此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

LEO 32731 - A Study in Healthy Male Subjects

2013年11月4日 更新者:LEO Pharma

LEO 32731 - A Phase I, Single-Blind, Placebo Controlled, Single and Multiple Oral Dose, Safety, Tolerability and Pharmacokinetic Study in Healthy Subjects

The purpose of this first-in-man trial is to determine the safety and tolerability of ascending single and multiple doses of LEO 32731 in healthy male subjects. The trial will be performed in three parts. In Part 1, single doses of LEO 32731 will be administered to healthy male subjects. In Part 2, the effect of food on the single oral dose pharmacokinetic will be investigated. In Part 3, multiple doses of LEO 32731 will be administered to healthy male subjects.

研究概览

地位

完全的

干预/治疗

研究类型

介入性

注册 (实际的)

111

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

      • Leeds、英国
        • Covance Clinical Research Unit Ltd.

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 55年 (成人)

接受健康志愿者

有资格学习的性别

男性

描述

Inclusion Criteria:

  1. Subjects will, prior to any study related activities, have given their written informed consent to participate in the study and to abide by the study restrictions.
  2. Subjects will be Caucasian males between 18 and 55 years of age and with a body mass index (BMI) between 18.0 and 30.0 kg/m2 inclusive.
  3. Subjects must be in good health, as determined by a medical history, physical examination, 12-lead electrocardiogram (ECG) and clinical laboratory evaluations (congenital non haemolytic hyperbilirubinaemia is NOT acceptable).

Exclusion Criteria:

  1. Subjects who are not, or whose partners are not willing to use appropriate contraception (such as condom) with spermicidal foam/gel/film/cream/suppository from the time of the first dose until 3 months after the final dosing occasion. Male subjects whose partners are of child-bearing potential must also agree to use an additional highly effective method of contraception
  2. Subjects who have received any prescribed systemic or topical medication within 14 days of the first dose administration unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.
  3. Subjects who have used any non-prescribed systemic or topical medication (including herbal remedies) within 7 days of the first dose administration unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.
  4. Subjects who have received any medications, including St John's Wort, known to chronically alter drug absorption or elimination processes within 30 days of the first dose administration unless in the opinion of the Investigator the medication will not interfere with the study procedures or compromise safety.
  5. Subjects who are still participating in a clinical study (e.g. attending follow-up visits) or who have participated in a clinical study involving administration of an investigational drug (new chemical entity), or a marketed drug within the past 3 months prior to the first dosing occasion.
  6. Subjects who have donated any blood, plasma or platelets in 3 months prior to screening or who have made donations on more than two occasions within the 12 months preceding the first dose administration.
  7. Subjects with a significant history of drug allergy as determined by the Investigator.
  8. Subjects who have any clinically significant allergic disease (excluding non-active hayfever) as determined by the Investigator.
  9. Subjects who have a supine blood pressure and supine pulse rate at screening higher than 140/90 mmHg and 100 beats per minute (bpm), respectively, or lower than 90/50 mmHg and 50 bpm, respectively
  10. Subjects who consume more than 28 units of alcohol per week or who have a significant history of alcoholism or drug/chemical abuse as determined by the Investigator (one unit of alcohol equals ½ pint [285 mL] of beer or lager, one glass [125 mL] of wine, or 1/6 gill [25 mL] of spirits).
  11. Subjects with a positive urine drug screen or alcohol breath test result at screening or first admission.
  12. Subjects who smoke or who have smoked in the 3 months prior to first dose administration.
  13. Subjects with, or with a history of, any clinically significant neurological, gastrointestinal, renal, hepatic, cardiovascular, psychiatric, respiratory, metabolic, endocrine, haematological, dermatological or other major disorders as determined by the Investigator.
  14. Subjects who have had a clinically significant illness within 4 weeks of the start of dose administration as determined by the Investigator.
  15. Subjects who are known to have serum hepatitis, or who are carriers of the hepatitis B surface antigen (HBsAg) or hepatitis C antibody, or who have a positive result to the test for HIV antibodies.
  16. Subjects who have confirmed active/latent tuberculosis (TB).
  17. Subjects who, in the opinion of their General Practitioner (GP) or the Investigator, should not participate in the study, including subjects suspected for whatever reason of not being able to comply with the requirements of the protocol.
  18. Subjects who have an abnormality in the 12-lead ECG that, in the opinion of the investigator, increases the risk of participating in the study; such as QTcB interval >450 msec, 2nd or 3rd degree Atrioventricular block, complete left bundle branch block, complete right bundle branch block or Wolff-Parkinson-White Syndrome defined as PR<110 msec, confirmed by a repeat ECG.
  19. Subjects who have previously taken part in or withdrawn from this study.
  20. Subjects who, in the opinion of the Investigator, should not participate in the study.

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

  • 分配:随机化
  • 介入模型:单组作业
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:LP0058 oral solution (0.050 mg/mL)
LEO 32731
  • Part 1 and 2: Oral single dose of oral solution or capsule
  • Part 3: Twice daily dose of oral solution or capsule for 7 days
实验性的:LP0058 oral solution (0.200 mg/mL)
LEO 32731
  • Part 1 and 2: Oral single dose of oral solution or capsule
  • Part 3: Twice daily dose of oral solution or capsule for 7 days
安慰剂比较:LP0058 oral solution (placebo)
Placebo
  • Part 1 and 2: Oral single dose of oral solution or capsule
  • Part 3: Twice daily dose of oral solution or capsule for 7 days
实验性的:LP0058 capsule 1-120 mg
LEO 32731
  • Part 1 and 2: Oral single dose of oral solution or capsule
  • Part 3: Twice daily dose of oral solution or capsule for 7 days
安慰剂比较:LP0058 capsule (placebo)
Placebo
  • Part 1 and 2: Oral single dose of oral solution or capsule
  • Part 3: Twice daily dose of oral solution or capsule for 7 days

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of subjects with AEs and change from baseline in vital signs (blood pressure, pulse rate and oral body temperature), ECG, telemetry and clinical laboratory.
大体时间:7 days after last dosing
7 days after last dosing

次要结果测量

结果测量
大体时间
LEO 32731 and metabolites in blood and urine
大体时间:72 hours after dosing
72 hours after dosing

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

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

2011年3月1日

初级完成 (实际的)

2012年8月1日

研究完成 (实际的)

2012年11月1日

研究注册日期

首次提交

2011年3月2日

首先提交符合 QC 标准的

2011年3月4日

首次发布 (估计)

2011年3月7日

研究记录更新

最后更新发布 (估计)

2013年11月5日

上次提交的符合 QC 标准的更新

2013年11月4日

最后验证

2011年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • LP0058-S01

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.

LEO 32731的临床试验

3
订阅