search
Back to results

Immunological Mechanisms of Oralair® in Patients With Seasonal Allergic Rhinitis

Primary Purpose

Allergic Rhinitis

Status
Completed
Phase
Phase 4
Locations
Australia
Study Type
Interventional
Intervention
Grass pollen sublingual immunotherapy tablet
Control
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 Allergic rhinitis, Asthma, Regulatory T cells, IgE, IgG4

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects of Chinese heritage or non-Chinese heritage
  • Clinical diagnosis of moderate to severe seasonal allergic rhinitis
  • Ryegrass-specific IgE : CAP-Pharmacia score > 1

Exclusion Criteria:

  • Ongoing immunotherapy or previous immunotherapy (within last 5 years)
  • Continuous oral corticosteroids
  • Moderate, severe or unstable asthma
  • Standard contraindications for allergen immunotherapy
  • Ongoing treatment with β-blockers
  • Immunodeficiency diseases
  • Malignancy
  • Significant inflammatory condition or disease in the oral cavity

Sites / Locations

  • Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital- Bayside Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Grass pollen sublingual immunotherapy tablet

Control

Arm Description

A sublingual allergen immunotherapy tablet (Oralair) containing: 300 index of reactivity (IR) of 5 grass pollen allergen extracts:perennial ryegrass (Lolium perenne), meadow grass (Poa pratensis), timothy grass (Phleum pratense), cocksfoot (Dactylis glomerata) and sweet vernal grass (Anthoxanthum odoratum) in an open label fashion administered for 4 months prior to the pollen season.

Standard medical therapy: oral antihistamines AND/OR nasal steroids AND/OR nasal antihistamines

Outcomes

Primary Outcome Measures

Change from Baseline in Ryegrass specific-IgG4 at 4 months and 12 months

Secondary Outcome Measures

Change in Quality of Life assessed by an Allergic Rhinitis Quality of Life Questionnaire at 4, 8 and 12 months
Change in Combined Symptoms and Medication requirements score at 4, 8 and 12 months
Change in Fractional Exhaled Nitric Oxide at 4, 8, and 12 months
Change in Helper and regulatory T cell response to ryegrass pollen at 4 months and 12 months
Change in Ryegrass-specific IgE at 4 months and 12 months

Full Information

First Posted
November 19, 2013
Last Updated
October 12, 2020
Sponsor
Bayside Health
search

1. Study Identification

Unique Protocol Identification Number
NCT02014623
Brief Title
Immunological Mechanisms of Oralair® in Patients With Seasonal Allergic Rhinitis
Official Title
Immunological Mechanisms of Oralair® (5 Grass Mix Sublingual Allergen Immunotherapy Tablet) in Patients With Seasonal Allergic Rhinitis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
November 15, 2019 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Allergic diseases represent a major health issue worldwide and epidemiological studies in Melbourne, Australia, have reported a high prevalence of rhinitis (hayfever) and atopy (genetic tendency to make allergy antibody) in Asian and Caucasian subjects. Mainstay treatment of allergic rhinitis 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 the sublingual route (SLIT) and recently sublingual tablets for pollen allergy immunotherapy became available. The tablets are safe and easy to use and contain pollen extracts from 5 of the most common allergy-causing European grasses but include ryegrass (Lolium perenne), the major seasonal pollen for allergy in Melbourne and south-eastern Australia. The immunological mechanisms of sublingual immunotherapy are not fully understood. The investigators propose conducting a longitudinal open label study to investigate the immunological changes that occur with the 5 grass pollen sublingual immunotherapy tablet (Oralair®) in a cohort of Chinese and non-Chinese background subjects. The investigators will investigate the induction of relevant T cell regulatory immune mechanisms and changes in serum allergen-specific immunoglobulin (Ig) E and IgG4. Immunoregulatory cytokine synthesis and T cell phenotype (Bio-plex and flow cytometry) will be examined. This project will provide important fundamental knowledge on which to inform decisions for the greater application of this treatment for subjects with moderate and severe allergic rhinitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis
Keywords
Allergic rhinitis, Asthma, Regulatory T cells, IgE, IgG4

