A Randomized Controlled Trial of Oral Immunotherapy Versus Allergen Avoidance in Children Under 2 Years With Food Allergy (SAFARI)
A Systems Biology Approach to Treatment of Food Allergy: A Randomized Controlled Trial of Oral Immunotherapy in Children Under 2 Years (SAFARI)
The goal of this clinical trial is to learn whether oral immunotherapy (OIT) is safe and effective for treating food allergy in children aged 0-2 years with peanut, tree nut, or sesame allergy. The study also aims to identify biological mechanisms and biomarkers associated with natural tolerance development and successful OIT using a systems biology approach.
The main questions it aims to answer are:
- Does oral immunotherapy increase the likelihood of successful desensitization and sustained unresponsiveness compared with allergen avoidance?
- Can immune, microbiome, metabolomic, genetic, and epigenetic profiles predict treatment response, natural tolerance development, and long-term outcomes?
Researchers will compare children receiving oral immunotherapy with children receiving standard care (allergen avoidance) to determine differences in treatment success, sustained unresponsiveness, safety, quality of life, and biological markers.
Participants will:
- Be randomized to either oral immunotherapy or allergen avoidance for 18-24 months.
- Undergo oral food challenges at study visits to assess allergic reactivity and treatment outcomes.
- Provide blood, urine, hair, skin swabs, skin tape strips, throat swabs, nasal lining fluid, and stool samples at baseline and at the end of the study for immune, microbiome, metabolomic, gene expression, and epigenetic analyses.
- Complete allergy assessments, including skin prick testing and clinical evaluations.
- Have allergic symptoms, adverse reactions, and development of other allergic diseases monitored throughout the study.
- Have parents complete questionnaires assessing food allergy-related quality of life, anxiety, and coping.
調査の概要
詳細な説明
Food allergy affects approximately 4% of children worldwide and has increased over the past two decades, imposing substantial psychosocial and economic burden on affected families. For years, management relied on strict avoidance of the allergen and carrying an epinephrine autoinjector, which leads to tolerance development among 10-30% with peanut, tree-nut and sesame allergy. Treatments for food allergy such as biologics and oral immunotherapy (OIT) have shown a promising safety and efficacy profile in most studies, especially in younger children, but are not yet standard of care.
Biologics, including monoclonal antibodies targeting IgE (such as omalizumab) or key type 2 inflammatory pathways (e.g. dupilumab), offer an emerging strategy for managing food allergy. Used as stand-alone therapy, biologics can raise the threshold for allergic reactions and reduce symptom severity. Moreover, biologics have also been studied as adjuncts to OIT, where they may improve safety profiles, reduce dosing-related reactions, and facilitate more rapid desensitization. However, trials in young children assessing both safety, efficacy, mechanism and potential biomarkers are needed to inform personalized strategies, determining which children might benefit most from an avoidance strategy, OIT alone, biologics alone, or a combined approach. Currently, Palforzia is the only European Medicines Agency (EMA) approved OIT product available and approved for children from 4-17 years of age, whereas there are no OIT treatment options for the youngest children, where the prevalence of food allergy is highest.
Peanut OIT is gaining support based on real-world evidence, but OIT RCTs in young children under age 6 years are scarce and limited to studies of peanut and egg. The short term desensitization rates following peanut OIT range from 60% to 85%, and are higher when treatment begins in preschool age. Gastrointestinal and respiratory symptoms are common during peanut OIT, whereas rates of anaphylaxis requiring epinephrine are varying but relatively low, where up to 14% has been reported. Data for tree-nut OIT, e.g., hazelnut, cashew, pistachio, walnut and almond, is limited to a single-center retrospective study on hazelnut OIT in children < 18 years, and a single-center prospective cohort study on walnut OIT in children from 4-20 years. Further, data on tree-nut allergy has been extrapolated from an omalizumab-supported multifood OIT study in children from 4-15 years, which included cashew, walnut, hazelnut, and almond. Although outcomes and study design varied considerably, short term desensitization following tree-nut OIT ranged from 34% to 100%. Analysis of preliminary safety data is promising, with primarily mild reactions comparable with peanut OIT. Evidence for sesame OIT is very limited and solely based on small observational cohorts, case series, or extrapolated from multifood OIT protocols including sesame. Reported short term desensitization rates vary from 55% to 80%, and the majority of adverse reactions are mild.
