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A Single Oral Escalating Dose Study of GSK2140944 in Healthy Volunteers

2017年6月9日 更新者:GlaxoSmithKline

A Randomized, Single Blind, Placebo Controlled Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single Escalating Oral Doses of GSK2140944 in Healthy Adult Subjects

GSK2140944 belongs to the Bacterial Type II Topoisomerase Inhibitor (BTI) class of antibiotics. GSK2140944 has demonstrated in vitro and in vivo activity against Gram positive including methicillin resistant Staphylococcus aureus (MRSA) and Gram-negative pathogens associated with respiratory tract, skin and soft tissue infections including isolates resistant to existing classes of antimicrobials. This is a First Time in Human (FTIH) study to assess the safety, tolerability, and pharmacokinetics of single oral doses of GSK2140944 in healthy volunteers. This study will be a single-blind, randomized, placebo-controlled, dose-rising study in healthy subjects. The proposed single doses will range from 100 mg to 3000 mg.

研究概览

详细说明

GSK2140944 belongs to the Bacterial Type II Topoisomerase Inhibitor (BTI) class of antibiotics which is being developed for treatment of Gram positive [including methicillin resistant Staphylococcus aureus (MRSA)] and Gram-negative pathogens associated with respiratory tract and skin and soft tissue infections including isolates resistant to existing classes of antimicrobials.

Study BTZ114595 will be the first administration of GSK2140944 in humans. This study will examine the safety, tolerability, and pharmacokinetics of escalating single oral doses of GSK2140944. The predicted clinical target for efficacy, based on preclinical efficacy models, is an AUC(0-24) of 16-30 μg.h/mL. This study aims to explore the safety and tolerability at and above target exposures in order to establish a therapeutic window for this compound.

This study will investigate the safety, tolerability, and pharmacokinetics of escalating single oral doses of GSK2140944.

This will be a randomized, placebo-controlled, single-blind study to determine safety, tolerability, and single dose pharmacokinetic (PK) profile of GSK2140944 in healthy subjects.

The projected single escalating doses of GSK2140944 will range from a starting dose of 100 mg to a maximum dose of 3000 mg. The current plan is to administer the study drug after an overnight fast, but based on emerging PK and safety data, it may be necessary to administer the study drug under fed state to better understand safety, tolerability or PK of GSK2140944. Any decision to remove or modify fasting requirements will be made by the GSK Study Team and the investigator based on joint review of the emerging safety, tolerability and preliminary pharmacokinetic data from prior dose-levels.

研究类型

介入性

注册 (实际的)

48

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

    • Minnesota
      • Minneapolis、Minnesota、美国、55404
        • GSK Investigational Site

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 60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:

  • AST, ALT, alkaline phosphatase and bilirubin ≤ 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%)
  • 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.
  • Male or female ranging from 18 to 60 years of age, at the time of signing the informed consent. Female subject must be 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]. Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods in Section 8.1 if they wish to continue their HRT during the study. Otherwise, they must discontinue HRT to allow confirmation of post-menopausal status prior to study enrollment. For most forms of HRT, at least 2-4 weeks will elapse between the cessation of therapy and the blood draw; this interval depends on the type and dosage of HRT. Following confirmation of their post-menopausal status, they can resume use of HRT during the study without use of a contraceptive method.
  • Body weight ≥ 50 kg and BMI within the range 19 - 31 kg/m2, inclusive.
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
  • QTcF < 450 msec, or QTc < 480 msec in subjects with Bundle Branch Block., at screening.

Exclusion Criteria:

