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Relovair PD PK in Chinese Healthy Subjects

2017年7月24日 更新者:GlaxoSmithKline

A Randomized, Double-blind, Placebo-controlled, Four-way Crossover Study to Evaluate and Compare the Pharmacodynamics and Pharmacokinetics of Fluticasone Furoate /Vilanterol in Different Dose Combination (50/25mcg, 100/25mcg and 200/25mcg) After Single and Repeat Dose Administration From a Novel Dry Powder Device in Healthy Chinese Subjects

In this study, fluticasone furoate (FF) and vilanterol (VI) in different dose combinations (50/25mcg, 100/25mcg and 200/25mcg) will be administered from a single dry powder device to evaluate the PD, PK, safety and tolerability of the combination in healthy Chinese subjects. The information gathered will be used as a support of the clinical development program of the fixed dose combination of FF/VI inhalation powder in Chinese population.

研究概览

详细说明

This is a single centre, double-blind, placebo-controlled, four-way cross over, randomized, single and repeat dose study. A total of 16 healthy subjects aged 18-45 years will be randomised with the aim of achieving at least 10 evaluable subjects to each treatment period. The primary objective is to evaluate the systemic steroid PD effects (serum cortisol 24 hour weighted mean on Day 7) of FF and systemic ß-adrenergic PD effects (ECG maximum QTcF 0-4h and whole blood potassium 0-4h in Day 1 and Day 7) of VI; the secondary objectives are aimed to evaluate the PK, safety and tolerability of FF/VI inhalation powder after a single and repeat dose administration.

研究类型

介入性

注册 (实际的)

16

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

      • Beijing、中国、100032
        • 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 45年 (成人)

接受健康志愿者

不

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 male or female between 18 and 45 years of age inclusive.
  • 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 blood pressure values outside the normal range [systolic (90-139 mmHg) and diastolic (50-89 mmHg)] and subjects with ECG findings suggestive of a previous MI should always be excluded from enrollment.
  • 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].

Child-bearing potential and agrees to use one of the contraception methods listed in Section 8.1 for an appropriate period of time (as determined by the product label or investigator) prior to the start of dosing to sufficiently minimize the risk of pregnancy at that point. Female subjects must agree to use contraception until completion of the follow-up visit.

  • 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 completion of the follow-up visit.
  • Body weight >= 50 kg and BMI within the range 19 - 24 kg/m2 (inclusive).
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
  • No significant abnormality on 12-lead ECG at screening, including the following specific requirements:

Ventricular rate >= 45 beats per minute; PR interval <=210msec; No pathological Q waves; QRS interval to be >= 60msec and <=120msec; The waveforms must enable the QT interval to be clearly defined; QTc interval must be < 450msec (QTcF; machine or manual reading) based on a single ECG value, or an average from three ECGs obtained over a brief recording period.

  • Subjects who are current non-smokers, who have not used any tobacco products in the 12 month period preceding the screening visit, and have a pack history of <=5 pack years.
  • Subjects who are able to use the inhalation device satisfactorily.

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 or on admission to the Unit.
  • A positive urinary cotinine test at screening or on admission to the Unit.
  • A positive test for HIV antibody.
  • History of regular alcohol consumption within 6 months of the study defined as: an average weekly intake of greater than 21 units or an average daily intake of greater than 3 units (males) or defined as an average weekly intake of greater than 14 units or an average daily intake of greater than 2 units (females). One unit is equivalent to a 285mL glass of full strength beer or 425mL schooner of light beer or 1 (30mL) measure of spirits or 1 glass (100mL) of wine (NHMRC Guidelines [NHMRC, 2001]).
  • 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) or 5 half-lives (whichever is longer) 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 (magnesium stearate and lactose etc.) or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.
  • History of milk protein allergy.
  • History of any adverse reaction including immediate or delayed hypersensitivity to any ICS, β2-agonist or sympathomimetic drug.
  • Blood donation or sampled as a study subject within three months preceding the first dose of study drug and blood donation during the entire study.
  • Pregnant females as determined by positive urine pregnancy test at screening or prior to dosing.
  • Lactating females.
  • Subjects who have suffered an upper or lower respiratory tract infection within 4 weeks of the screening visit.
  • The subject has taken oral corticosteroids less than 8 weeks before the screening visit.
  • The subject has taken inhaled, intranasal or topical steroids less than 4 weeks before the screening visit.
  • Unwillingness or inability to follow the procedures outlined in the protocol.
  • Subject is mentally or legally incapacitated.

