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Tolerability of Hypoallergenic Formula in Children With Cow's Milk Allergy (SINEALLII)

Primary Purpose

Allergy Milk

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
amino acid based formula
Sponsored by
Federico II University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Allergy Milk

Eligibility Criteria

1 Month - 36 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Consecutive patients aged 1-36 months with diagnosis of Immunoglobulin E-mediated cow milk allergy in the last 12 weeks,
  • full and stable remission of allergy symptoms
  • Written informed consent form collected by the parents.

Exclusion Criteria:

  • Infant aged <1 months and >36 months,
  • breast fed infants,
  • other food allergies,
  • other allergic diseases,
  • evidence of non-IgE-mediated CMA,
  • history of severe anaphylactic reaction,
  • eosinophilic disorders of the gastrointestinal tract,
  • chronic systemic diseases,
  • congenital cardiac defects,
  • active tuberculosis,
  • autoimmune diseases,
  • immunodeficiency,
  • chronic inflammatory bowel diseases,
  • celiac disease,
  • cystic fibrosis,
  • metabolic diseases,
  • malignancy,
  • chronic pulmonary diseases,
  • malformations of the gastrointestinal and/or respiratory tract,
  • use of systemic antibiotics or anti-mycotic drugs during 4 weeks before study entry;
  • investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements;
  • participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study.

Sites / Locations

  • Rita NocerinoRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

amino acid based formula

Arm Description

amino acid based formula

Outcomes

Primary Outcome Measures

Number of subjects tolerants to a new hypoallergenic formula demonstrated by oral food challenge with the new study formula
All subjects perform an oral food challenge with the new study formula. If the infant not react to the new hypoallergenic formula during the oral food challenge, the subjects tolerate this product.

Secondary Outcome Measures

Evaluation of body weight in children assuming amino acid based formula
In the absence of reaction to the new amino acid based formula, a subgroup of child (n=15) will continue the second part of the study, with an open-label feeding with amino acid based formula for 180 days.

Full Information

First Posted
April 5, 2019
Last Updated
April 8, 2019
Sponsor
Federico II University
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1. Study Identification

Unique Protocol Identification Number
NCT03909113
Brief Title
Tolerability of Hypoallergenic Formula in Children With Cow's Milk Allergy
Acronym
SINEALLII
Official Title
Tolerability of the New Hypoallergenic Formula in Children With IgE Mediated Cow's Milk Allergy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
April 30, 2020 (Anticipated)
Study Completion Date
May 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Cow's milk protein allergy is defined as an immunological reaction to one or more milk proteins. A variety of symptoms can be suggestive for cow's milk protein allergy . Cow's milk protein allergy is suspected clinically in 5-15% of infants, while most estimates of prevalence of cow's milk protein allergy vary from only 2 to 5 %. Confusion regarding cow's milk protein allergy prevalence is often due to differences in study populations, study design and a lack of defined diagnostic criteria. The importance of defined diagnostic criteria needs to be emphasised. It precludes infants from an unnecessary diet and avoids delay in diagnosis, which can lead to malnutrition. The treatment of cow's milk protein allergy is the dietary elimination of cow's milk proteins. In non-breastfed infants and children less than 2 years of age, a substitute formula is mandatory as prescribed by several international scientific societies. Extensively hydrolyzed formulas are used as therapeutic formulas. An extensively hydrolysed formula is often a whey or casein based formula in which the protein has been chopped up in smaller pieces that are less allergenic. Because of high cross-reactivity (up to 80%) and nutritional inadequacy, the use of any other animal milk or soy-based formula is precluded.The infant should be maintained on an elimination diet until the child is between 9-12 months of age or at least for 6 months, whichever occurs first. In most cases, symptoms will improve substantially within 2-4 weeks if diagnosis is correct. According to consensus in literature, a therapeutic formula is a formula tolerated by at least 90% (with 95% confidence) of cow's milk protein allergy infants. The primary study outcome will be the evaluation of the hypoallergenicity of a new aminoacid based formula in children with confirmed immunoglobulin (Ig)E- mediated CMA. According to the American Academy of Pediatrics (AAP) Subcommittee on Nutrition and Allergic Diseases a hypoallergenic formula must be tested in infants and children with hypersensitivity to cow's milk proteins, with findings verified by elimination-challenge tests under double-blind, placebo-controlled conditions (DBPCFC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergy Milk

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
29 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
amino acid based formula
Arm Type
Experimental
Arm Description
amino acid based formula
Intervention Type
Dietary Supplement
Intervention Name(s)
amino acid based formula
Intervention Description
amino acid based formula
Primary Outcome Measure Information:
Title
Number of subjects tolerants to a new hypoallergenic formula demonstrated by oral food challenge with the new study formula
Description
All subjects perform an oral food challenge with the new study formula. If the infant not react to the new hypoallergenic formula during the oral food challenge, the subjects tolerate this product.
Time Frame
After one week from the oral food challenge
Secondary Outcome Measure Information:
Title
Evaluation of body weight in children assuming amino acid based formula
Description
In the absence of reaction to the new amino acid based formula, a subgroup of child (n=15) will continue the second part of the study, with an open-label feeding with amino acid based formula for 180 days.
Time Frame
after 180 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
36 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Consecutive patients aged 1-36 months with diagnosis of Immunoglobulin E-mediated cow milk allergy in the last 12 weeks, full and stable remission of allergy symptoms Written informed consent form collected by the parents. Exclusion Criteria: Infant aged <1 months and >36 months, breast fed infants, other food allergies, other allergic diseases, evidence of non-IgE-mediated CMA, history of severe anaphylactic reaction, eosinophilic disorders of the gastrointestinal tract, chronic systemic diseases, congenital cardiac defects, active tuberculosis, autoimmune diseases, immunodeficiency, chronic inflammatory bowel diseases, celiac disease, cystic fibrosis, metabolic diseases, malignancy, chronic pulmonary diseases, malformations of the gastrointestinal and/or respiratory tract, use of systemic antibiotics or anti-mycotic drugs during 4 weeks before study entry; investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements; participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study.
Facility Information:
Facility Name
Rita Nocerino
City
Portici
State/Province
Napoli
ZIP/Postal Code
80055
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
RITA NOCERINO
Phone
3476510977
Email
ritanocerino@alice.it

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34217356
Citation
Nocerino R, Di Scala C, Coppola S, Giglio V, Carucci L, Cosenza L, Voto L, Iannicelli AM, Luzzetti A, Berni Canani R. Tolerability of a new amino acid-based formula for children with IgE-mediated cow's milk allergy. Ital J Pediatr. 2021 Jul 3;47(1):151. doi: 10.1186/s13052-021-01096-3.
Results Reference
derived

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Tolerability of Hypoallergenic Formula in Children With Cow's Milk Allergy

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