GUPI: The Grown Up Peanut Immunotherapy Study
Study Details
Study Description
Brief Summary
To determine efficacy and safety of peanut oral immunotherapy in adults with peanut allergy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
25 adults with peanut allergy, as confirmed by double blind placebo controlled food challenge (DBPCFC), will undergo peanut oral immunotherapy (OIT) with peanut flour.
An additional 15 untreated peanut allergic adults will be recruited as comparator group for skin prick tests and mechanistic studies/immunological assays.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Peanut oral immunotherapy Desensitisation using peanut flour |
Other: Peanut oral immunotherapy
Daily doses of peanut flour (with 2-weekly incremental interval)
|
Outcome Measures
Primary Outcome Measures
- Desensitisation to 1.4g peanut [7-8 months]
Tolerance of cumulative dose of 1.4g peanut protein without reaction on DBPCFC post OIT after minimum of 1 month maintenance dosing on peanut OIT
Secondary Outcome Measures
- Desensitisation to 4.4g peanut [7-8 months]
Tolerance of cumulative dose of 4.4 g peanut protein without reaction on DBPCFC post OIT
- Incidence of adverse events related to treatment (safety) [7-8 months]
Incidence of local and systemic reactions during peanut OIT updosing and maintenance
- Reactions with ara h 8 sensitisation [7-8 months]
Comparison of local and systemic reactions in Ara h 8 sensitised vs. non-sensitised subjects.
- Skin prick test reactivity [9 months]
Change in size of wheal diameter to peanut extract following OIT
- Immunoglobulin G (IgG) levels [9 months]
Change in peanut-specific IgG following OIT
- Quality of life measure [7-8 months]
Change measured using Food Allergy Quality of Life Questionnaire- Adult Form (FAQLQ-AF) and the Food Allergy Independent Measure Adult Form (FAIM-AF). These are validated questionnaires consisting of 29 (FAQLQ-AF) and 6 (FAIM-AF) questions each scored on a 7 point likert scale. The total scores are the mean score of all items with a range of 1 'no impairment' to 7 'maximal impairment'.
- Food Neophobia score [7-8 months]
Change measured using validated Food Neophobia Scale (FNS) questionnaire. This consists of 8 questions with answers on a 7 point likert scale ranging from 1 ("disagree strongly") to 7 ("agree strongly"). The total score is the mean score of all questions with lower score signifying increased food neophobia.
- Food Situations score [7-8 months]
Change using Food Situations Questionnaire, validated in children and amended to be appropriate for adults. 10 different scenarios related to food are rated from 1 (very unhappy) to 5 (very happy), giving a total possible score of 50. Higher scores are indicative of lower food neophobia.
- Study compliance [7-8 months]
Compliance with OIT measured using monthly diaries.
Eligibility Criteria
Criteria
Inclusion Criteria:
For peanut OIT patients:
Adults aged 18-40 years with:
-
A positive skin prick test to peanut extract.
-
Elevated (>0.35) serum specific Immunoglobulin E (IgE) to Ara h 2 major peanut allergen within 2 years of date of initial screening visit.
-
Positive DBPCFC to 300mg or less of peanut protein.
-
Where appropriate, use of effective form of birth control by females for the duration of participation in the study (i.e. up to exit DBPCFC).
-
Participants with asthma may be included if well controlled:
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Asthma control questionnaire (ACQ) score <1
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Maximum permitted asthma treatment: moderate dose of inhaled corticosteroid (ICS) and long-acting beta agonists (LABA) as treatment
-
Pre-bronchodilator Forced Expiratory Volume in 1 second (FEV1) >80% of predicted value at screening visit
-
For asthmatic participants with intermittent mild symptoms (induced by exercise, animals or pollens) using as required salbutamol only, treatment will be given with regular low dose inhaled corticosteroids (ICS) prior to challenges and for the duration of updosing as an additional measure.
For mechanistic sub-study subjects:
Adults aged 18-40 years with:
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A positive skin prick test to peanut extract within previous 12 months
-
Elevated serum specific IgE (>0.35) to Ara h 2 major peanut allergen within 2 years of date of initial screening visit.
-
Clinical diagnosis of peanut allergy made by an experienced allergy specialist.
Exclusion Criteria:
For peanut OIT patients:
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Anaphylaxis to a food other than peanut - despite attempted avoidance - within the last 2 years.
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History of life-threatening anaphylaxis or angioedema, including previous intensive care unit (ITU) admission attributable peanut allergy.
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Asthmatic treated with higher than moderate dose of ICS (>800 mcg equivalent of beclomethasone dipropionate (BDP) per day).
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Any asthmatic if uncontrolled or difficult to control as evidenced by any following: ACQ>1; FEV1 <80% predicted; FEV1/ forced vital capacity (FVC) <0.7 irrespective of treatment; hospital attendance (A&E or admission) for asthma in the past 2 years; treatment of asthma with oral steroids within last 2 years.
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Evidence of non-adherence with asthma treatment from General PRactitioner (GP) repeat prescription records.
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Participants who react to less than 1 mg of peanut protein on DBPCFC, or who cannot tolerate at least an initial dose of 1.5 mg peanut protein on OIT initiation day.
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Participants who react to placebo during DBPCFC.
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Ongoing treatment with beta-blockers, biologics (such as omalizumab or mepolizumab) or systemic immunosuppressive treatment.
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Regular ongoing use of NSAIDs for a chronic condition (NSAIDs may act as a co-factor for allergic reactions)
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For females a positive serum or urine pregnancy test with sensitivity of less than 50 mIU/mL within 72 hours of first administration of study therapy.
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Lactating females.
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The use of any investigational drug within 30 days of the screening visit.
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Past history of eosinophilic oesophagitis or chronic gastro-oesophageal reflux symptoms requiring regular treatment with anti-acids.
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Inability to discontinue antihistamines for a minimum of 4 days prior to DBPCFC visits
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The presence of any medical condition that the investigator deems incompatible with participation in the trial.
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Individuals with insufficient understanding of the trial.
For mechanistic sub-study subjects:
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Ongoing treatment with biologic or systemic immunosuppressive treatment.
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Known current pregnancy
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Lactating females.
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The use of any investigational drug within 30 days of the screening visit.
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Inability to discontinue antihistamines for a minimum of 4 days prior to venesection.
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The presence of any medical condition that the investigator deems incompatible with participation in the study.
-
Individuals with insufficient understanding of the study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Guy's and St Thomas' NHS Foundation Trust | London | United Kingdom | SE1 9RT |
Sponsors and Collaborators
- Guy's and St Thomas' NHS Foundation Trust
- National Institute for Health Research, United Kingdom
- King's College London
- Imperial College London
Investigators
- Principal Investigator: Stephen J Till, MA FRCP PhD, Guy's and St Thomas' NHS Foundation Trust / King's College London
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 225583