Boiled Peanut Immunotherapy for the Treatment of Peanut Allergy (BOPI-2)

Imperial College London

Status: Active, not recruiting

Conditions: IgE Mediated Peanut Allergy; Peanut Hypersensitivity

Treatments: Other: Defatted roasted peanut flour; Other: Boiled peanut

Study type: Interventional

Funder types: Other

Identifiers

NCT03937726

19SM5033

Details and patient eligibility

About

Peanut allergy is the most common cause of severe allergic reactions to food. Onset is common in childhood, but in contrast to other food allergies such as cow's milk and egg, peanut allergy tends to persist into adulthood. It is associated with a significant impact on quality of life, both for the affected individual and their family.

There is no current cure for peanut allergy. Oral peanut immunotherapy (OIT) using defatted, roasted peanut flour has been demonstrated to offer potential in this regard, but is associated with significant and frequent reactions and can cause life-threatening allergic symptoms.

The investigators have previously demonstrated that the processing of peanuts through boiling results in a relatively hypoallergenic product due to the loss of key allergenic components from peanut into the water. This has been tested in a recently-completed Phase 2b/3 trial (The BOPI Study, Clinicaltrials.gov NCT02149719; HRA reference 15/LO/0287): 47 children/ young people with peanut allergy confirmed at double-blind, placebo-controlled food challenge (DBPCFC) were randomised (2:1) to receive either oral immunotherapy (updosing using boiled peanut for ~6 months, followed by maintenance with roasted peanut) or standard treatment (allergen avoidance). Participants underwent repeat DBPCFC at 12 months to assess response, following which peanut OIT was stopped and sustained unresponsiveness assessed after 4 weeks (4SU). 24/32 participants (100% per protocol) achieved the primary outcome of desensitisation to >1.44g peanut protein (approximately 6-8 peanuts, p<0.0001); of those 14 tolerated >4.4g peanut protein. 13/24 participants achieved 4SU. There was no significant change in threshold in the control group (p>0.05). Boiled peanut OIT had a favourable safety profile, with under 2% of doses associated with gastrointestinal symptoms.

The BOPI-2 study is a non-inferiority study to demonstrate that boiled peanut is at least as effective as peanut flour in treating children with peanut allergy. The study will compare the rate of adverse events and other safety outcomes between these two interventions, and assess the immunological mechanisms involved, a secondary aim being to develop clinically-useful predictors for identifying individuals likely to undergo successful desensitisation.

Enrollment: 83 patients

Sex: All

Ages: 7 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 7-18 years (enrolment up to a participant's 19th birthday).
• Past history consistent with IgE-mediated peanut allergy
• Allergic to ≤1.44 g peanut protein (approx. 6 peanuts) at baseline double-blind placebo-controlled food challenge, prior to treatment allocation
• Tolerates at least 1/8 boiled peanut (boiled for 4 hours) at open food challenge at screening.
• Written informed consent of parent/legal guardian and patient assent.

Exclusion criteria

• Required previous admission to an intensive care unit for management of an allergic reaction to peanut.
• Clinically significant chronic illness (other than asthma, rhinitis or eczema).
• Undergoing subcutaneous or sublingual immunotherapy to respiratory allergens, and not yet established on maintenance dosing for at least 3 months.
• Undergoing oral immunotherapy for food allergy and within the first year of treatment.
• Subjects receiving anti-IgE therapy, oral immunosuppressants, beta-blocker or ACE inhibitor.
• Tolerance to ≥1.44 g peanut protein (approx. 6 peanuts) at initial DBPCFC during screening.
• Dose-limiting symptoms to 1/8 boiled peanut (boiled for 4 hours) at screening.
• Poorly controlled asthma within the previous 3 months (as defined by clinician judgement with reference to the ICON consensus ), or asthma requiring treatment with >5 days oral corticosteroids within the previous 3 months.
• Pregnancy
• Unwilling or unable to fulfil study requirements

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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83 participants in 2 patient groups

Boiled peanut Oral Immunotherapy

Experimental group

Description:

Desensitisation using boiled peanut

Treatment:

Other: Boiled peanut

Conventional Oral immunotherapy

Active Comparator group

Description:

Desensitisation using defatted peanut flour

Treatment:

Other: Defatted roasted peanut flour