Icahn School of Medicine at Mount Sinai
New York, 10029, United States
NCT Number: NCT03907397
The primary objective of this study is to determine whether allowing ingestion of sub-threshold amounts of peanut in those with a high threshold (tolerate at least 143 mg peanut protein on supervised double-blind, placebo-controlled oral food challenge [DBPCFC]) will be associated with attaining even higher thresholds over time in children with high threshold peanut allergy compared to those avoiding peanut. The secondary clinical objectives include assessing the development of sustained unresponsiveness (SU, a surrogate term for tolerance without daily ingestion), effects on quality of life, and safety compared to those avoiding peanut. Additionally, this study will phenotype the allergic response to peanut based on threshold and response to exposure. Mechanistic study objectives will determine the immune and molecular basis of the high threshold endotype, identify predictors of response to exposure, and determine mechanisms and biomarkers of remission.
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Notify Me4 year–14 year
All sexes
Interventional
Phase 2
New York, 10029, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-Subject and/or parent guardian must be able to understand and provide informed consent.
Inclusion criteria
for screening DBPCFC:
Inclusion criteria
for randomization:
Exclusion criteria
Individuals who meet any of these criteria are not eligible for enrollment as study participants:
*Any subject meeting these criteria during the visits can be rescheduled for the oral food challenge or prick skin testing.*
up to 3 level teaspoons peanut butter or equivalent (approximately 3400 mg)
Standard of care avoidance of peanut
Time frame: 72 weeks
The difference between the treatment and comparison (avoidance) groups in the percentage of children who by the endpoint double-blind, placebo-controlled oral food challenge (DBPCFC) tolerate a dose at least 2 steps higher than their baseline DBPCFC or 9043 mg of peanut protein.
Due to missing data in the primary endpoint, the protocol & SAP specified a priori that missing data would be imputed using multiple imputation and results based on 30 completed-imputed data sets would be combined using Rubin's rule. In the Peanut Protein group, the observed data was so strong that participants with missing data were also imputed as success across all imputations (hence, 100% success rate). In the Peanut Avoidance group, there was more variability in the proportion of successes across imputations and these varying proportions were averaged. Missing data were imputed and results were pooled.
Time frame: 96 weeks
The percentage of children who achieve sustained unresponsiveness or natural tolerance during the study.
Time frame: 96 weeks
Safety parameter assessed by number of participants with acute allergic reactions which includes anaphylaxis or gastrointestinal side effects.
Time frame: baseline and at 72 weeks
The Food Allergy Quality of Life-Parental Burden (FAQL-PB) Scale is a 17-item instrument. It utilizes a 7-point Likert scale ranging from 0 (not troubled) to 6 (extremely troubled). The number circled for each question is summed to provide a total continuous score range of 0 to 102 with a higher score indicating greater burden on the family.
Time frame: Baseline and 72 weeks
Change in Skin Prick Test (SPT) mean wheal size at 72 weeks as compared to baseline. A skin test reaction is considered positive if the wheal size for the antigen is at least 3 mm larger than the wheal size of the negative control (saline).
Time frame: Baseline and 72 weeks
Mean Change in Peanut-specific IgE level at week 72 as compared to baseline.
Time frame: Baseline and 72 weeks
Mean Change in Peanut-specific IgG4 level at week 72 as compared to baseline.
Scott Sicherer
Other
Challenging to Food With Escalating Thresholds for Reducing Food Allergy
Acronym: CAFETERIA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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