Efficacy and safety of peanut epicutaneous immunotherapy in patients with atopic comorbidities.

Epicutaneous immunotherapy Viaskin Peanut children concomitant atopic conditions desensitization food allergy immunotherapy peanut allergy

Journal

The journal of allergy and clinical immunology. Global
ISSN: 2772-8293
Titre abrégé: J Allergy Clin Immunol Glob
Pays: United States
ID NLM: 9918453488706676

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 10 03 2022
revised: 11 07 2022
accepted: 18 07 2022
medline: 2 10 2023
pubmed: 2 10 2023
entrez: 2 10 2023
Statut: epublish

Résumé

Co-occurring atopic conditions are common in children with peanut allergy. As such, it is important to examine the safety and efficacy of epicutaneous immunotherapy with Viaskin Peanut 250 μg patch (VP250) in peanut-allergic children with these conditions. We sought to compare efficacy and safety of VP250 versus placebo in peanut-allergic children with/without ongoing atopic conditions at baseline, including asthma, atopic dermatitis/eczema, or concomitant food allergy. A subgroup analysis of peanut-allergic children aged 4 to 11 years enrolled in PEPITES (12 months) and REALISE (6 months) randomized, placebo-controlled, phase 3 trials was conducted. The efficacy outcome measure was the difference in prespecified responder rate between placebo and VP250 groups at month 12 based on eliciting dose of peanut protein using double-blind, placebo-controlled food challenge in PEPITES. Safety profiles were evaluated by baseline concomitant disease subgroup in all randomized subjects who received 1 or more dose of the study drug in PEPITES and REALISE pooled data. Responder rates were significantly ( The results support the safety and efficacy of VP250 for treating peanut-allergic children with or without concomitant atopic conditions.

Sections du résumé

Background UNASSIGNED
Co-occurring atopic conditions are common in children with peanut allergy. As such, it is important to examine the safety and efficacy of epicutaneous immunotherapy with Viaskin Peanut 250 μg patch (VP250) in peanut-allergic children with these conditions.
Objective UNASSIGNED
We sought to compare efficacy and safety of VP250 versus placebo in peanut-allergic children with/without ongoing atopic conditions at baseline, including asthma, atopic dermatitis/eczema, or concomitant food allergy.
Methods UNASSIGNED
A subgroup analysis of peanut-allergic children aged 4 to 11 years enrolled in PEPITES (12 months) and REALISE (6 months) randomized, placebo-controlled, phase 3 trials was conducted. The efficacy outcome measure was the difference in prespecified responder rate between placebo and VP250 groups at month 12 based on eliciting dose of peanut protein using double-blind, placebo-controlled food challenge in PEPITES. Safety profiles were evaluated by baseline concomitant disease subgroup in all randomized subjects who received 1 or more dose of the study drug in PEPITES and REALISE pooled data.
Results UNASSIGNED
Responder rates were significantly (
Conclusions UNASSIGNED
The results support the safety and efficacy of VP250 for treating peanut-allergic children with or without concomitant atopic conditions.

Identifiants

pubmed: 37780103
doi: 10.1016/j.jacig.2022.07.009
pii: S2772-8293(22)00071-6
pmc: PMC10509968
doi:

Types de publication

Journal Article

Langues

eng

Pagination

69-75

Informations de copyright

© 2022 The Authors.

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Auteurs

Carla M Davis (CM)

Department of Pediatrics, Immunology, Allergy and Retrovirology Section, Baylor College of Medicine, Houston, Tex.

Lars Lange (L)

Department of Pediatrics, St. Marien Hospital Bonn, Bonn, Germany.

Kirsten Beyer (K)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitatsmedizin Berlin, Berlin, Germany.

David M Fleischer (DM)

Children's Hospital Colorado, University of Colorado Denver School of Medicine, Aurora, Colo.

Lara Ford (L)

Department of Allergy and Immunology, The Children's Hospital at Westmead, Sydney, Australia.
Discipline of Child and Adolescent Health, University of Sydney School of Medicine, Sydney, Australia.

Gordon Sussman (G)

Division of Clinical Immunology and Allergy, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Gordon Sussman Clinical Research, Toronto, Ontario, Canada.

Roxanne C Oriel (RC)

Department of Pediatrics, Division of Allergy & Immunology, Icahn School of Medicine at Mount Sinai, New York, NY.

Jacqueline A Pongracic (JA)

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill.

Wayne Shreffler (W)

Food Allergy Center, Departments of Pediatrics and Medicine, Massachusetts General Hospital, Boston, Mass.

Katharine J Bee (KJ)

DBV Technologies SA, Montrouge, France.

Dianne E Campbell (DE)

DBV Technologies SA, Montrouge, France.

Todd D Green (TD)

DBV Technologies SA, Montrouge, France.
UPMC Children's Hospital of Pittsburgh and University of Pittsburgh School of Medicine, Pittsburgh, Pa.

Romain Lambert (R)

DBV Technologies SA, Montrouge, France.

Aurélie Peillon (A)

DBV Technologies SA, Montrouge, France.

Philippe Bégin (P)

Oral Immunotherapy Clinic, CHU Sainte-Justine, Montreal, Quebec, Canada.

Classifications MeSH