MedPath

Peanut and Tree Nut Desensitization

Not Applicable
Active, not recruiting
Conditions
Tree Nut Allergy
Peanut Allergy
Interventions
Other: Oral immunotherapy
Registration Number
NCT03532360
Lead Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Brief Summary

this study evaluates whether tolerance to peanuts and tree nuts can be induced in patients through a process of oral immunotherapy. Participants will be randomized into groups receiving oral immunotherapy and a control group that will receive no intervention

Detailed Description

The investigators are proposing to initiate a study assessing a common desensitization protocol for peanut/tree nut allergy. This study would enable the investigators to better determine the potential benefit of desensitization in individuals with peanut/tree nut allergy.

More specifically, the investigators will address the following research objectives:

Objectives A. To develop a protocols for peanut/tree nut desensitization with high (300mg) and low (30mg maintenance dose).

B. To determine the rate of desensitization to peanut/tree nut. C. To characterize predictors of successful desensitization. D. To characterize molecular mechanisms involved in the process of desensitization

These objectives will be evaluated through a randomized controlled trial

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
51
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
High-doseOral immunotherapyFollowing randomization, participants in this group will receive escalating doses of the appropriate allergen, up to a dose of 300 mg. Once they attain that dose, they will maintain it for six months. At the end of this maintenance period, they will undergo a singe-blind, placebo-controlled oral food challenge
Low-doseOral immunotherapyFollowing randomization, participants in this group will receive escalating doses of the appropriate allergen, up to a dose of 30 mg. Once they attain that dose, they will maintain it for six months. At the end of this maintenance period, they will undergo a singe-blind, placebo-controlled oral food challenge
Primary Outcome Measures
NameTimeMethod
Efficacy of desensitization in peanut/tree nut allergic patients as measured by blinded, placebo controlled oral food challenge21 months

Comparison of participants randomized to treatments arms who achieve peanut/tree nut desensitization compared to participants randomized to the control groups. This is measured by whether a participant is able to tolerate a total dose of 4172 mg crushed peanut or tree nut during an oral food challenge

Comparison of efficacy of 30 mg dose versus 300 mg dose in inducing desensitization to peanut or tree nut as measured by blinded, placebo controlled oral food challenge21 months

Participants in the 30 mg arm will be compared to those in the 300 mg in terms of dose tolerated at post-immunotherapy blinded, placebo-controlled oral food challenge, as well as side effects experienced during immunotherapy

Secondary Outcome Measures
NameTimeMethod
Change from baseline over the immunotherapy process of peanut or tree nut (as appropriate) specigic IgE levels21 months

Measurement of peanut or tree nut (as appropriate) specific IgE before, during and after the desensitization process

Change from baseline over the immunotherapy process of peanut or tree nut (as appropriate) specigic IgA levels21 months

Measurement of peanut or tree nut (as appropriate) specific IgA before, during and after the desensitization process

Change from baseline over the immunotherapy process of peanut or tree nut (as appropriate) specigic IgG4 levels21 months

Measurement of peanut or tree nut (as appropriate) specific IgG4 before, during and after the desensitization process

Change from baseline over the immunotherapy process of mast cell activation as measured by CD63 expression21 months

Measurement of mast cell activation as measured by CD63 expression before, during and after the desensitization process

Change from baseline over the immunotherapy process of of DNA methylation levels21 months

Measurement of DNA methylation levels before, during and after the desensitization process

Change from baseline over the immunotherapy process of Regulatory T cell levels21 months

Measurement of Regulatory T cell levels, before, during and after the desensitization process

Trial Locations

Locations (2)

Montreal Children's Hospital

🇨🇦

Montreal, Quebec, Canada

Hospital for Sick Children

🇨🇦

Toronto, Ontario, Canada

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