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
51 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Grass pollen sublingual immunotherapy tablet
Arm Type
Active Comparator
Arm Description
A sublingual allergen immunotherapy tablet (Oralair) containing: 300 index of reactivity (IR) of 5 grass pollen allergen extracts:perennial ryegrass (Lolium perenne), meadow grass (Poa pratensis), timothy grass (Phleum pratense), cocksfoot (Dactylis glomerata) and sweet vernal grass (Anthoxanthum odoratum) in an open label fashion administered for 4 months prior to the pollen season.
Arm Title
Control
Arm Type
Other
Arm Description
Standard medical therapy: oral antihistamines AND/OR nasal steroids AND/OR nasal antihistamines
Intervention Type
Other
Intervention Name(s)
Grass pollen sublingual immunotherapy tablet
Intervention Type
Drug
Intervention Name(s)
Control
Other Intervention Name(s)
Oral anthistamines AND/OR Nasal steroids AND/OR Nasal antihistamines
Primary Outcome Measure Information:
Title
Change from Baseline in Ryegrass specific-IgG4 at 4 months and 12 months
Time Frame
Baseline, 4 months, 12 months
Secondary Outcome Measure Information:
Title
Change in Quality of Life assessed by an Allergic Rhinitis Quality of Life Questionnaire at 4, 8 and 12 months
Time Frame
Baseline, 4 months, 8 months, 12 months
Title
Change in Combined Symptoms and Medication requirements score at 4, 8 and 12 months
Time Frame
Baseline, 4 months, 8 months, 12 months
Title
Change in Fractional Exhaled Nitric Oxide at 4, 8, and 12 months
Time Frame
Baseline, 4 months, 8 months, 12 months
Title
Change in Helper and regulatory T cell response to ryegrass pollen at 4 months and 12 months
Time Frame
Baseline,4 months, 12 months
Title
Change in Ryegrass-specific IgE at 4 months and 12 months
Time Frame
Baseline, 4 months, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects of Chinese heritage or non-Chinese heritage Clinical diagnosis of moderate to severe seasonal allergic rhinitis Ryegrass-specific IgE : CAP-Pharmacia score > 1 Exclusion Criteria: Ongoing immunotherapy or previous immunotherapy (within last 5 years) Continuous oral corticosteroids Moderate, severe or unstable asthma Standard contraindications for allergen immunotherapy Ongoing treatment with β-blockers Immunodeficiency diseases Malignancy Significant inflammatory condition or disease in the oral cavity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robyn O'Hehir, MBBS MBBS FRACP FRCP PhD
Organizational Affiliation
Director, Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Hew, MBBS FRACP PhD
Organizational Affiliation
Head of Allergy, Asthma and Clinical Immunology Service, Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jennifer Rolland, BSc, PhD
Organizational Affiliation
Emeritus Professor Central Clinical School Monash University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Alessandra Sandrini, MD, PhD
Organizational Affiliation
Senior Clinical Fellow, Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Celia Zubrinich, MBBS FRACP
Organizational Affiliation
Consultant, Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nirupama Varese, BSc Hons, MSc
Organizational Affiliation
Research Officer, Central Clinical School Monash University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Allergy, Immunology and Respiratory Medicine, The Alfred Hospital- Bayside Health
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3181
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
29461859
Citation
O'Hehir RE, Varese NP, Deckert K, Zubrinich CM, van Zelm MC, Rolland JM, Hew M. Epidemic Thunderstorm Asthma Protection with Five-Grass Pollen Tablet Sublingual Immunotherapy: A Clinical Trial. Am J Respir Crit Care Med. 2018 Jul 1;198(1):126-128. doi: 10.1164/rccm.201711-2337LE. No abstract available.
Results Reference
derived

Learn more about this trial

Immunological Mechanisms of Oralair® in Patients With Seasonal Allergic Rhinitis

We'll reach out to this number within 24 hrs