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。

Safety, Tolerability,Pharmacokinetics and Pharmacodynamics of ODM-106 in Healthy Volunteers (FIMPAM)

2016年10月28日 更新者:Orion Corporation, Orion Pharma

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effects of Single Escalating Doses of ODM-106: A Randomised, Double-blind, Placebo-controlled Single Centre Study in Healthy Males

The study is a dose escalation study with 8 planned dose levels. The study is a 4-period crossover design where each healthy volunteer will be randomised to receive three dose levels of ODM-106 (single doses) and one dose of placebo. The study will look at the pharmacokinetics (how the body handles the drug) and pharmacodynamics (how the drug affects the body) of ODM-106.

研究概览

地位

完全的

详细说明

Eight planned dose levels of ODM-106 will be compared with placebo.There will be 2 panels of subjects with 4 dose levels in each panel. Subjects will be randomised to receive 3 dose levels of active treatment (single doses) and 1 dose of placebo. The dose levels will be escalated from the smallest dose upwards within the study and within the study subject. A third panel of 8 subjects may be included to investigate further dose levels of ODM-106, investigate the effect of taking ODM-106 with food or to compare two different formulations of ODM-106. For an individual subject, the study will consist of a screening period (maximum 4 weeks), 4 study treatment periods with a wash-out period between each study treatment administration and a post-treatment period of about 2 weeks.

The study duration for an individual will be approximately 12-16 weeks. Blood samples will be collected for the assessment of the concentration of ODM-106 and its metabolite.Plasma samples and cumulative urinary samples will be collected for metabolite screening. Safety will be assessed by a 12-lead electrocardiogram (ECG), continuous ECG monitoring, Holter ECG, supine and orthostatic blood pressure and heart rate, body temperature, physical examination, electroencephalogram (EEG), laboratory safety assessments and adverse events. Sedation and psychomotor tests and a quantitative EEG will also be performed.

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

      • Berlin、德国
        • 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

男性

描述

Inclusion Criteria:

  • Written informed consent obtained.
  • Participants must be able to speak, read and understand German.
  • Good general health ascertained by detailed medical history and physical examinations.
  • Males 18-45 years (inclusive).
  • Body mass index (BMI) 18-30 kg/m2 inclusive
  • Weight 55-95 kg (inclusive).
  • Participants with female partners of child-bearing potential must adhere to a proper form of contraception from first study treatment administration until 3 months after the end-of-study visit.

Exclusion Criteria:

  • A predictable poor compliance or inability to understand and comply with protocol requirements, instructions and protocol-stated restrictions or communicate well with the investigator.
  • Vulnerable subjects.
  • Veins unsuitable for repeated venipuncture.
  • Evidence of clinically relevant cardiovascular, renal, hepatic, haematological, gastro-intestinal, pulmonary, metabolic-endocrine, neurological, urogenital or psychiatric disease as judged by the investigator. The participants should be healthy subjects.
  • Subjects with a medical history of relevant psychiatric disorders or evidence of significant neuropsychiatric disease
  • Any condition requiring regular concomitant medication including herbal products or likely to need any concomitant medication during the study.
  • Definite or suspected personal history of hypersensitivity to drugs or excipients.
  • Intake of any medication that could affect the outcome of the study, as judged by the investigator, within 2 weeks before first study treatment administration (2 months for enzyme inducing drugs like rifampicin or carbamazepin), or less than 5 times the half-life of the medication.
  • A history of alcoholism or excess alcohol intake (including regular consumption of more than 21 units of alcohol per week) .
  • Use of nicotine-containing products within 6 months of admission and inability to refrain from using nicotine-containing products during the study.
  • History of drug abuse or positive drug screen for amphetamine, barbiturates, benzodiazepines, cannabinoids, cocaine, opiates, methamphetamine or methadone.
  • Propensity to get headache when refraining from caffeine-containing beverages.
  • Blood donation or loss of clinically relevant amount of blood within 2 months before the screening visit.
  • Abnormal 12-lead ECG finding of clinical relevance at the screening visit
  • Heart rate (HR) < 50 bpm or > 90 bpm after 10 min in rest (supine) at the screening visit
  • At the screening visit: systolic BP < 90 mmHg or > 140 mmHg, diastolic BP < 50 mmHg or > 90 mmHg, orthostatic hypotension decrease of greater than or equal to 20 mmHg for systolic BP, decrease of greater than or equal to 10 mmHg for diastolic BP.
  • Abnormal 24-h Holter of clinical relevance at the screening visit,
  • Positive serology to human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibodies.
  • Any abnormal value of laboratory, vital signs, or physical examination, which may in the opinion of the investigator interfere with the interpretation of the test results or cause a health risk for the subject if he takes part in the study.
  • Participation in an investigational drug study within 2 months before entry into this study.
  • An employee, a direct or indirect relative of the employee of the contract research organisation or the sponsor.
  • Any other condition that in the opinion of the investigator would interfere with the evaluation of the results or constitute a health risk for the subject.
  • Subject with abnormal standard EEG judged as clinically relevant by the investigator at screening.

