Impact of Infant Formula on Resolution of Cow's Milk Allergy

NCT ID: NCT02719405

Last Updated: 2018-07-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE2

Total Enrollment

49 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-29

Study Completion Date

2018-02-28

Brief Summary

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Primary Endpoint

-The percentage of subjects who develop tolerance to cow's milk protein by 12 months post randomization to study formula.

Secondary Endpoints

* Tolerance

* The transcriptional profile of milk-specific T cells by clinical outcome.
* Growth and Weight Velocity
* Stool Consistency and Frequency
* The estimated frequency of milk-specific T cells by clinical outcome.
* The TCR diversity of milk-specific T cells by clinical outcome.
* The milk allergen component-specific IgE, IgG4 and IgA by clinical outcome.
* Safety

* The rate of reported adverse events by treatment group.

Detailed Description

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Cow's Milk Allergy (CMA) is prevalent and most often presents during infancy. Disease manifestations vary through a range of immediate and delayed inflammatory responses to milk protein from anaphylaxis to enterocolitis. The natural history is also highly variable; most children will achieve clinical tolerance early in life, while a minority will have disease persisting to adulthood for reasons that are not known. Most presentations are mild and are managed by restriction or reduction of immunologically intact milk protein with reintroduction sometime after a year of age; however, there are data to suggest that some level of antigenic stimulation may be beneficial. Furthermore, recent data suggest that oral probiotic exposure may also promote tolerance, though the kinetics of tolerance acquisition, the interaction between these two factors (probiotics and milk antigen exposure) and their relationship to regulatory T cell responses are all poorly defined. Therefore, there is an unmet need to identify dietary interventions, along with corresponding immune responses, that favor the promotion of tolerance.

A major objective will be to measure the effect probiotics have on the development of tolerance to milk antigen over time. By following these infants during the first year of life, and repeatedly collecting blood and stool samples from them, we will be poised to analyze their stool microbiome signatures, and we will estimate the frequency, phenotype and TCR diversity of milk-specific T cells over time. By repeatedly challenging them with more immunologically intact milk protein, we will better define the kinetics of CMA resolution and its association to these variables. This information is likely to further elucidate CMA disease mechanisms and identify possible biomarkers of disease resolution versus persistence. It will be directly useful for evaluating the efficacy of probiotics and hydrolyzed formula for promoting milk tolerance.

Conditions

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Milk Allergy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Amino Acid Formula

Group Type PLACEBO_COMPARATOR

Amino Acid Formula

Intervention Type DIETARY_SUPPLEMENT

Amino Acid Formula

EHCF

Extensively Hydrolyzed Casein Formula

Group Type ACTIVE_COMPARATOR

Extensively Hydrolyzed Casein Formula

Intervention Type DIETARY_SUPPLEMENT

Extensively Hydrolyzed Casein Formula

EHCF + LGG

Extensively Hydrolyzed Casein Formula + Lactobacillus GG

Group Type ACTIVE_COMPARATOR

Lactobacillus GG

Intervention Type DIETARY_SUPPLEMENT

Lactobacillus GG

Extensively Hydrolyzed Casein Formula

Intervention Type DIETARY_SUPPLEMENT

Extensively Hydrolyzed Casein Formula

Interventions

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Lactobacillus GG

Lactobacillus GG

Intervention Type DIETARY_SUPPLEMENT

Extensively Hydrolyzed Casein Formula

Extensively Hydrolyzed Casein Formula

Intervention Type DIETARY_SUPPLEMENT

Amino Acid Formula

Amino Acid Formula

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Infants 0-120 days of age with suspected CMA, as determined by the pediatrician or specialist, will be referred to the study. A Standard Operating Procedures (SOP) document will be provided for the clinicians to help guide their referral to the study. Physician diagnosis of CMA will be based on the following:
* Physician documented, gross or persistent microscopic blood in stool (3 positive guaiac cards on three separate stools) in the absence of other explanation (e.g., fissure, moderate-to-severe constipation) AND / OR

Infant with at least one gastrointestinal, dermatological, or respiratory allergic manifestation suggestive of CMA:

* Gastrointestinal: Chronic Diarrhea, Constipation or Vomiting/Gastro-esophageal reflux
* Dermatologic: Atopic Dermatitis or Urticaria
* Respiratory: Cough, Allergic rhinitis or Recurrent Wheezing
* General:Colic / Irritability
* No change in treatment with medications during the 7 days preceding the elimination diet and no expected change in medications during the DBPCFCs (unless otherwise medically necessary)
* Signed informed consent obtained for infants participation in the study
* Signed authorization obtained to use and/or disclose Protected Health Information for infant from birth through the length of the study period

1. Caregiver(s) agree to comply with the infant elimination diet given to them by the investigator for the duration of the study
2. Mother agrees to follow an elimination diet throughout duration of breast feeding
3. Parent(s) or legally authorized representative agrees not to enroll infant in another interventional clinical study while participating in this study


* Positive Double Blind Placebo Controlled Food Challenge (DBPCFC).

Exclusion Criteria

* History of anaphylaxis to milk
* Use of probiotics
* Use in the previous 4 weeks of systemic steroids
* Use of systemic immunomodulatory treatment, including biologics with an immune target such as Xolair
* Known eosinophilic GI disorders
* Episode(s) of severe repetitive vomiting and lethargy prompting an emergency room visit and occurring within 4 hours of ingesting a milk protein (i.e. consistent with FPIES)
* Co-existing autoimmune or other chronic disease or serious health problem, including celiac disease, inflammatory bowel disease, malignancy, congenital, metabolic or genetic disorders or malformations
* Intention to exclusively breast feed
* Infants born at less than 36 weeks gestation (35 weeks + 6 days is considered 35 weeks gestation)


* Severe reaction to Milk Protein during the DBPCFC
Maximum Eligible Age

120 Days

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mead Johnson Nutrition

INDUSTRY

Sponsor Role collaborator

Massachusetts General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Wayne G. Shreffler, MD, PhD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Wayne G Shreffler, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

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Massachusetts General Hospital

Boston, Massachusetts, United States

Site Status

Woburn Pediatric Associates

Woburn, Massachusetts, United States

Site Status

Countries

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United States

References

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Amari S, Shahrook S, Namba F, Ota E, Mori R. Branched-chain amino acid supplementation for improving growth and development in term and preterm neonates. Cochrane Database Syst Rev. 2020 Oct 2;10(10):CD012273. doi: 10.1002/14651858.CD012273.pub2.

Reference Type DERIVED
PMID: 33006765 (View on PubMed)

Other Identifiers

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2015P000962

Identifier Type: -

Identifier Source: org_study_id

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