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A Trial of Immunological Outcomes of Sublingual Immunotherapy for House Dust Mite (D. Pteronyssinus) Allergy

Primary Purpose

Allergic Rhinitis, Asthma

Status
Completed
Phase
Phase 4
Locations
Australia
Study Type
Interventional
Intervention
(agent for immunotherapy) Staloral
Placebo
Sponsored by
Bayside Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Allergic Rhinitis focused on measuring rhinitis, asthma, atopy, house dust mite, immunotherapy, SLIT

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: allergic rhinitis and/or mild stable asthma house dust mite allergic positive HDM-specific IgE as determined by skin prick test (wheal diameter >6 mm to D. pteronyssinus) or CAP-Pharmacia score > 2 Exclusion Criteria: Immunodeficiency diseases Severe or uncontrolled asthma Previous immunotherapy with House dust mite (HDM) extract within the last five years or ongoing immunotherapy with HDM or other allergens Continuous oral corticosteroids Subjects on treatment with beta-blockers Pregnant women

Sites / Locations

  • The Alfred Hospital. Department of Allergy Immunology & Respiratory Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

1

2

Arm Description

Matching placebo- control arm (first year)

Drug Staloral (active group)

Outcomes

Primary Outcome Measures

Immunological mechanisms of SLIT by phenotyping different subsets of cytokine positive T cells, regulatory T cells, and memory T cells in peripheral blood of subjects before, during and after immunotherapy.
-Expression of "immunoregulatory" cytokines by CD4+ T
cells
- Helper, regulatory and memory T cell subsets
(a) Helper T cells
(b) Regulatory T cells
b1- Regulatory T cell phenotype
b2- Regulatory T cell function

Secondary Outcome Measures

Symptom diary, medication use, visual analogue score, disease-specific rhinoconjunctivitis Quality of Life Questionnaire

Full Information

First Posted
November 6, 2005
Last Updated
February 11, 2013
Sponsor
Bayside Health
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1. Study Identification

Unique Protocol Identification Number
NCT00250263
Brief Title
A Trial of Immunological Outcomes of Sublingual Immunotherapy for House Dust Mite (D. Pteronyssinus) Allergy
Official Title
A Trial of Immunological Outcomes of Sublingual Immunotherapy for House Dust Mite (D. Pteronyssinus) Allergy
Study Type
Interventional

2. Study Status

Record Verification Date
November 2005
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bayside Health

4. Oversight

5. Study Description

Brief Summary
Allergic diseases represent a major health issue worldwide. Mainstay treatment is allergen avoidance and pharmacotherapy for symptom relief. Allergen immunotherapy offers the advantages of specific treatment with long lasting efficacy, and can modify the course of disease. However, use of this treatment is restricted by the high risk of adverse events especially in asthmatics. Other, better tolerated, routes of allergen administration than the current conventional subcutaneous route (SCIT) have been investigated including sublingual (SLIT). However, the immune parameters of SLIT have not been examined. We propose conducting a randomised, placebo-controlled study of a commercially-available SLIT for house dust mite (HDM) allergy to investigate induction of relevant T cell regulatory immune mechanisms. The first year will be followed by an optional open label extension period. Immunoregulatory cytokine synthesis and T cell phenotype and function (real time PCR and flow cytometry) will be examined. This project will provide important fundamental knowledge on which to base improved and greater application of this potentially curative treatment for allergy. SLIT has the potential advantage of home administration and suitability for patients with asthma who are currently unable to access many of the allergen desensitising regimens.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis, Asthma
Keywords
rhinitis, asthma, atopy, house dust mite, immunotherapy, SLIT

