Evaluation of Dose-Dependent Repeated-Dose Neramexane Effects on Cardiac Repolarisation (QT/QTc Interval Duration): Electrocardiogram (ECG) Study in Healthy Adult Subjects
2011年2月14日 更新者:Merz Pharmaceuticals GmbH
Valuation of Dose-Dependent Repeated-Dose Neramexane Effects on Cardiac Repolarisation (QT/QTc Interval Duration) Randomized, Double-Blind, Placebo- and Moxifloxacin-Controlled, Ascending Repeated-Dose, Three-Arm Parallel Design ECG Study in Healthy Adult Subjects
Primary:
- To assess the effects of ascending repeated-doses of oral [p.o.] neramexane at therapeutic and supra-therapeutic steady-state doses on cardiac repolarisation (QT/QTc interval) in healthy male and female subjects.
Secondary:
- To assess the pharmacokinetics [PK] of neramexane and N-OH neramexane (if a validated method will be available for this metabolite) following repeated daily doses of 50 mg (steady state), 75 mg (steady state) and 87.5 mg (steady state).
- To assess the safety and tolerability of neramexane 50 mg, 62.5 mg, 75 mg and 87.5 mg repeated-dose treatments when gradually up-titrated in healthy subjects.
- To assess the concentration-QT relationship.
研究概览
研究类型
介入性
注册 (预期的)
126
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
-
-
-
Berlin、德国、14050
- Parexel International GmbH
-
-
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
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Healthy adult subject confirmed on the basis of extensive pre-study screening investigations
- Aged 18 to 45, inclusive
- Body mass index [BMI] of 18-28 kg/m² (inclusive) and a body weight of 50 -<90 kg
- Willing and able to provide written informed consent after having been informed of the requirements and the restrictions of the study
- Female subject of child-bearing potential must agree to use a non-hormonal highly effective method of birth control defined as those which result in a low failure rate when used consistently and correctly, such as sexual abstinence, vasectomized partner, non-hormone releasing intrauterine devices [IUDs].
A sexually active man, who has not been sterilized surgically, must agree to use together with his female partner a double contraception method during intercourse:
- IUD or hormonal contraception plus condom or diaphragm or spermicide, or
- condom plus diaphragm or observe abstinence during the entire clinical study until the Final Examination.
Exclusion Criteria:
- History of clinically relevant allergy or known hypersensitivity to neramexane/memantine/amantadine and their derivatives
- History of clinically relevant allergy or known hypersensitivity to moxifloxacin or any other quinolone antibiotics
- History of clinically relevant allergy or known hypersensitivity to any inactive ingredient in any of the used investigational products or positive control especially quinine
- Any contraindications which are indicated in the current SPC of Avalox®
- Evidence or (family) history of long QT syndrome
- Exposure to another investigational agent within the last two months before Day -1
- Lactating or pregnant female, or female planning to become pregnant during study conduct
- Any evidence of a significant cardiovascular, pulmonary, renal, hepatic, gastrointestinal, endocrinological, metabolic (acidosis), psychiatric, neurologic, relevant eye disorder or other diseases at screening
- ECG abnormalities of clinical relevance, in particular abnormal prolongations of QT/QTc-interval (i.e. QTc >450 ms, PQ ≥220 ms)
- Systolic blood pressure <95 mmHg or >140 mmHg or diastolic blood pressure <50 mmHg or >95 mmHg in semi-supine position
- Pulse rate <45 or >100 beats per minute
- History of malignancy
- Any clinically relevant deviation in clinical or laboratory assessment
- Acute or chronic clinically relevant infections
- Current evidence of hypokalemia and/or hypomagnesemia (= below lower limit of laboratory normal range plus 0.3 mmol/L as safety margin)
- History of alcohol or illicit drug abuse
- Alcohol consumption averaging more than 40 g for male and more than 20 g for female subjects daily within the last year
- Alcohol consumption within the last 48 hours prior to Day -1 or illicit drug intake in the 4 weeks prior to Day -1
- Disorders or surgery of the gastrointestinal tract which may interfere with drug absorption or may otherwise influence the pharmacokinetics of the investigational medicinal products (e.g. cholecystectomy, resections of small or large intestine, febrile conditions, chronic diarrhea, chronic vomiting, endocrine disease severe infections, acute inflammations, etc.)
- Allergy to band aid
- Use of any prescribed drugs in the 4 weeks prior to Day -1
- Regular use of over-the-counter [OTC] drugs (except paracetamol, maximum 1 g/day) in the 4 weeks prior to Day -1
- Occasional use of OTC drugs (except paracetamol, maximum 1 g/day) in the 2 weeks prior to Day -1
- Use of any food, food supplement or medication known to induce or inhibit cytochrome P450 [CYP] 2B6 or any other clinical relevant CYP enzymes within two weeks preceding Day -1 (e.g. grapefruit, St. Johns wort)
- Regular caffeine consumption averaging more than 1 L of coffee and/or tea daily or more than 1 L of caffeine-containing lemonades per day within the last year
- Female subject who employed any form of hormonal contraception within 2 months prior to study Day -1 (e.g. oral contraceptives, hormone releasing IUDs, etc.)
- Consume of xanthine derivates (including coffee, tea, chocolate, etc.) or quinine containing beverages (Bitter Lemon, Tonic Water, etc.) within two days prior to Day -1
- Smoker
- Previous participation in the drug administration phase of this trial
- Blood donation more than 450 mL within 60 days prior to Day -2
- Positive results in any of the serology tests (Human Immunodeficiency Virus [HIV1/2] antibodies, hepatitis B surface antigen, antibodies against hepatitis C virus)
- Positive pregnancy test
- Positive drug screen or alcohol test
- Excessive sports within 3 days before Day -2
- Sauna within 48 hours before Day -2
- Employee or direct relative of an employee of the CRO or Merz Pharmaceuticals
- Evidence or suspicion that the subject might not comply with the study directives and/or that he/she is not reliable or trustworthy
- Evidence or suspicion that the subject is not willing or unable to understand the information that is given to him/her as part of the informed consent, in particular regarding the risks and discomfort to which he/she would agree to be exposed
- Vulnerable subject (e.g. person kept in detention)
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
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Neramexane, Placebo, Moxifloxacin
|
Dosage form: 25 mg immediate release [IR] tablets (=15.9 mg neramexane free base) 37.5 mg IR tablets (=23.9 mg neramexane free base) |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
To assess the effects of ascending repeated-doses of oral [p.o.] neramexane at therapeutic and supra-therapeutic steady-state doses on cardiac repolarisation (QT/QTc interval) in healthy male and female subjects.
大体时间:steady state, therapeutic dose
|
steady state, therapeutic dose
|
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
2009年9月1日
初级完成 (实际的)
2010年4月1日
研究完成 (实际的)
2010年4月1日
研究注册日期
首次提交
2009年9月10日
首先提交符合 QC 标准的
2009年9月16日
首次发布 (估计)
2009年9月17日
研究记录更新
最后更新发布 (估计)
2011年2月15日
上次提交的符合 QC 标准的更新
2011年2月14日
最后验证
2011年2月1日
更多信息
与本研究相关的术语
其他研究编号
- MRZ 92579/TI/1006
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.