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Dose Tolerance Study in Healthy Male Volunteers After Intranasal Application of Epinastine Nasal

2014年10月7日 更新者:Boehringer Ingelheim

A Double-blind, Randomised, Placebo-controlled Single Increasing Dose Tolerance Study in Healthy Male Volunteers After Intranasal Application of Epinastine Nasal (Dosage: 0.035 mg (0.025 % Solution) - 0.42 mg (0.3 % Solution))

Safety, tolerability and pharmacokinetics

研究概览

地位

完全的

条件

研究类型

介入性

注册 (实际的)

39

阶段

  • 阶段1

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

21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:

  • All participants in the study should be healthy, range from 21 to 50 years of age and be within ± 20 % of their normal weight (Broca -Index)
  • Subsequently each subject will have his medical history taken and will receive a complete medical examination (incl. blood pressure and pulse rate measurements) as well as a 12-lead ECG. Haematological, hepatic and renal function tests will be carried out in the laboratory (Bioscientia Ingelheim, Germany). The subjects will fast for 12 hours before collection of specimens for all laboratory evaluations. The above mentioned examinations will be performed within 14 days before the first administration of the test substance
  • In accordance with good clinical practice (GCP) and the local legislation all volunteers will have given their written informed consent prior to admission to the study

Exclusion Criteria:

  • Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • Surgery of the gastro-intestinal tract (except appendectomy)
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  • History of orthostatic hypotension, fainting spells or blackouts
  • Chronic or relevant acute infections
  • History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
  • Intake of drugs with a long half-life (> 24 hours) within at least one month or less than ten half-lives of the respective drug before enrolment in the study
  • Use of any drugs which might influence the results of the trial (≤ one week prior to administration or during the trial)
  • Participation in another trial with an investigational drug (≤ two months prior to administration or during the trial
  • Smoker (> 10 cigarettes or > 3 cigars or > 3 pipes/day)
  • Inability to refrain from smoking on trial days
  • Alcohol abuse (> 60 g/day)
  • Drug abuse
  • Blood donation (≥ 100 mL within four weeks prior to administration or during the trial)
  • Excessive physical activities (within the last week before the study)
  • Any laboratory value outside the reference range of clinical relevance

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:安慰剂
实验性的:Epinastine nasal
single rising doses

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
Number of patients with clinically relevant findings in vital signs
大体时间:up to 8 days after drug administration
blood pressure, pulse rate
up to 8 days after drug administration
Number of patients with clinically relevant findings in 12-lead ECG
大体时间:up to 8 days after drug administration
up to 8 days after drug administration
Number of patients with adverse events
大体时间:up to 8 days after drug administration
up to 8 days after drug administration
Number of patients with clinically relevant findings in laboratory parameters
大体时间:up to 8 days after drug administration
up to 8 days after drug administration
Changes in rhinoscopy assessment
大体时间:up to 8 days after drug administration
up to 8 days after drug administration

次要结果测量

结果测量
措施说明
大体时间
Maximum measured concentration in plasma (Cmax)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Time from dosing to the maximum concentration in plasma (tmax)
大体时间:up to 48 hours drug administration
up to 48 hours drug administration
Area under the concentration-time curve in plasma (AUC)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Terminal rate constant of in plasma (λz)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Apparent terminal half-life in plasma (t1/2)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Total mean residence time in the body (MRTtot)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Total clearance in plasma after extravascular administration (CL/F)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Apparent volume of distribution during the terminal phase (Vz/F)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Amount excreted into urine (Ae)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Renal clearance (CLR)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Assessment of dose-proportionality of epinastine nasal
大体时间:up to 48 hours after drug administration
based on AUC and Cmax
up to 48 hours after drug administration

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。

有用的网址

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

2001年8月1日

初级完成 (实际的)

2001年9月1日

研究注册日期

首次提交

2014年10月7日

首先提交符合 QC 标准的

2014年10月7日

首次发布 (估计)

2014年10月9日

研究记录更新

最后更新发布 (估计)

2014年10月9日

上次提交的符合 QC 标准的更新

2014年10月7日

最后验证

2014年10月1日

更多信息

与本研究相关的术语

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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