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Placebo Comparator
Arm Description
Matching placebo- control arm (first year)
Arm Title
2
Arm Type
Active Comparator
Arm Description
Drug Staloral (active group)
Intervention Type
Drug
Intervention Name(s)
(agent for immunotherapy) Staloral
Intervention Description
Immunotherapy agent for sublingual daily use. First week (vial containing the concentration 10 IR/ml) Day 1 - 1 pressure Day 2 - 2 pressures Day 3 - 4 pressures Day 4 - 6 pressures Day 5 - 8 pressures Day 6 - 10 pressures Second week (300 IR/ml) (vial containing the concentration 300 IR/ml) Day 7 - 1 pressure Day 8 - 2 pressures Day 9 - 4 pressures Day 10 - 6 pressures Day 11 - 8 pressures Maintenance phase Day 12 to 364 - 8 pressures daily The first year will be followed by a second year open label period (optional)- 8 pressures daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matching placebo for sublingual use. Same schedule used for the intervention ACTIVE group. First week (vial containing placebo) Day 1 - 1 pressure Day 2 - 2 pressures Day 3 - 4 pressures Day 4 - 6 pressures Day 5 - 8 pressures Day 6 - 10 pressures Second week (300 IR/ml) (vial containing placebo) Day 7 - 1 pressure Day 8 - 2 pressures Day 9 - 4 pressures Day 10 - 6 pressures Day 11 - 8 pressures Maintenance phase Day 12 to 364 - 8 pressures daily
Primary Outcome Measure Information:
Title
Immunological mechanisms of SLIT by phenotyping different subsets of cytokine positive T cells, regulatory T cells, and memory T cells in peripheral blood of subjects before, during and after immunotherapy.
Time Frame
12 and 24 months
Title
-Expression of "immunoregulatory" cytokines by CD4+ T
Time Frame
12 and 24 months
Title
cells
Time Frame
12 and 24 months
Title
- Helper, regulatory and memory T cell subsets
Time Frame
12 and 24 months
Title
(a) Helper T cells
Time Frame
12 and 24 months
Title
(b) Regulatory T cells
Time Frame
12 and 24 months
Title
b1- Regulatory T cell phenotype
Time Frame
12 and 24 months
Title
b2- Regulatory T cell function
Time Frame
12 and 24 months
Secondary Outcome Measure Information:
Title
Symptom diary, medication use, visual analogue score, disease-specific rhinoconjunctivitis Quality of Life Questionnaire
Time Frame
12 and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: allergic rhinitis and/or mild stable asthma house dust mite allergic positive HDM-specific IgE as determined by skin prick test (wheal diameter >6 mm to D. pteronyssinus) or CAP-Pharmacia score > 2 Exclusion Criteria: Immunodeficiency diseases Severe or uncontrolled asthma Previous immunotherapy with House dust mite (HDM) extract within the last five years or ongoing immunotherapy with HDM or other allergens Continuous oral corticosteroids Subjects on treatment with beta-blockers Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robyn O'Hehir, MD FRACP FRCP PhD
Organizational Affiliation
Alfred Hospital; Monash University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jennifer Rolland, PhD
Organizational Affiliation
Alfred Hospital; Monash University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jo Douglass, MBBS FRACP MD
Organizational Affiliation
Alfred Hospital; Monash University
Official's Role
Study Chair
Facility Information:
Facility Name
The Alfred Hospital. Department of Allergy Immunology & Respiratory Medicine
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3181
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
10592467
Citation
Fanta C, Bohle B, Hirt W, Siemann U, Horak F, Kraft D, Ebner H, Ebner C. Systemic immunological changes induced by administration of grass pollen allergens via the oral mucosa during sublingual immunotherapy. Int Arch Allergy Immunol. 1999 Nov;120(3):218-24. doi: 10.1159/000024270.
Results Reference
background
PubMed Identifier
15298560
Citation
Gardner LM, Thien FC, Douglass JA, Rolland JM, O'Hehir RE. Induction of T 'regulatory' cells by standardized house dust mite immunotherapy: an increase in CD4+ CD25+ interleukin-10+ T cells expressing peripheral tissue trafficking markers. Clin Exp Allergy. 2004 Aug;34(8):1209-19. doi: 10.1111/j.1365-2222.2004.02009.x.
Results Reference
background
PubMed Identifier
11060692
Citation
Rolland JM, Douglass J, O'Hehir RE. Allergen immunotherapy: current and new therapeutic strategies. Expert Opin Investig Drugs. 2000 Mar;9(3):515-27. doi: 10.1517/13543784.9.3.515.
Results Reference
background
PubMed Identifier
19696440
Citation
O'Hehir RE, Gardner LM, de Leon MP, Hales BJ, Biondo M, Douglass JA, Rolland JM, Sandrini A. House dust mite sublingual immunotherapy: the role for transforming growth factor-beta and functional regulatory T cells. Am J Respir Crit Care Med. 2009 Nov 15;180(10):936-47. doi: 10.1164/rccm.200905-0686OC. Epub 2009 Aug 20.
Results Reference
derived

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A Trial of Immunological Outcomes of Sublingual Immunotherapy for House Dust Mite (D. Pteronyssinus) Allergy

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