Impact of Infant Formula on Resolution of Cow's Milk Allergy
NCT ID: NCT02719405
Last Updated: 2018-07-13
Study Results
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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TERMINATED
PHASE2
49 participants
INTERVENTIONAL
2016-02-29
2018-02-28
Brief Summary
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-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.
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Detailed Description
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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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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
TRIPLE
Study Groups
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Amino Acid Formula
Amino Acid Formula
Amino Acid Formula
EHCF
Extensively Hydrolyzed Casein Formula
Extensively Hydrolyzed Casein Formula
Extensively Hydrolyzed Casein Formula
EHCF + LGG
Extensively Hydrolyzed Casein Formula + Lactobacillus GG
Lactobacillus GG
Lactobacillus GG
Extensively Hydrolyzed Casein Formula
Extensively Hydrolyzed Casein Formula
Interventions
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Lactobacillus GG
Lactobacillus GG
Extensively Hydrolyzed Casein Formula
Extensively Hydrolyzed Casein Formula
Amino Acid Formula
Amino Acid Formula
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
120 Days
ALL
No
Sponsors
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Mead Johnson Nutrition
INDUSTRY
Massachusetts General Hospital
OTHER
Responsible Party
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Wayne G. Shreffler, MD, PhD
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
Woburn Pediatric Associates
Woburn, Massachusetts, United States
Countries
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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.
Other Identifiers
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2015P000962
Identifier Type: -
Identifier Source: org_study_id
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