneumoniae, and Enterobacter spp.)
This study will be conducted in two (2) parts, with single oral doses being explored in Part A (500, 1000, and 2000 mg) and repeat oral doses (1000 and 2000 mg, b.i.d.) being explored in Part B. Parts A and B will be single-blind, randomized, placebo-controlled, dose-rising studies in healthy subjects to evaluate the safety, tolerability and pharmacokinetics of oral GSK2251052.
研究概览
研究类型
介入性
注册 (实际的)
84
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
-
-
South Australia
-
Adelaide、South Australia、澳大利亚、5000
- 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 65年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- AST, ALT, alkaline phosphatase and bilirubin < or = 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
- Abnormal LFT tests may be repeated once at the discretion of the Investigator. If an abnormality is repeated, the subject would not be eligible for inclusion.
- 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 clinical 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. Subjects with coagulation, reticulocyte, or Hgb values outside the normal range should always be excluded from enrollment.
- Male or female between 18 and 65 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 (FSH) > 40 MlU/ml and estradiol < 40 pg/ml (<147 pmol/L) is confirmatory].
- Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods listed in Section 8.1. This criterion must be followed from the time of the first dose of study medication until at least 90 days post-last dose.
- Body weight > 50 kg and BMI within the range 19 - 32 kg/m2 (inclusive).
- Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
- QTc, QTcB or QTcF < 450 msec; or QTc < 480 msec in subjects with Bundle Branch Block.
Exclusion Criteria:
- A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
- 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 HIV antibody.
- History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (~240 ml) of beer, 1 glass (125 ml) of wine or 1 (25 ml) measure of 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.
- 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) prior to the first dose of study medication, unless in the opinion of the Investigator and 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 serum or urine hCG test at screening or prior to dosing.
- Lactating females.
- Unwillingness or inability to follow the procedures outlined in the protocol.
- Subject is mentally or legally incapacitated.
- History of sensitivity to heparin or heparin-induced thrombocytopenia.
- Subjects who have asthma or a history of asthma, (e.g., for any FTIH where risk of bronchoconstriction is unknown, or compound specific where risk of bronchoconstriction).
- Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.
- 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.
- A history of orthostatic hypotension
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:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Part A Cohort 1
GSK2251052 500 mg (6 subjects), Placebo (1 subject)
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part A Cohort 2
GSK2251052 1000 mg (6 subjects), Placebo (1 subject)
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part A Cohort 3
GSK2251052 2000 mg (6 subjects), Placebo (1 subject)
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part A Cohort 2 - fed
GSK2251052 1000 mg (6 subjects), Placebo (1 subject)
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part B Cohort 1
Placebo (3 subjects), GSK2251052 (9 subjects) dose to be determined
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part B Cohort 2
Placebo (3 subjects), GSK2251052 (9 subjects) dose to be determined
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part B Cohort 3
Placebo (3 subjects), GSK2251052 (9 subjects) dose to be determined
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
|
实验性的:Part A Cohort 4
Placebo (1 subject), GSK2251052 (6 subjects) dose to be determined
|
匹配的安慰剂片剂
500 mg tablet, dose levels detailed in Arm description
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Adverse event reporting, clinical laboratory tests, vital signs, cardiac monitoring, urinalysis, and clinical monitoring/observation.
大体时间:within 35 days of first dose
|
within 35 days of first dose
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Plasma AUC(0-t), AUC(0-inf), Cmax, tmax, t1/2, Ae, fe, and CLr of GSK2251052 as data permit.
大体时间:within 14 days of first dose
|
within 14 days of first dose
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
AUC(0-t), AUC(0-inf), and Cmax following single dose administration for the assessment of dose proportionality
大体时间:within 72 h of dosing
|
within 72 h of dosing
|
|
Trough plasma concentrations
大体时间:within 10 days of first dose
|
within 10 days of first dose
|
|
Accumulation based on AUC(Ro) and Cmax (RCmax) and determine the steady-state ratio (Rss)
大体时间:within 14 days of first dose
|
within 14 days of first dose
|
|
AUC(0-t)am and Cmax,am following repeat administration at different doses for the assessment of dose proportionality
大体时间:within 14 days of first dose
|
within 14 days of first dose
|
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)
2010年10月7日
初级完成 (实际的)
2011年8月25日
研究完成 (实际的)
2011年8月25日
研究注册日期
首次提交
2010年12月16日
首先提交符合 QC 标准的
2010年12月16日
首次发布 (估计)
2010年12月17日
研究记录更新
最后更新发布 (实际的)
2017年6月28日
上次提交的符合 QC 标准的更新
2017年6月27日
最后验证
2017年6月1日
更多信息
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.