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Completed

NCT Number: NCT00814957

An Open Label Positron Emission Tomography (PET) Study of GSK618334 in Healthy Male Subjects Using 11C-PHNO as PET Ligand

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.

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Key information

Age range

30 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

GSK Investigational Site

Harrow, Middlesex, HA1 3UJ, United Kingdom

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

GSK618334

Drug

D3 receptor antagonist

Primary outcomes

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

    Time frame: up to 48 hours

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

    Time frame: up to 48 hours

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

    Time frame: up to 48 hours

Secondary outcomes

  1. 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.

    Time frame: screening to follow-up

  2. Measuring GSK618334 in the body (pharmacokinetic endpoints): PK parameters of GSK618334 Cmax, AUCinf, tmax.

    Time frame: up to 48 hours

Sponsors and collaborators

Lead sponsor

GlaxoSmithKline

Industry

Registry information

Official study title

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.

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Dec 25, 2008
Registry last updated
Jul 7, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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