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Brain Uptake of GSK1034702: a Positron Emission Tomography (PET) Scan Study

An Open Label Positron Emission Tomography (PET) Study to Investigate Brain Penetration by [Carbonyl-11C] GSK1034702 in Healthy Subjects

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00937846
Enrollment
4
Registered
2009-07-13
Start date
2009-07-15
Completion date
2009-08-28
Last updated
2017-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Disorders

Keywords

Cognitive impairment, Schizophrenia, Alzheimer's Disease, PET

Brief summary

GSK1034702 is being developed for improving cognitive impairment in diseases such as Alzheimer's disease and schizophrenia. This study will be done in healthy men to investigate how much of the study drug gets into the brain. This will be done using Positron Emission Tomography (PET).

Detailed description

This is an open label, single dose, non-randomized PET study in healthy male subjects to ascertain if GSK1034702 is crossing the blood-brain barrier to enable it to elicit a central effect. GSK1034702 has been shown in vitro to be a substrate for human Pgp, therefore the distribution of GSK1034702 into human brain could be adversely affected. This use of PET in conjunction with radioactively labelled GSK1034702 will help ascertain the role Pgp plays in limiting brain penetration in the presence and absence of a pharmacological relevant oral non labelled dose of 5 mg. Subjects will have an MRI scan to aid definition of brain anatomy, a baseline PET scan and a post-dose PET scan. For each subject the study will consist of at least three visits; screening visit, scanning day and follow-up.

Interventions

Single oral 5 mg dose in liquid formulation

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
35 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Generally healthy. * Male between 35 and 55 years of age. * Willing to use appropriate contraception method. * Weight more than 50 kg. * BMI within the range 19 - 29 kg/m2. * Adequate blood supply to the hand.

Exclusion criteria

* Abuse of drugs or alcohol. * Smoker or history of regular use of tobacco- or nicotine-containing products in the past 6 months. * ECG abnormality (personal or family history). * Psychiatric disorder. * Asthma or a history of asthma. * Medical illness. * Worked as a welder, metal worker or machinist. * Suffers from claustrophobia or would be unable to lie still in a PET or MRI scanner for 1-2 hours. * Has a cardiac pacemaker or other electrical device or ferromagnetic metal foreign bodies. * Neurological disorder

Design outcomes

Primary

MeasureTime frame
Volume of distribution of [11C]GSK1034702 at tracer and pharmacological doses.Scanning day

Secondary

MeasureTime frame
The kinetic rate constants at tracer and pharmacological doses.Scanning day
GSK1034702 PK parameters: Cmax; tmax; AUC(0-t).Scanning day
Safety and tolerability endpoints consisting of: AEs; 12-lead ECG; 12 lead digital Holter and lead II telemetry; vital signs; clinical laboratory evaluations.2 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026