Thus, while short term safety and efficacy of peanut, tree-nut, and sesame OIT seems promising, RCTs are needed in the youngest children, where food allergy is most prevalent. Moreover, although short term desensitization rates are encouraging, long term tolerance to the food - known as sustained unresponsiveness after discontinuing OIT - has proven more elusive. Follow-up studies show that many children relapse once therapy ends. Thus, there is a need for studies to identify underlying mechanisms and biomarkers predicting sustained unresponsiveness versus relapse, i.e. personalized treatment. In addition, some children will outgrow their food allergy during avoidance, i.e., natural tolerance development, but the mechanisms underlying natural tolerance are poorly understood, and no reliable predictors exist. Further, open-label quality-of-life (QoL) studies have consistently shown that OIT substantially reduces family anxiety concerning accidental exposures and improves daily functioning, but this still needs to be investigated in the youngest children in RCTs with a proper comparison of children undergoing avoidance vs. OIT. Finally, no previous study has investigated facilitators and barriers for implementing OIT in clinical practice, despite its higher resource demands and higher risk of adverse reactions compared to standard of care.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Bo Chawes
- 電話番号:+4538681152
- メール:chawes@copsac.com
研究場所
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Capital Region
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Herlev、Capital Region、デンマーク、2730
- Department of Paediatrics, Herlev Hospital
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参加基準
適格基準
就学可能な年齢
- 子
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Children age 0-2 years
- Diagnosed IgE-mediated food allergy to tree-nuts, sesame, and/or peanuts, defined as: Positive oral food challenge (OFC) at inclusion or within 6 months before AND positive SPT (≥ 3 mm) or specific IgE (≥ 0.35 kUA/L)
- Both parents provide informed consent
Exclusion Criteria:
- Already undergoing any form of immunotherapy
- Already undergoing any form of biological treatment
- Medical conditions precluding OITs: Uncontrolled asthma, atopic dermatitis requiring systemic therapy, eosinophilic esophagitis (EoE) and other GI-diseases, other severe immunological diseases (e.g. inborn errors of immunity )
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:Intervention arm
Participants will receive oral immunotherapy (OIT) for their diagnosed food allergy to peanut, tree nuts, or sesame.
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Daily OIT will be administered with the relevant food allergen. Treatment includes gradual dose escalation over approximately 6 months, followed by a 12-month maintenance phase with daily intake of 300 mg food protein. Assessment of sustained unresponsiveness: Following completion of OIT and a successful end-of-treatment oral food challenge, participants in the OIT arm will undergo a second 1:1 randomization to either continued regular allergen consumption or allergen avoidance. After an additional 6 months, participants will undergo another oral food challenge to assess sustained unresponsiveness. |
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介入なし:Control arm
Participants randomized to the control arm will follow standard of care consisting of avoidance of the relevant food allergen.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Oral Food Challenge Response at End of Treatment
時間枠:End of treatment, approximately 18-24 months after randomization
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Effect of oral immunotherapy will be assessed by oral food challenge (OFC) at the end of treatment and compared with the control arm.
Participants will be classified into predefined response categories: successful responders, defined as participants tolerating a 4000 mg food protein OFC; partial responders, defined as participants with an increased reaction threshold to at least 1000 mg food protein but not tolerating the final 4000 mg OFC and/or experiencing difficulties during up-dosing; and non-responders, defined as participants discontinuing OIT due to allergic reactions or having a reaction threshold below 1000 mg food protein.
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End of treatment, approximately 18-24 months after randomization
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Difficulty With Up-dosing During Oral Immunotherapy
時間枠:During the up-dosing phase, approximately 0-6 months after treatment initiation.
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Difficulty with up-dosing will be assessed in participants randomized to the OIT group.
Difficulty is defined as allergic reactions, dose reductions, delayed dose escalation, temporary treatment interruption, or inability to complete the planned up-dosing phase according to protocol.
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During the up-dosing phase, approximately 0-6 months after treatment initiation.
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Sustained Unresponsiveness
時間枠:24-30 months after initial randomization, corresponding to approximately 6 months after completion of OIT.
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Sustained unresponsiveness will be assessed by oral food challenge (OFC) after 6 months of either avoidance or regular intake of the allergenic food, according to randomization after completion of OIT.
Success of the OFC will indicate potential long-term tolerance rather than transient desensitization.
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24-30 months after initial randomization, corresponding to approximately 6 months after completion of OIT.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Change in Gut Microbiome Diversity Assessed by Shannon Index
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Change from baseline to end of treatment in gut microbiome diversity, assessed using the Shannon Index based on shotgun metagenomic sequencing of stool samples.
