Walnut Oral Immunotherapy for Tree Nut Allergy



Status:Not yet recruiting
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:6 - 45
Updated:5/3/2014
Start Date:May 2013
End Date:May 2018
Contact:Janet S Kamilaris, RN
Email:janet.kamilaris@unc.edu
Phone:919-962-4413

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The purpose of this study is to determine if walnut oral immunotherapy can be used in
subjects allergic to tree nuts to decrease their tree nut allergy and induce changes in
their immune system.

Tree nut

Inclusion Criteria:

- Age 6 to 45 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 nut.

- A positive 2000 mg oral food challenge at enrollment to walnut and to one other tree
nut.

- Written informed consent from participant and/or parent/guardian

- Written assent from all subjects as appropriate

- All females of child bearing age must be using appropriate birth control

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 the 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) or poorly controlled
mild or moderate 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

- Pregnancy or lactation
We found this trial at
1
site
CHapel Hill, North Carolina 27599
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CHapel Hill, NC
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