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The Effects of OC000459 on Nasal Mediators

Primary Purpose

Allergic Rhinitis

Status
Completed
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Study drug administration
Skin prick test
12-lead ECG
Laboratory safety samples
Alcohol breath test
Smokerlyzer test
Urine drug test
Blood test for drug concentrations
Nasal allergen challenge
Nasal filter paper placement
Total nasal symptoms scores
Sponsored by
Imperial College London
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Allergic Rhinitis focused on measuring Allergic rhinitis

Eligibility Criteria

18 Years - 50 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: 1. Males aged 18 to 50 years with a history of symptoms of grass pollen related allergic rhinitis within the previous two years. Exclusion Criteria: 1. Medical conditions likely to affect the outcome of the study. 2 History of immunotherapy in the past 3 years or currently on an immunotherapy treatment course including inhaled or local corticosteroids in the past 28 days. 3. Any infirmity, disability, or geographic location which, in the opinion of the principal investigator, would limit compliance with the protocol.

Sites / Locations

  • National Heart & Lung Institute Clinical Studies Unit

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
February 10, 2006
Last Updated
May 27, 2015
Sponsor
Imperial College London
Collaborators
Oxagen Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT00290381
Brief Title
The Effects of OC000459 on Nasal Mediators
Official Title
The Effects of OC000459 on Nasal Th2 Cytokine Release, Eosinophil Responses, and Nasal Symptoms After Nasal Allergen Challenge (NAC) With Timothy Grass Pollen in Subjects With Allergic Rhinitis Out of Season
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Imperial College London
Collaborators
Oxagen Ltd

4. Oversight

5. Study Description

Brief Summary
This is the first proof of concept study for OC000459 and is undertaken to assess the effects of the compound on the development of inflammatory cytokines in a model (nasal allergen challenge model) that is validated and clinically safe and easy to conduct. OC000459 will be compared with placebo in the study. The study will be a randomised, double blind, placebo controlled, crossover evaluation of the effect of OC000459 on cytokine secretion induced by nasal allergen challenge. Male subjects with a known history of allergic rhinitis and screening positive to allergen will be included. After dosing with OC000459 or placebo, nasal allergen challenge will be performed and measurements made in the nasal fluids. Nasal symptom scores will also be recorded. Safety parameters will be monitored throughout.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis
Keywords
Allergic rhinitis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
20 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Study drug administration
Intervention Type
Procedure
Intervention Name(s)
Skin prick test
Intervention Type
Procedure
Intervention Name(s)
12-lead ECG
Intervention Type
Procedure
Intervention Name(s)
Laboratory safety samples
Intervention Type
Procedure
Intervention Name(s)
Alcohol breath test
Intervention Type
Procedure
Intervention Name(s)
Smokerlyzer test
Intervention Type
Procedure
Intervention Name(s)
Urine drug test
Intervention Type
Procedure
Intervention Name(s)
Blood test for drug concentrations
Intervention Type
Procedure
Intervention Name(s)
Nasal allergen challenge
Intervention Type
Procedure
Intervention Name(s)
Nasal filter paper placement
Intervention Type
Procedure
Intervention Name(s)
Total nasal symptoms scores

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 1. Males aged 18 to 50 years with a history of symptoms of grass pollen related allergic rhinitis within the previous two years. Exclusion Criteria: 1. Medical conditions likely to affect the outcome of the study. 2 History of immunotherapy in the past 3 years or currently on an immunotherapy treatment course including inhaled or local corticosteroids in the past 28 days. 3. Any infirmity, disability, or geographic location which, in the opinion of the principal investigator, would limit compliance with the protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Trevor T Hansel, FRCPath
Organizational Affiliation
National Heart & Lung Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Heart & Lung Institute Clinical Studies Unit
City
London
ZIP/Postal Code
SW3 6HP
Country
United Kingdom

12. IPD Sharing Statement

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The Effects of OC000459 on Nasal Mediators

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