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临床试验/NCT00814957
NCT00814957已完成1 期

An Open Label Positron Emission Tomography Study in Healthy Male Subjects to Investigate Brain Dopamine D3 Receptor Occupancy, Pharmacokinetics and Safety of Single Oral Doses of GSK618334, Using 11C-PHNO as PET Ligand.

GlaxoSmithKline1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2008年12月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
12
试验地点
1
主要终点
Binding of PHNO, PET ligand, in each region of interest at each scan.

研究概览

简要总结

The purpose of this study is to investigate the relationship between the plasma concentrations of the study drug and the amount of the study drug bound to the D3 receptors of the brain after dosing of a new compound GSK618334.

详细描述

This imaging study will be an open label, non-randomised PET receptor occupancy study using healthy male volunteers. The time course and degree of D3 receptor occupancy (RO) after single doses of GSK618334 will be determined using 11C-PHNO as a PET ligand labeling dopamine receptor. The PK/PD relationship between plasma concentrations of GSK618334 and D3 RO will be described. Potential relationships between D3 RO and functional magnetic resonance imaging (fMRI) endpoints will be assessed as an exploratory aim.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • healthy, male subjects aged between 30 and 55 old inclusive.
  • normal body weight.
  • normal ECG and vital signs.
  • agree to use acceptable contraceptive methods required.
  • capable of giving written informed consent.

排除标准

  • smoker or uses other nicotine-containing products.
  • certain medical conditions including heart disease, neurological disease, gastrointestinal disease, kidney or liver dysfunction - abnormal laboratory tests.
  • certain psychiatric conditions and use of certain psychoactive drugs .
  • positive blood alcohol or urine drug test.
  • alcohol intake over 14 drinks per week.
  • participation in another drug trial within 30 days or a study involving significant radiation exposure.
  • donation of more than 450 mL blood within the 56 days.
  • family history of cancer (one or more first-degree relative diagnosed before the age of 55 years old).
  • having cardiac pacemaker or other electronic device.
  • suffers from claustrophobia or feels that he will be unable to lie still on his back in the PET camera.

研究组 & 干预措施

Open-label

Experimental

D3 receptor antagonist

干预措施: GSK618334 (Drug)

结局指标

主要结局

Binding of PHNO, PET ligand, in each region of interest at each scan.

时间窗: up to 48 hours

Percentage of PHNO, PET ligand, occupancy in each region of interest after a single oral dose of GSK618334 for each individual.

时间窗: up to 48 hours

Time course of GSK618334 concentration in blood following a single oral dose.

时间窗: up to 48 hours

次要结局

  • Adverse events and other safety assessments such as clinically relevant changes in electrocardiography (ECG); vital signs (blood pressure, heart rate); laboratory safety data and physical examination.(screening to follow-up)
  • Measuring GSK618334 in the body (pharmacokinetic endpoints): PK parameters of GSK618334 Cmax, AUCinf, tmax.(up to 48 hours)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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