Changes over time will be assessed within treatment groups and compared between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in Fecal Metabolite Levels
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes from baseline to end of treatment in fecal metabolite levels will be assessed using untargeted metabolomic profiling of stool samples.
Changes in metabolite levels over time will be assessed within treatment groups, and differences in these changes will be compared between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in Blood Immunoglobulin Markers
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes from baseline to end of treatment in blood immunoglobulin markers, including food-specific IgG1 and IgG4 and total IgE, will be assessed.
Changes over time will be assessed within treatment groups and compared between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in Mast Cell Activation
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Change from baseline to end of treatment in mast cell activation in response to peanut, sesame, and tree nuts will be assessed using the Mast Cell Activation Test (MAT).
Changes over time will be assessed within treatment groups and compared between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in Plasma Metabolite Levels
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes from baseline to end of treatment in plasma metabolite levels will be assessed by metabolomic profiling using Liquid Chromatography-Mass Spectrometry (LC-MS) and Gas Chromatography-Mass Spectrometry (GC-MS) using the Global HD4 platform at Metabolon Inc., US. Changes in metabolite levels over time will be assessed within treatment groups, and differences in these changes will be compared between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Rate and Severity of Allergic Reactions During Oral Immunotherapy
時間枠:From initiation of OIT to end of treatment, approximately 18-24 months after randomization.
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The number and severity of anaphylaxis and other allergic reactions during OIT will be recorded at build-up visits and maintenance follow-up visits, including symptoms since the last visit, missed doses, accidental exposures, relevant cofactors, and treatments required.
Reactions will be graded according to a modified World Allergy Organization grading system, grades 1 to 5, with adaptations specific to allergic reactions in infants.
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From initiation of OIT to end of treatment, approximately 18-24 months after randomization.
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Change in Parental Food Allergy-associated Anxiety and Coping
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes in parental food allergy-associated anxiety, coping, and impact on daily life will be assessed using the Impairment Measure for Parental Food Allergy-Associated Anxiety and Coping Tool (IMPAACT).
The questionnaire will be completed by parents at baseline and at the end of the randomized controlled trial, and changes will be assessed within and between treatment groups.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in Allergic Sensitization
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes in allergic sensitization to the relevant food allergen will be assessed by specific IgE and skin prick testing.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Development of New Allergic Sensitizations and Atopic Manifestations
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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The development of new food or inhalant sensitizations and new atopic manifestations will be assessed and compared between treatment groups.
Atopic manifestations may include wheeze, allergic rhinitis, and atopic dermatitis.
Atopic dermatitis will be assessed using established diagnostic criteria and severity scoring.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Prediction of Sustained Unresponsiveness
時間枠:Baseline to assessment of sustained unresponsiveness, approximately 24-30 months after randomization.
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Different omics layers will be used to explore whether sustained unresponsiveness can be predicted.
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Baseline to assessment of sustained unresponsiveness, approximately 24-30 months after randomization.
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Change in PBMC Gene Expression Profiles
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes from baseline to end of treatment in gene expression profiles will be assessed in peripheral blood mononuclear cells (PBMCs).
Changes in gene expression over time will be assessed within treatment groups and compared between treatment groups and may additionally be evaluated as part of exploratory multivariate and multi-omics analyses.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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Change in PBMC Epigenetic Profiles
時間枠:Baseline to end of treatment, approximately 18-24 months after randomization.
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Changes from baseline to end of treatment in epigenetic profiles will be assessed in peripheral blood mononuclear cells (PBMCs).
Changes in epigenetic markers over time will be assessed within treatment groups and compared between treatment groups and may additionally be evaluated as part of exploratory multivariate and multi-omics analyses.
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Baseline to end of treatment, approximately 18-24 months after randomization.
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協力者と研究者
出版物と役立つリンク
一般刊行物
- DunnGalvin A, Dubois AE, Flokstra-de Blok BM, Hourihane JO. The effects of food allergy on quality of life. Chem Immunol Allergy. 2015;101:235-52. doi: 10.1159/000375106. Epub 2015 May 21.
- Leung DY, Sampson HA, Yunginger JW, Burks AW Jr, Schneider LC, Wortel CH, Davis FM, Hyun JD, Shanahan WR Jr; Avon Longitudinal Study of Parents and Children Study Team. Effect of anti-IgE therapy in patients with peanut allergy. N Engl J Med. 2003 Mar 13;348(11):986-93. doi: 10.1056/NEJMoa022613. Epub 2003 Mar 10.