  • Any clinically significant central nervous system (e.g., seizures), cardiac, pulmonary, metabolic, renal, hepatic or gastrointestinal conditions or history of such conditions that, in the opinion of the investigator may place the subject at an unacceptable risk as a participant in this trial or may interfere with the absorption, distribution, metabolism or excretion of drugs.
  • A positive urine test for drugs of abuse or alcohol (or alcohol breath test) at screening.
  • A screening urinalysis positive for protein or glucose (greater than "trace" findings of protein or glucose).
  • Positive for Human Immunodeficiency Virus (HIV) antibody, hepatitis B virus surface antigen, or hepatitis C virus antibody at screening.
  • History of drug abuse within 6 months of the study.
  • History of smoking or use of nicotine containing products within 3 months of screening, or a positive urine cotinine indicative of smoking at screening.
  • History of regular alcohol consumption exceeding an average weekly intake of greater than or equal to 21 units for men/14 units for women or an average daily intake of greater than or equal to 3 units for men/2 units for women. One unit is equivalent to a 285 mL glass of full strength beer or 425 mL schooner of light beer or 1 (30 mL) measure of spirits or 1 glass (100 mL) of wine.
  • The subject has participated in a clinical trial and has received a drug or a new chemical entity within 30 days or 5 half-lives, or twice the duration of the biological effect of any drug (whichever is longer) prior to the first dose of current study medication.
  • Use of prescription or non-prescription drugs, including vitamins above the recommended daily intake (National Health and Medical Research Council in Australia guideline), herbal and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study medication, or use of St. John's Wort within 14 days prior to the first dose of study medication. By exception, the volunteer may take paracetamol or acetaminophen (≤ 2 grams/day) or ibuprofen (1600 mg/day) up to 48 hours prior to the first dose of study medication. However, the investigator and study team can review medication use on a case by case basis to determine if its use would compromise subject safety or interfere with study procedures or data interpretation.
  • Consumption of red wine, seville oranges, grapefruit or grapefruit juice, pummelos, exotic citrus fruits or grapefruit hybrids or fruit juices containing such products for 7 days prior to administration of study medication.
  • Donation of blood in excess of 550 mL within 12 weeks prior to dosing.
  • An unwillingness of male subjects to abstain from sexual intercourse with pregnant or lactating women, or an unwillingness of male subjects to use a condom and spermicide, in addition to having their female partner use another form of contraception such as an IUD, diaphragm with spermicide, oral contraceptives, injectable progesterone, subdermal implants or a tubal ligation, if engaging in sexual intercourse with a female partner who could become pregnant. This criterion must be followed from the time of study medication administration and until 84 days after study medication administration.
  • 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 physician responsible, contraindicates their participation.
  • History of sensitivity to heparin or heparin-induced thrombocytopenia (if the clinical research unit uses heparin to maintain intravenous cannula patency).
  • An unwillingness to comply with lifestyle and/or dietary restrictions as described in Section 8.

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:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:Matching Placebo
Placebo
安慰剂
实验性的:GSK2140944
Dose range 100mg to 3000mg single dose
Investigational Study Drug

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
按不良事件 (AE) 数量评估的 GSK2140944 临床安全数据
大体时间:直至后续访问
在整个研究过程中,安全性和耐受性参数将包括 AE 的记录
直至后续访问
GSK2140944 clinical safety data assessed as change from baseline in 12-lead ECG
大体时间:Day 1, Day 2, Day 3 and at the Follow-up visit
12-lead ECGs will be obtained at each timepoint using an ECG machine, after the subject has rested in the supine position for at least 10 minutes
Day 1, Day 2, Day 3 and at the Follow-up visit
GSK2140944 clinical safety data from dual-lead cardiac monitoring
大体时间:Day -1, Day 1
Continuous dual-lead cardiac monitoring will be obtained at each timepoints using an ECG machine
Day -1, Day 1
GSK2140944 clinical safety data assessed as change from baseline in clinical laboratory tests
大体时间:Day -1, Day 2, Day 3 and the Follow-up visit
Clinical laboratory assessments will include hematology, clinical chemistry, routine urinalysis and additional parameters
Day -1, Day 2, Day 3 and the Follow-up visit
GSK2140944 clinical safety data assessed as change from baseline in blood pressure
大体时间:Day -1, Day 1, Day 2, Day 3 and the Follow-up visit
Vital sign measurements will include systolic and diastolic blood pressure
Day -1, Day 1, Day 2, Day 3 and the Follow-up visit
GSK2140944 clinical safety data assessed as change from baseline in heart rate
大体时间:Day -1, Day 1, Day 2, Day 3 and the Follow-up visit
Vital sign measurements will include pulse rate
Day -1, Day 1, Day 2, Day 3 and the Follow-up visit

次要结果测量

结果测量
措施说明
大体时间
Pharmacokinetic parameter: AUC(0-t) following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC(0-t)) following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: AUC(0-infinity) following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC(0-infinity)) following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: Cmax following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include maximum observed concentration (Cmax) following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: tmax following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include time of occurrence of Cmax (tmax) following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: t1/2 following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include terminal phase half-life (t1/2) following single dose of GSK2140944
Up to Day 4
To assess preliminary dose proportionality using PK parameter AUC(0-infinity) following single dose of GSK2140944
大体时间:Up to Day 4
Preliminary dose proportionality will be assessed using PK parameter (AUC(0-infinity)) following single dose of GSK2140944
Up to Day 4
To assess preliminary dose proportionality using PK parameter Cmax following single dose of GSK2140944
大体时间:Up to Day 4
Preliminary dose proportionality will be assessed using PK parameter Cmax following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: (Ae) following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include urinary recovery of unchanged drug (Ae) following single dose of GSK2140944
Up to Day 4
Pharmacokinetic parameter: (CLr) following single dose of GSK2140944
大体时间:Up to Day 4
Pharmacokinetic data will include renal clearance (CLr) following single dose of GSK2140944
Up to Day 4

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)

2011年9月26日

初级完成 (实际的)

2012年2月15日

研究完成 (实际的)

2012年2月15日

研究注册日期

首次提交

2012年3月29日

首先提交符合 QC 标准的

2014年7月24日

首次发布 (估计)

2014年7月28日

研究记录更新

最后更新发布 (实际的)

2017年6月12日

上次提交的符合 QC 标准的更新

2017年6月9日

最后验证

2017年6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

  • 114595

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