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Study to Compare Bioavailability of GLPG1972 Given as 2 Different Tablet Formulations Versus an Oral Solution

2017年6月19日 更新者:Galapagos NV

Open-label Study to Compare the Bioavailability of an Oral Wet Granulation Tablet of GLPG1972 Relative to an Oral Solution and to an Oral Direct Compression Tablet After Single-dose Intake in Healthy Subjects, and to Evaluate the Effect of Food on the Bioavailability of an Oral Wet Granulation Tablet.

This study is a Phase I, randomized, open-label, cross-over study with 4 single-dose treatments of GLPG1972 to compare the bioavailability of the oral wet granulation (WG) tablet relative to an oral solution and to the oral direct compression (DC) tablet after single dose intake in healthy male subjects and to evaluate the effect of food on the bioavailability of the WG oral tablet.

研究概览

地位

完全的

条件

干预/治疗

研究类型

介入性

注册 (实际的)

12

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

      • Antwerp、比利时
        • SGS Belgium Life Sciences

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

男性

描述

Inclusion Criteria:

  1. Male between 18 and 50 years of age, inclusive,
  2. A body mass index (BMI) between 18-30 kg/m², inclusive, weight of at least 50 kg.
  3. Judged by the investigator to be in good health based upon the results of a medical history, physical examination, vital signs, 12-lead ECG, and laboratory findings.
  4. Discontinuation of all medications except occasional paracetamol at least 2 weeks or 5 half-lives prior to the first study drug administration.
  5. Non-smokers and not using any nicotine-containing products.
  6. Negative urine drug screen and alcohol breath test.
  7. Current sexually active male agrees to use adequate contraception
  8. Willing to consume a non-vegetarian high-fat and high-calorie breakfast
  9. Able and willing to sign the ICF

Exclusion Criteria:

  1. Known hypersensitivity to study drug ingredients or a significant allergic reaction to any drug
  2. Positive serology for hepatitis B virus surface antigen (HBsAg) or hepatitis C virus (HCV) or any history of hepatitis from any cause with the exception of hepatitis A.
  3. History of or a current immunosuppressive condition
  4. Symptoms of clinically significant illness in the 3 months before the initial study drug administration.
  5. History of malignancy within the past 5 years
  6. Clinically relevant abnormalities detected on ECG regarding either rhythm or conduction (e.g. QTcF >450 msec, or a known long QT syndrome).
  7. Presence of abnormal liver function
  8. Renal function with an estimated creatinine clearance <80 ml/min based on the Cockcroft-Gault formula.
  9. Presence of any condition known to interfere with absorption, distribution, metabolism or excretion of drugs.
  10. Clinically relevant abnormalities detected on "vital signs"
  11. Dietary requirements precluding participation.
  12. Significant blood loss including blood donation or had a transfusion of any blood product within 12 weeks
  13. Hemoglobin level <7.5 mmol/L (12 g/dL).
  14. Active drug or alcohol abuse within 2 years prior to the initial study drug administration.
  15. Current (2 weeks before screening) and planned uninterrupted consumption of large quantities (> 6 cups) of coffee
  16. Administration of an injectable drug within 30 days prior to the initial study drug administration.
  17. Concurrent participation, or participation in a drug/device study within 8 weeks or 5 half-lives of the drug or within 6 months for biologicals
  18. Investigator or any sub-investigator, research assistant, pharmacist, study coordinator, or other staff

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Treatment A
GLPG1972 oral solution after overnight fast
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
实验性的:Treatment B
GLPG1972 oral DC tablet after breakfast
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
实验性的:Treatment C
GLPG1972 oral WG tablet after overnight fast
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
实验性的:Treatment D
GLPG1972 oral WG tablet after breakfast
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)

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
Assessment of the maximum observed plasma concentration of GLPG1972 after single oral doses
大体时间:on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
Determine bioavailability of GLPG1972 by assessing PK parameters
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
Assessment of plasma concentration of GLPG1972 24hrs post-dose after single oral doses
大体时间:At 24 hours post dose
Determine bioavailability of GLPG1972 by assessing PK parameters
At 24 hours post dose
Assessment of time to achieve the maximal plasma concentration of GLPG1972 after single oral doses
大体时间:on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
Determine bioavailability of GLPG1972 by assessing PK parameters
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
Assessment of the last quantifiable plasma concentration of GLPG1972 after single oral doses
大体时间:on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
Determine bioavailability of GLPG1972 by assessing PK parameters
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses

次要结果测量

结果测量
措施说明
大体时间
the number of subjects with adverse events
大体时间:at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
To assess safety and tolerability of GLPG1972 given orally
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
the number of subjects with abnormal vital signs
大体时间:at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
To assess safety and tolerability of GLPG1972 given orally
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
the number of subjects with abnormal ECG
大体时间:at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
To assess safety and tolerability of GLPG1972 given orally
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
the number of subjects with abnormal laboratory assessments
大体时间:at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
To assess safety and tolerability of GLPG1972 given orally
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours

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。

赞助

调查人员

  • 研究主任:Ann Fieuw, MD MSc、Galapagos NV

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)

2017年4月14日

初级完成 (实际的)

2017年6月6日

研究完成 (实际的)

2017年6月6日

研究注册日期

首次提交

2017年5月4日

首先提交符合 QC 标准的

2017年5月4日

首次发布 (实际的)

2017年5月8日

研究记录更新

最后更新发布 (实际的)

2017年6月20日

上次提交的符合 QC 标准的更新

2017年6月19日

最后验证

2017年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • GLPG1972-CL-105

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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GLPG1972的临床试验

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