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Emotional Processing in Healthy Volunteers in the Presence of an Investigational Anxiolytic

Primary Purpose

Depressive Disorder and Anxiety Disorders

Status
Completed
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Citalopram
GSK424887
Plactebo To Match
Sponsored by
GlaxoSmithKline
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder and Anxiety Disorders focused on measuring healthy volunteers, Anxiety Disorder, neuropsychological tests

Eligibility Criteria

18 Years - 45 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Healthy males with no neurological, or history of psychiatric illness
  2. Aged between 18 and 45 years
  3. Agree to use contraception
  4. BMI range of 18 to 33 kg/m²
  5. Fluent English speakers
  6. Non smoker or light smoker

Exclusion Criteria:

  1. Positive pre-study drug/alcohol screen or regular alcohol consumption
  2. Positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
  3. On prescription or non prescription drug
  4. Exposure to more than four new chemical entities within 12 months prior to the first dosing day
  5. Consumption of large amounts of caffeinated drinks
  6. Significant hearing impairment
  7. Previous experience of the emotional test battery experimental procedures

Sites / Locations

  • GSK Investigational Site

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Placebo Comparator

Arm Label

Citalopram

Investigational Medicinal Product

Placebo To Match Treatment

Arm Description

Marketed comparitor

GSK424887

Placebo control

Outcomes

Primary Outcome Measures

Multiple emotional and psychometric battery of tests
Adverse Events, laboratory values, vital signs, ECGs

Secondary Outcome Measures

Full Information

First Posted
February 12, 2010
Last Updated
July 5, 2017
Sponsor
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT01424384
Brief Title
Emotional Processing in Healthy Volunteers in the Presence of an Investigational Anxiolytic
Official Title
Emotional Processing in Healthy Male Volunteers Treated With GSK424887. A Single Centre, Randomised, Double-blind, Placebo-controlled Parallel Group Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
September 19, 2008 (Actual)
Primary Completion Date
April 30, 2009 (Actual)
Study Completion Date
April 30, 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GlaxoSmithKline

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This will be a phase I, single centre, randomised, double blind, double-dummy, placebo controlled, parallel group single-dose study in healthy volunteers. The purpose of this study is to assess the effect of a single-dose administration of GSK424887, a potent, selective competitive antagonist of the human Neurokinin 1 (NK1) receptor and a potent inhibitor of the human serotonin transporter (SERT), at the maximum dosage of 100 mg versus placebo and versus citalopram (20 mg) on emotional processing in healthy male volunteers. Pharmacokinetics and safety following oral administration of GSK424887 will be also evaluated. An Emotional Test Battery (ETB) previously used to characterise the effects of antidepressants on positive and negative emotion processing in Healthy Volunteers and patients will be used. We hypothesise that GSK424887 will modulate emotional information processing acutely. We anticipate that these effects may be manifest at sub-effective levels of NK1 and SERT receptor occupancy, thus providing pharmacodynamic evidence of the synergistic interaction of the two mechanisms in humans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder and Anxiety Disorders
Keywords
healthy volunteers, Anxiety Disorder, neuropsychological tests

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Citalopram
Arm Type
Active Comparator
Arm Description
Marketed comparitor
Arm Title
Investigational Medicinal Product
Arm Type
Experimental
Arm Description
GSK424887
Arm Title
Placebo To Match Treatment
Arm Type
Placebo Comparator
Arm Description
Placebo control
Intervention Type
Drug
Intervention Name(s)
Citalopram
Intervention Description
Neurophysiological testing.
Intervention Type
Drug
Intervention Name(s)
GSK424887
Intervention Description
Neurophysiological testing
Intervention Type
Drug
Intervention Name(s)
Plactebo To Match
Intervention Description
Neurophysiological testing
Primary Outcome Measure Information:
Title
Multiple emotional and psychometric battery of tests
Time Frame
< 1 day
Title
Adverse Events, laboratory values, vital signs, ECGs
Time Frame
< 1 day

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy males with no neurological, or history of psychiatric illness Aged between 18 and 45 years Agree to use contraception BMI range of 18 to 33 kg/m² Fluent English speakers Non smoker or light smoker Exclusion Criteria: Positive pre-study drug/alcohol screen or regular alcohol consumption Positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening On prescription or non prescription drug Exposure to more than four new chemical entities within 12 months prior to the first dosing day Consumption of large amounts of caffeinated drinks Significant hearing impairment Previous experience of the emotional test battery experimental procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GSK Clinical Trials
Organizational Affiliation
GlaxoSmithKline
Official's Role
Study Director
Facility Information:
Facility Name
GSK Investigational Site
City
Oxford
ZIP/Postal Code
OX3 7JX
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.
Citations:
PubMed Identifier
23407644
Citation
Harmer CJ, Dawson GR, Dourish CT, Favaron E, Parsons E, Fiore M, Zucchetto M, Bifone A, Poggesi I, Fernandes S, Alexander RC, Goodwin GM. Combined NK(1) antagonism and serotonin reuptake inhibition: effects on emotional processing in humans. J Psychopharmacol. 2013 May;27(5):435-43. doi: 10.1177/0269881112472558. Epub 2013 Feb 12.
Results Reference
background
Links:
URL
https://www.clinicalstudydatarequest.com
Description
Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Informed Consent Form
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Annotated Case Report Form
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Statistical Analysis Plan
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Clinical Study Report
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Dataset Specification
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register
Available IPD/Information Type
Individual Participant Data Set
Available IPD/Information URL
https://www.clinicalstudydatarequest.com
Available IPD/Information Identifier
105012
Available IPD/Information Comments
For additional information about this study please refer to the GSK Clinical Study Register

Learn more about this trial

Emotional Processing in Healthy Volunteers in the Presence of an Investigational Anxiolytic

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