- Nachshon L, Goldberg MR, Levy MB, Appel MY, Epstein-Rigbi N, Lidholm J, Holmqvist M, Katz Y, Elizur A. Efficacy and Safety of Sesame Oral Immunotherapy-A Real-World, Single-Center Study. J Allergy Clin Immunol Pract. 2019 Nov-Dec;7(8):2775-2781.e2. doi: 10.1016/j.jaip.2019.05.031. Epub 2019 May 29.
- PALISADE Group of Clinical Investigators; Vickery BP, Vereda A, Casale TB, Beyer K, du Toit G, Hourihane JO, Jones SM, Shreffler WG, Marcantonio A, Zawadzki R, Sher L, Carr WW, Fineman S, Greos L, Rachid R, Ibanez MD, Tilles S, Assa'ad AH, Nilsson C, Rupp N, Welch MJ, Sussman G, Chinthrajah S, Blumchen K, Sher E, Spergel JM, Leickly FE, Zielen S, Wang J, Sanders GM, Wood RA, Cheema A, Bindslev-Jensen C, Leonard S, Kachru R, Johnston DT, Hampel FC Jr, Kim EH, Anagnostou A, Pongracic JA, Ben-Shoshan M, Sharma HP, Stillerman A, Windom HH, Yang WH, Muraro A, Zubeldia JM, Sharma V, Dorsey MJ, Chong HJ, Ohayon J, Bird JA, Carr TF, Siri D, Fernandez-Rivas M, Jeong DK, Fleischer DM, Lieberman JA, Dubois AEJ, Tsoumani M, Ciaccio CE, Portnoy JM, Mansfield LE, Fritz SB, Lanser BJ, Matz J, Oude Elberink HNG, Varshney P, Dilly SG, Adelman DC, Burks AW. AR101 Oral Immunotherapy for Peanut Allergy. N Engl J Med. 2018 Nov 22;379(21):1991-2001. doi: 10.1056/NEJMoa1812856. Epub 2018 Nov 18.
- Gupta RS, Springston EE, Warrier MR, Smith B, Kumar R, Pongracic J, Holl JL. The prevalence, severity, and distribution of childhood food allergy in the United States. Pediatrics. 2011 Jul;128(1):e9-17. doi: 10.1542/peds.2011-0204. Epub 2011 Jun 20.
- Wood RA, Kim JS, Lindblad R, Nadeau K, Henning AK, Dawson P, Plaut M, Sampson HA. A randomized, double-blind, placebo-controlled study of omalizumab combined with oral immunotherapy for the treatment of cow's milk allergy. J Allergy Clin Immunol. 2016 Apr;137(4):1103-1110.e11. doi: 10.1016/j.jaci.2015.10.005. Epub 2015 Nov 12.
- Shah A, Cox AL, Groetch M, Kattan JD, Schaible A, Sicherer SH, Tsuang A, Wang J, Oriel RC. Sesame oral immunotherapy outcomes in a pediatric cohort. J Allergy Clin Immunol Pract. 2025 Apr;13(4):938-940.e1. doi: 10.1016/j.jaip.2025.01.036. Epub 2025 Feb 8. No abstract available.
- Jones SM, Kim EH, Nadeau KC, Nowak-Wegrzyn A, Wood RA, Sampson HA, Scurlock AM, Chinthrajah S, Wang J, Pesek RD, Sindher SB, Kulis M, Johnson J, Spain K, Babineau DC, Chin H, Laurienzo-Panza J, Yan R, Larson D, Qin T, Whitehouse D, Sever ML, Sanda S, Plaut M, Wheatley LM, Burks AW; Immune Tolerance Network. Efficacy and safety of oral immunotherapy in children aged 1-3 years with peanut allergy (the Immune Tolerance Network IMPACT trial): a randomised placebo-controlled study. Lancet. 2022 Jan 22;399(10322):359-371. doi: 10.1016/S0140-6736(21)02390-4.
- Erdle SC, Cook VE, Cameron SB, Yeung J, Kapur S, McHenry M, Chan ES, Mak R, Rex GA, Wong T, Soller L. Real-World Safety Analysis of Preschool Tree Nut Oral Immunotherapy. J Allergy Clin Immunol Pract. 2023 Apr;11(4):1177-1183. doi: 10.1016/j.jaip.2023.01.031. Epub 2023 Feb 1.
