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Extensively Hydrolyzed Infant Formula in Infants and Children With Cow's Milk Allergy

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Abbott

Status

Terminated

Conditions

Cow's Milk Allergy

Treatments

Other: Placebo Extensively Hydrolyzed Formula
Other: Experimental Extensively Hydrolyzed Formula

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

This is a multi-center, randomized, double-blind, placebo-controlled food challenge to be conducted in infants or children with confirmed IgE-mediated cow's milk allergy (CMA), followed by a 7-day open feeding of the experimental formula.

Enrollment

1 patient

Sex

All

Ages

3 months to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participant has a physician diagnosis of IgE-mediated Cow's Milk Allergy (CMA) based on a clinical history of a reaction resulting in characteristic immediate hypersensitivity symptoms within 2 hours of oral exposure or immediate hypersensitivity symptoms according to physician's observation

  • Participant is willing to undergo confirmatory testing or must have had at least one of the following within 6 months of enrollment:

    1. Documentation of milk-specific serum IgE >15 kIUA/L or > 5 kIUA/L if younger than 1 year.
    2. Documented cow's milk skin prick test mean wheal >10mm
    3. Physician-supervised oral food challenge that elicited immediate, objective, allergic symptoms.
  • Participant agrees to stop oral steroid use within 14 days and antihistamine use within 7 days of confirmation of diagnosis and food challenges.

  • Participant had followed a strict cow's milk protein-free diet prior to enrollment.

  • Parent(s) confirm their intention not to administer any products containing cow's milk protein during the study.

  • Participant's parent(s) has voluntarily signed and dated an Informed Consent Form (ICF), approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) and provided Health Insurance Portability and Accountability Act (HIPAA) (or other applicable privacy regulation) authorization prior to any participation in the study.

Exclusion criteria

  • Participant is exclusively breastfed at the time of enrollment.
  • Participant is consuming an amino acid-based formula due to failure on an extensively hydrolyzed formula.
  • Significant chronic medical diseases including major chromosomal or congenital anomalies, gastrointestinal diseases or abnormalities other than CMA, immunodeficiencies, unstable asthma, asthma treated with biologics (omalizumab or other monoclonal antibody), FPIES, eosinophilic esophagitis, and severe uncontrolled eczema.
  • Previous severe anaphylactic reaction to cow's milk within the last two years.
  • An adverse medical history or current condition that is thought by the investigator to have potential for effects on tolerance or the hypoallergenicity test.
  • Participant has an allergy or intolerance to any ingredient in the study product, as reported by the parent.
  • Participant is routinely consuming baked milk products.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

1 participants in 2 patient groups, including a placebo group

Experimental Extensively Hydrolyzed Formula
Experimental group
Description:
Administered during food challenge and at home feeding period
Treatment:
Other: Experimental Extensively Hydrolyzed Formula
Placebo Extensively Hydrolyzed Formula
Placebo Comparator group
Description:
Administered during food challenge
Treatment:
Other: Placebo Extensively Hydrolyzed Formula

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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