Walnut Oral Immunotherapy for Tree Nut Allergy
Peanut Allergy
About this trial
This is an interventional treatment trial for Peanut Allergy focused on measuring Interventional, Randomized, Double blind, Placebo controlled, Pediatric
Eligibility Criteria
Inclusion Criteria:
- Age 6 to 21 years, either sex, any race, any ethnicity with a convincing clinical history of walnut or another tree nut allergy and either a positive prick skin test (>3mm) or serologic evidence of allergic sensitization (defined as specific IgE>0.35 kU/L) to walnut and at least one other tree.
- A positive <2000 mg protein oral food challenge at enrollment to walnut and to one other tree nut.
- Written informed consent from participant and/or parent/guardian, including assent where indicated.
- All females of child-bearing age must be using appropriate birth control or practicing abstinence.
Exclusion Criteria:
- History of severe anaphylaxis to walnut or other tree nuts, defined as symptoms associated with hypoxia, hypotension or neurologic compromise (cyanosis or SpO2<92% at any stage, hypotension, confusion, collapse, loss of consciousness; or incontinence).
- Known allergy to oat
- Chronic disease (other than asthma, atopic dermatitis, rhinitis) requiring therapy or other respiratory or medical conditions deemed by the investigator to put subject at increased risk of anaphylaxis or poor outcomes from receiving OIT or undergoing food challenge.
- Poor control or persistent activation of atopic dermatitis
- Active eosinophilic or other inflammatory (e.g., celiac) gastrointestinal disease in the past 2 years.
- Participation in any interventional study for food allergy in the past 6 months
- Participant is on "build-up phase" of immunotherapy (i.e., has not reached maintenance dosing).
- Severe asthma (2007 NHLBI Criteria Steps 5 or 6, see Appendix 2)
- Mild or moderate (2007 NHLBI Criteria Steps 1-4) asthma with any of the following criteria met:
- FEV1 < 80% of predicted, or FEV1/FVC < 75%, with or without controller medications or
- ICS dosing of > 500 mcg daily fluticasone (or equivalent inhaled corticosteroids based on NHLBI dosing chart) or
- History of daily oral steroid dosing for > 1 month during the past year or
- Burst of oral, IM, or IV steroids for >3 days in the past 6 months for asthma control or
- > 1 burst of oral, IM or IV steroids in the past year for asthma control or
- > 1 hospitalization in the past year for asthma or
- > 1 ER visit in the past 6 months for asthma
- Inability to discontinue antihistamines for initial day escalation, skin testing or OFC
- Use of omalizumab or other non-traditional forms of allergen immunotherapy (e.g., oral or sublingual) or immunomodulator therapy (not including corticosteroids) or biologic therapy within the past year
- Use of beta-blockers (oral), angiotensin-converting enzyme (ACE) inhibitors, angiotensin-receptor blockers (ARB) or calcium channel blockers
Sites / Locations
- Children's Hospital of Philadelphia
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
walnut powder
placebo arm
Subjects will be randomized in a 2:1 ratio into either an active treatment group (final dose 1500 mg walnut protein, n=20) or a placebo group (n=10). Subjects will undergo a one-day desensitization protocol designed to enable the subject to tolerate 6 mg of walnut protein or placebo (initial day escalation phase). After the initial escalation day achieving at least 1.5 mg and up to 6 mg of walnut protein or placebo, dosing build-up will occur every two weeks through dose 24 at 34 weeks. A maintenance dose will be given for 4 weeks followed by a 5 gram protein OFC to walnut and a 5 gram protein OFC to a second tree nut (at ~38 weeks), after which the study will be unblinded.
Subjects will be randomized in a 2:1 ratio into either an active treatment group (final dose 1500 mg walnut protein, n=20) or a placebo group (n=10). Subjects will undergo a one-day desensitization protocol designed to enable the subject to tolerate 6 mg of walnut protein or placebo (initial day escalation phase). After the initial escalation day achieving at least 1.5 mg and up to 6 mg of walnut protein or placebo, dosing build-up will occur every two weeks through dose 24 at 34 weeks. A maintenance dose will be given for 4 weeks followed by a 5 gram protein OFC to walnut and a 5 gram protein OFC to a second tree nut (at ~38 weeks), after which the study will be unblinded. Placebo subjects that fail the OFC will be crossed over to active treatment and escalated as described to the 1500 mg target dose.