- Huang J, Puglisi LH, Cook KA, Kelso JM, Wangberg H. Safety and Feasibility of Peanut, Tree Nut, and Sesame Oral Immunotherapy in Infants and Toddlers in a Real-World Setting. J Allergy Clin Immunol Pract. 2025 Jan;13(1):185-191.e3. doi: 10.1016/j.jaip.2024.09.025. Epub 2024 Sep 30.
- Tang MLK, Lozinsky AC, Loke P. Peanut Oral Immunotherapy: State of the Art. Immunol Allergy Clin North Am. 2020 Feb;40(1):97-110. doi: 10.1016/j.iac.2019.09.005. Epub 2019 Nov 6.
- Blackman AC, Staggers KA, Kronisch L, Davis CM, Anagnostou A. Quality of life improves significantly after real-world oral immunotherapy for children with peanut allergy. Ann Allergy Asthma Immunol. 2020 Aug;125(2):196-201.e1. doi: 10.1016/j.anai.2020.03.028. Epub 2020 Apr 8.
- Epstein-Rigbi N, Goldberg MR, Levy MB, Nachshon L, Elizur A. Quality of Life of Food-Allergic Patients Before, During, and After Oral Immunotherapy. J Allergy Clin Immunol Pract. 2019 Feb;7(2):429-436.e2. doi: 10.1016/j.jaip.2018.06.016. Epub 2018 Jul 7.
- Chinthrajah RS, Purington N, Andorf S, Long A, O'Laughlin KL, Lyu SC, Manohar M, Boyd SD, Tibshirani R, Maecker H, Plaut M, Mukai K, Tsai M, Desai M, Galli SJ, Nadeau KC. Sustained outcomes in oral immunotherapy for peanut allergy (POISED study): a large, randomised, double-blind, placebo-controlled, phase 2 study. Lancet. 2019 Oct 19;394(10207):1437-1449. doi: 10.1016/S0140-6736(19)31793-3. Epub 2019 Sep 12.
- Keet CA, Seopaul S, Knorr S, Narisety S, Skripak J, Wood RA. Long-term follow-up of oral immunotherapy for cow's milk allergy. J Allergy Clin Immunol. 2013 Sep;132(3):737-739.e6. doi: 10.1016/j.jaci.2013.05.006. Epub 2013 Jun 25. No abstract available.
- Chua GT, Soller L, Kapur S, McHenry M, Rex GA, Cook VE, Cameron SB, Chan ES, Yeung J, Erdle SC. Real-world safety and effectiveness analysis of low-dose preschool sesame oral immunotherapy. J Allergy Clin Immunol Glob. 2023 Sep 23;3(1):100171. doi: 10.1016/j.jacig.2023.100171. eCollection 2024 Feb.
- Andorf S, Purington N, Block WM, Long AJ, Tupa D, Brittain E, Rudman Spergel A, Desai M, Galli SJ, Nadeau KC, Chinthrajah RS. Anti-IgE treatment with oral immunotherapy in multifood allergic participants: a double-blind, randomised, controlled trial. Lancet Gastroenterol Hepatol. 2018 Feb;3(2):85-94. doi: 10.1016/S2468-1253(17)30392-8. Epub 2017 Dec 12.
- Elizur A, Appel MY, Nachshon L, Levy MB, Epstein-Rigbi N, Pontoppidan B, Lidholm J, Goldberg MR. Walnut oral immunotherapy for desensitisation of walnut and additional tree nut allergies (Nut CRACKER): a single-centre, prospective cohort study. Lancet Child Adolesc Health. 2019 May;3(5):312-321. doi: 10.1016/S2352-4642(19)30029-X. Epub 2019 Mar 27.
- Moraly T, Pelletier de Chambure D, Verdun S, Preda C, Seynave M, Vilain AC, Chenivesse C, Delebarre-Sauvage C. Oral Immunotherapy for Hazelnut Allergy: A Single-Center Retrospective Study on 100 Patients. J Allergy Clin Immunol Pract. 2020 Feb;8(2):704-709.e4. doi: 10.1016/j.jaip.2019.10.045. Epub 2019 Nov 18.
- Soller L, Carr S, Kapur S, Rex GA, McHenry M, Cook VE, Leo S, Wong T, Vander Leek TK, Gerstner TV, Yeung J, Abrams EM, Mak R, Hildebrand KJ, Erdle SC, Cameron SB, Chan ES. Real-world peanut OIT in infants may be safer than non-infant preschool OIT and equally effective. J Allergy Clin Immunol Pract. 2022 Apr;10(4):1113-1116.e1. doi: 10.1016/j.jaip.2021.12.009. Epub 2021 Dec 23. No abstract available.