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
安慰剂比较:安慰剂
匹配安慰剂
Placebo inhaled once daily for 7 days in each treatment period.
实验性的:FF/VI
50/25 mcg, 100/25 mcg or 200/25 mcg
50/25 or 100/25 or 200/25 mcg inhaled once daily for 7 days in each treatment period.

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
Systemic steroid PD effects
大体时间:Day 7
Serum cortisol
Day 7
Systemic ß-adrenergic PD effects
大体时间:Day 1 and Day 7
Maximum QTcF 0-4h and whole blood potassium
Day 1 and Day 7

次要结果测量

结果测量
措施说明
大体时间
Plasma concentrations and derived PK parameters for FF/VI
大体时间:Pre-dose, 5 min, 15 min, 30 min, 1h, 1.5h, 2h, 4h post dose on Day 1 and pre-dose, 5 min, 15 min, 30 min, 1h, 1.5h, 2h, 4h, 6h, 8h, 12h and 24h post dose on Day 7 and 8.
Single dose: Cmax, tmax, t1/2, AUC(0-t) (AUC from zero to the last quantifiable timepoint) and AUC(0-t') (AUC from zero to the last common quantifiable timepoint in the dose group). Repeat dose: FF: Cmax, tmax, t1/2, AUC(0-t) and AUC(0-t'), Ro and RCmax, Css_min and AUCss , Css_av, DF; VI: Cmax, tmax, t1/2, AUC(0-t) and AUC(0-t')
Pre-dose, 5 min, 15 min, 30 min, 1h, 1.5h, 2h, 4h post dose on Day 1 and pre-dose, 5 min, 15 min, 30 min, 1h, 1.5h, 2h, 4h, 6h, 8h, 12h and 24h post dose on Day 7 and 8.
Vital signs
大体时间:Screening Visit, Day 1, Day 7 and Follow-up Visit
blood pressure and heart rate
Screening Visit, Day 1, Day 7 and Follow-up Visit
12-lead ECG
大体时间:Screening Visit, Day 1, Day 7 and Follow-up Visit
12-lead ECG
Screening Visit, Day 1, Day 7 and Follow-up Visit
Laboratory tests
大体时间:Screening Visit, Day 8 of treatment period 4 or early withdrawal Visit and/or follow-up Visit
Clinical chemistry, hematology and urinalysis
Screening Visit, Day 8 of treatment period 4 or early withdrawal Visit and/or follow-up Visit
Adverse events
大体时间:From the start of dosing with investigational product and until the follow-up visit.
adverse events
From the start of dosing with investigational product and until the follow-up visit.

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2012年12月5日

初级完成 (实际的)

2013年6月4日

研究完成 (实际的)

2013年6月4日

研究注册日期

首次提交

2012年8月30日

首先提交符合 QC 标准的

2012年10月18日

首次发布 (估计)

2012年10月22日

研究记录更新

最后更新发布 (实际的)

2017年7月25日

上次提交的符合 QC 标准的更新

2017年7月24日

最后验证

2017年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

研究数据/文件

  1. 研究协议
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  2. 个人参与者数据集
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  3. 数据集规范
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  4. 带注释的病例报告表
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  5. 知情同意书
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  6. 临床研究报告
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register
  7. 统计分析计划
    信息标识符:115199
    信息评论:For additional information about this study please refer to the GSK Clinical Study Register

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.

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