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Tolerance Results and Immune Mechanisms in Cow´s Milk and/or Hen´s Egg Allergic Children Following Natural Evolution or Oral Immunotherapy

RecruitingPhase 1, Phase 2Ages 4 Years - 17 YearsAllFundación de Investigación Biomédica - Hospital U…
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In plain words

What the trial is, and whether it could suit you

Allergy to Cow's milk and hen´s egg proteins are the most common causes of food allergies in early childhood and are associated with the occurrence of adverse events that may be life-threatening, quality of life impairment and negative nutritional and health economic impact. However, contrarily to other food allergy models such as nuts/peanut allergy, milk and egg allergy have greater chances of natural resolution. While around 50% of children may outgrow milk or egg allergy by the age of 5 years old, only 22% of peanut allergic children at the age of 4 years can tolerate this food. However, it is also documented that, at 14 years of age, the persistence of milk and egg allergy still affects around 30% of these children. Standard of care relies on food avoidance and treatment of accidental reactions, but this approach is unsatisfactory because adverse events and quality of life limitat

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📋 Eligibility rules (as published)
Inclusion Criteria: NAT-cohort: * Cow´s Milk and/or Hen´s Egg allergic patients 4 to 10 years old * sIgE levels to milk OR egg extracts between 0.35 to 35kUA/L * Positive entry Open food challenge with milk/egg with oFASS5 classification ≥2 with a maximum cumulative dose of up to 4193.7 mg of milk protein or 3110.8 mg of egg white protein * Having a mild to moderate food allergy severity per the Definition of Food Allergy Severity (DEFASE) score (\<13 points) * Having signed the informed consent OIT-cohort: * Patients in the compITO study (NCT06976775) who are undergoing OIT and have achieved full desensitization to the food by month 7 of the study (end of study) * Patients in the compITO study who are undergoing OIT and have achieved partial desensitization (tolerating a dose lower than the total dose, and a minimum of 3 doses above the entry challenge threshold) to the food by month 7 of the study (end of study) * Having signed the informed consent Exclusion Criteria: NAT-cohort: * Positive reaction in the entry open oral food challenge with a baseline Eliciting Dose (ED) 20 below the target ED20 for food. For milk, 23.1 mg (35.7 mg cumulative) of protein, or for egg, 19.5 mg (29.4 mg cumulative) of protein. * Patient desire or medical indication to initiate OIT at any time within 29 months of study entry. * No allergic reaction greater than oFASS5 grade 1 in the baseline challenge for the maximum cumulative programmed doses of 4193.7 mg of milk protein, or 3110.8 mg of egg white protein. * Immunological diseases, immunomodulatory/blocking therapies. * Severe atopic dermatitis according to the SCORing Atopic Dermatitis (SCORAD) classification * Severe allergy, according to a DEFASE score ≥13 * Spirometry values with moderate-to-severe airflow obstruction (FEV1 \<70%) * Poorly controlled asthma according to clinical criteria * Previous OIT for another food * Within the first 3 months of treatment with Subcutaneous Aeroallergen Immunotherapy * Within the first week of treatment with Sublingual Aeroallergen Immunotherapy * Presence or suspicion of Eosinophilic Esophagitis * Non-IgE-mediated allergy to milk or egg * Pregnancy * Significant medical comorbidities (renal, hepatic, or cardiac insufficiency, active infectious diseases, previous or concurrent cancers) * Inability to provide informed consent * Communication or cognitive barriers that prevent adherence to the protocol OIT-cohort: * Patients enrolled in the compITO study who have failed or withdrawn from the study for any reason. * Patients with uncontrolled Atopic Dermatitis or Asthma at the time of enrolment, or who have developed Eosinophilic Esophagitis. * Patients with confirmed pregnancy at the time of enrolment. * Patients who have developed significant medical comorbidities (renal, hepatic, or cardiac insufficiency, active infectious diseases, previous or concurrent cancers) at the time of enrolment. * Inability to provide informed consent. * Communication or cognitive barriers that prevent adherence to the protocol.
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What it tests

  • Oral Immunotherapy
  • Allergenic food avoidance
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Where

1 site
Hospital Infantil Universitario Niño Jesús. Avenida de Menéndez Pelayo, número 65
Madrid, Spain
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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