Food Allergy Clinical Trial
Official title:
Oral Desensitization to Egg With Subsequent Induction of Sustained Unresponsiveness for Egg-Allergic Children Using Baked Egg or Egg Oral Immunotherapy (OIT)
The purpose of this study is to compare Baked Egg vs. Egg Oral Immunotherapy for inducing sustained unresponsiveness to egg exposure in children.
Food allergy affects 6-8 percent of children in the United States. In young children,
reactions to egg can range from hives to severe life threatening allergic reactions called
anaphylaxis. Current treatment for food allergy is complete avoidance of the food and to
carry antihistamines and self-injectable epinephrine if an accidental reaction occurs.
However, accidental exposure to allergens in processed foods may be difficult to avoid.
Currently, several therapeutic strategies are being investigated to prevent and treat food
allergies. Since immunotherapy injections for food allergy are associated with a high rate of
allergic reactions, alternate approaches to treatment are needed. Oral (by mouth)
immunotherapy (OIT) is one approach that has been tried in some studies in the treatment of
food allergies. The purpose of this study is to compare baked foods with egg versus (vs.) egg
OIT. The intent of the study is to investigate if participants will be able to consume egg
after taking baked foods with egg or egg OIT for a period of time and then stopping for a
certain period. This is referred to as tolerance or sustained unresponsiveness. This study
will evaluate the effectiveness of the egg OIT vs. baked egg by having each participant
ingest egg white solid or baked foods with egg. This will be done over 2 years.
This study will last 2 years. All eligible subjects will receive a baked egg oral food
challenge (OFC). Those who pass the baked egg OFC will then have a 2 gm egg OFC. Those who
react to the egg OFC will be randomized to Baked Egg or Egg OIT. Individuals who do not pass
the initial baked egg OFC will be assigned to Egg OIT. Those who pass the egg OFC will not be
eligible for the study and will be followed per site standard of care. All eligible and
enrolled subjects will have a 1-year and a 2-year OFC.
At selected visits, blood and urine collection, physical examination, prick skin tests, and
atopic dermatitis and asthma evaluations will occur.
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