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Oral Immunotherapy for Peanut Allergy in Children 1 to Less Than 4 Years of Age.

Authors :
Du Toit, George
Brown, Kari R.
Vereda, Andrea
Irani, Anne-Marie
Tilles, Stephen
Ratnayake, Anoshie
Jones, Stacie M.
Vickery, Brian P.
Source :
NEJM Evidence; Nov2023, Vol. 2 Issue 11, p9-9, 1p
Publication Year :
2023

Abstract

Background Peanut allergy is a common childhood allergy, and the only approved treatment for children 4 to 17 years of age is peanut allergen powder-dnfp (PTAH) oral immunotherapy. Methods For this phase 3, randomized, double-blind, placebo-controlled trial, we enrolled peanut-allergic children 1 to >4 years of age who experienced dose-limiting symptoms from ≤300 mg peanut protein during a screening double-blind, placebo-controlled food challenge (DBPCFC). Participants received PTAH or placebo, randomized in a 2:1 ratio, for approximately 12 months. At the trial conclusion, all participants underwent an exit BDPCFC. The primary end point was desensitization (i.e., tolerating a ≥600-mg single dose of peanut protein with only mild allergy symptoms). Results In the PTAH-treated group (n=98), 73.5% of participants tolerated a single dose of ≥600 mg peanut protein at exit DBPCFC compared with 6.3% in the placebo group (n=48). Most participants experienced an adverse event (98.0% of PTAH-treated and 97.9% of placebo-treated participants), which was mild or moderate in grade for 93.2% of participants (92.9% in PTAH-treated and 93.8% in placebo-treated participants). Treatment-related adverse events, which were mild to moderate, were experienced by 75.5% of PTAH-treated and 58.3% of placebo-treated participants. Three treatment-related systemic allergic reactions, none of which were severe or serious in grade, were noted in two PTAH-treated participants (2%). Conclusions In peanut-allergic children 1 to >4 years of age treated with PTAH for approximately 12 months, the majority tolerated all peanut protein dose levels assessed. PTAH-treated patients had more treatment-related adverse events, which were mild to moderate severity. (Funded by Aimmune Therapeutics; ClinicalTrials.gov number, NCT03736447.) [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
27665526
Volume :
2
Issue :
11
Database :
Supplemental Index
Journal :
NEJM Evidence
Publication Type :
Academic Journal
Accession number :
173383258
Full Text :
https://doi.org/10.1056/EVIDoa2300145