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:基础科学
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Drug: ODM-106
Oral capsules dosage 2-800mg once daily for one day
Single oral escalating doses of ODM-106 will be administered. Each subject will participate in 4 study periods and will therefore receive 3 single doses of ODM-106 and one single dose of placebo.
安慰剂比较:Drug: Placebo
Oral capsules given once daily for one day
Single oral escalating doses of ODM-106 will be administered. Each subject will participate in 4 study periods and will therefore receive 3 single doses of ODM-106 and one single dose of placebo.

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 Participants With Adverse Events as a Measure of Safety. Number of Participants With Adverse Events Related to Tolerability.
大体时间:From screening up to 16 weeks
Clinically relevant changes from baseline in safety laboratory assessments (haematology, clinical chemistry, urinalysis), vital signs (pulse and heart rate), 12 lead electrocardiograms, Holter electrocardiograms, telemetry, physical examination.
From screening up to 16 weeks

次要结果测量

结果测量
措施说明
大体时间
Peak Plasma Concentration (cMax) of ODM-106
大体时间:Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level.
cMax of ODM-106 after single dosing of either Capsule B or Capsule A
Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level.
Area Under the Plasma Concentration Versus Time Curve (AUC) of ODM-106
大体时间:Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level. Urine sampling, pre-dose and for 24 hours post dose at each dose level
AUC of ODM-106 after single oral dosing of either Capsule B or Capsule A.
Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level. Urine sampling, pre-dose and for 24 hours post dose at each dose level
Time to Peak Plasma Concentration (Tmax) of ODM-106
大体时间:Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level
tmax of ODM-106 after single oral dosing of Capsule B or Capsule A
Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level
Elimination Half-life of ODM-106
大体时间:Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level.
Elimination half-life of ODM-106 after single dosing of either Capsule B or Capsule A
Pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level.
Metabolite Screening in Plasma and Urine
大体时间:Plasma samples at pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level. Urine samples, pre-dose and for 24 hours post dose at each dose level
Metabolite screening in plasma and urine after single dosing
Plasma samples at pre-dose and 15, 30 and 45 min, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 48, 72 and 96 hours post dose at each dose level. Urine samples, pre-dose and for 24 hours post dose at each dose level
Effect of ODM-106 on Growth Hormone Levels
大体时间:Predose and 1, 2, 3,4, 6 and 8 hours post dose at each dose level.
Growth hormone levels (Cmax) in serum after single oral dosing with either ODM-106 Capsule B, ODM-106 Capsule A or placebo.
Predose and 1, 2, 3,4, 6 and 8 hours post dose at each dose level.
Sedation Scores on a Visual Analogue Scale (VAS)
大体时间:Pre-dose and at 1, 6 and 10.5h post dose at each dose level
Assessment of sedation by subject
Pre-dose and at 1, 6 and 10.5h post dose at each dose level
Dexterity and Reaction Times
大体时间:Pre-dose and at 1 and 6h post dose at each dose level
Selected battery of psychomotor tests
Pre-dose and at 1 and 6h post dose at each dose level
Quantitative EEG
大体时间:Pre-dose and at 1, 6 and 10 h post dose at each dose level
Quantitative analysis of EEG
Pre-dose and at 1, 6 and 10 h post dose at each dose level

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。

调查人员

  • 首席研究员:Rainard Fuhr, MD、Parexel International GmbH, Berlin, Germany
  • 研究主任:John Whiteside、Orion Corporation, Orion Pharma

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

2015年3月1日

初级完成 (实际的)

2015年10月1日

研究完成 (实际的)

2016年3月1日

研究注册日期

首次提交

2015年3月6日

首先提交符合 QC 标准的

2015年3月13日

首次发布 (估计)

2015年3月20日

研究记录更新

最后更新发布 (估计)

2016年12月23日

上次提交的符合 QC 标准的更新

2016年10月28日

最后验证

2016年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • 3117001
  • 2014-001317-33 (EudraCT编号)

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.

订阅