Oral Immunotherapy for Food Protein Induced Enterocolitis Syndrome

NCT06614244 | Not Yet Recruiting

• 1 other identifier: 6563
• Study Type: interventional
• Target: 168
• Locations: 1 country
• Sites: 1

Brief Summary

Food Protein Induced Enterocolitis Syndrome (FPIES) is a food allergy characterized by clinical manifestations of varying severity that can be, very rarely, severe to the point of leading to shock. Acute FPIES is nowaday the most common presentation of the disease. It is characterized by repeated, projectile vomiting (usually arising between 1 and 4 hours after ingestion of the culprit food) accompanied by pallor, hypotonia, and lethargy, with complete resolution of the aforementioned symptoms almost always within a few hours. Dietary management of FPIES currently involves avoiding allergens, offering complementary foods to encourage normal growth and providing families with individualized feeding plans. The elimination diet does not promote healing, it only prevents adverse reactions from culprit food ingestion. Recovery (i.e. tolerance to the culprit food) is achieved spontaneously over time. However, for some children, tolerance does not occur. These patients suffer from persistent FPIES. For these patients oral immunotherapy (OIT) is not yet planned and randomized and controlled studies are needed to demonstrate its efficacy and safety. The primary objective of the study will be to verify, with a multicenter, prospective, randomized study, stratified for the main 4 offending foods in Italy (cows milk, hens egg, fish and cereals), open-label and with an adequate sample size, the efficacy and safety of an OIT procedure in children affected by acute persistent FPIES. The comparison will be made between a population of children affected by acute persistent FPIES subjected to OIT for the offending food (DOPA group) and a population of children affected by acute persistent FPIES subjected to the traditional measure, i.e. the elimination diet for the offending food (Diet group). Efficacy will be measured through:

• Comparison of the percentages of children who have increased their reactivity threshold even to the point of no adverse reactions to the offending food following the intake of a normal dose for their age in the two populations during treatment;
• Comparison of the percentages of children who have reached tolerance towards the culprit food in the two populations; Safety will be measured through: \- Comparison of the percentages of children who have presented adverse reactions following the ingestion (accidental in the Diet group and expected in the DOPA group) of the culprit food after enrollment in the study. The definitions of desensitization and tolerance are taken from the EAACI 2018 guidelines on immunotherapy for IgE-mediated AA. In particular, desensitization corresponds to the absence of adverse reactions following the ingestion of the culprit food (in quantities up to a normal dose for age) during oral immunotherapy. This is a reversible or partially reversible clinical response that depends on continued exposure to the allergen. If the administration of the allergen is interrupted, the previous level of clinical reactivity may return. Tolerance corresponds to the absence of adverse reactions following the ingestion of the culprit food despite a period of absence of exposure.

Conditions

FPIES

Outcome Measures

Primary Outcomes (1)

• Comparison of the percentages of participants who will achieve desensitization to the culprit food in the two populations

  Efficacy will be measured through comparison of the percentages of children who will have increased their threshold of reactivity to the incriminated food following the intake of a normal dose for their age, in the two study populations (Definition of desensitization and tolerance according to EAACI 2018 guidelines on immunotherapy for IgE-mediated AA)

  18 months

Secondary Outcomes (1)

• Phenotypic characteristics of the patient who responds to OIT

  18 months

Study Arms (2)

DOPA group

EXPERIMENTAL

Children affected by acute persistent FPIES subjected to OIT for the offending food

Procedure: Oral immunotherapy (OIT)

Diet group

ACTIVE COMPARATOR

Children affected by acute persistent FPIES subjected to the traditional measure, i.e. the elimination diet for the offending food

Dietary Supplement: Culprit food elimination diet

Interventions

Oral immunotherapy (OIT) PROCEDURE

OIT in DOPA group will be implemented as follows. Both the first micro-dose of the offending food and the subsequent micro-increments will be administered at home. Any interruptions and resumptions of OIT, due to intercurrent events (e.g. infections), will be managed via email with or without medical visit via video call. Patients will be provided with ondansetron (sublingual film) and instructions for its use. An explanatory letter will also be provided in case of need for emergency room access.

DOPA group

Culprit food elimination diet DIETARY_SUPPLEMENT

The Diet group consists of a population of children affected by acute persistent FPIES subjected to the traditional measure, i.e. the elimination diet of the incriminated food.

Diet group

Eligibility Criteria

• Age: 3 Years - 17 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Pediatric patients (under 18 years of age) affected by persistent acute food protein-induced enterocolitis syndrome.

You may not qualify if:

• Transition from acute FPIES to IgE-mediated AA.
• Absence of informed consent approval by their caregivers.
• Failure to use email by their caregivers.

Sponsors & Collaborators

• Fondazione Policlinico Universitario Agostino Gemelli IRCCS: lead

Study Sites (1)

Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Pediatria

Roma, 00168, Italy

Location

MeSH Terms

Interventions

Immunotherapy

Intervention Hierarchy (Ancestors)

Immunomodulation; Biological Therapy; Therapeutics

Study Officials

• Stefano Miceli Sopo

  Fondazione Policlinico Universitario A. Gemelli, IRCCS

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Stefano Miceli Sopo

CONTACT

+390630155701; Stefano.MiceliSopo@unicatt.it

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 2, 2024
• First Posted: September 26, 2024
• Study Start: October 1, 2024
• Primary Completion (Estimated): October 1, 2027
• Study Completion (Estimated): March 31, 2028
• Last Updated: September 26, 2024

Record last verified: 2024-08

Locations

IT (1)