- Burks AW, Jones SM, Wood RA, Fleischer DM, Sicherer SH, Lindblad RW, Stablein D, Henning AK, Vickery BP, Liu AH, Scurlock AM, Shreffler WG, Plaut M, Sampson HA; Consortium of Food Allergy Research (CoFAR). Oral immunotherapy for treatment of egg allergy in children. N Engl J Med. 2012 Jul 19;367(3):233-43. doi: 10.1056/NEJMoa1200435.
- Lee ECK, Trogen B, Brady K, Ford LS, Wang J. The Natural History and Risk Factors for the Development of Food Allergies in Children and Adults. Curr Allergy Asthma Rep. 2024 Mar;24(3):121-131. doi: 10.1007/s11882-024-01131-3. Epub 2024 Feb 28.
- Borne GE, Daniel CP, Wagner MJ, Plaisance CJ, Nolen A, Kelkar RA, Ahmadzadeh S, Myrcik D, Shekoohi S, Kaye AD, Varrassi G. Palforzia for Peanut Allergy: A Narrative Review and Update on a Novel Immunotherapy. Cureus. 2023 Dec 13;15(12):e50485. doi: 10.7759/cureus.50485. eCollection 2023 Dec.
- Andorf S, Purington N, Kumar D, Long A, O'Laughlin KL, Sicherer S, Sampson H, Cianferoni A, Whitehorn TB, Petroni D, Makhija M, Robison RG, Lierl M, Logsdon S, Desai M, Galli SJ, Rael E, Assa'ad A, Chinthrajah S, Pongracic J, Spergel JM, Tam J, Tilles S, Wang J, Nadeau K. A Phase 2 Randomized Controlled Multisite Study Using Omalizumab-facilitated Rapid Desensitization to Test Continued vs Discontinued Dosing in Multifood Allergic Individuals. EClinicalMedicine. 2019 Jan 21;7:27-38. doi: 10.1016/j.eclinm.2018.12.006. eCollection 2019 Jan.
- Zuberbier T, Wood RA, Bindslev-Jensen C, Fiocchi A, Chinthrajah RS, Worm M, Deschildre A, Fernandez-Rivas M, Santos AF, Jaumont X, Tassinari P. Omalizumab in IgE-Mediated Food Allergy: A Systematic Review and Meta-Analysis. J Allergy Clin Immunol Pract. 2023 Apr;11(4):1134-1146. doi: 10.1016/j.jaip.2022.11.036. Epub 2022 Dec 15.
- Chinthrajah RS, Sindher SB, Nadeau KC, Leflein JG, Spergel JM, Petroni DH, Jones SM, Casale TB, Wang J, Carr WW, Shreffler WG, Wood RA, Wambre E, Liu J, Akinlade B, Atanasio A, Orengo JM, Hamilton JD, Kamal MA, Hooper AT, Patel K, Laws E, Mannent LP, Adelman DC, Ratnayake A, Radin AR. Dupilumab as an Adjunct to Oral Immunotherapy in Pediatric Patients With Peanut Allergy. Allergy. 2025 Mar;80(3):827-842. doi: 10.1111/all.16420. Epub 2024 Dec 14.
- Sindher SB, Fiocchi A, Zuberbier T, Arasi S, Wood RA, Chinthrajah RS. The Role of Biologics in the Treatment of Food Allergy. J Allergy Clin Immunol Pract. 2024 Mar;12(3):562-568. doi: 10.1016/j.jaip.2023.11.032. Epub 2023 Nov 25.
- Soller L, Abrams EM, Carr S, Kapur S, Rex GA, Leo S, Lidman PG, Yeung J, Vander Leek TK, McHenry M, Wong T, Cook VE, Hildebrand KJ, Gerstner TV, Mak R, Lee NJ, Cameron SB, Chan ES. First Real-World Safety Analysis of Preschool Peanut Oral Immunotherapy. J Allergy Clin Immunol Pract. 2019 Nov-Dec;7(8):2759-2767.e5. doi: 10.1016/j.jaip.2019.04.010. Epub 2019 Apr 17.
- Karunakaran D, Chan ES, Zhang Q, Bone JN, Carr S, Kapur S, Rex GA, McHenry M, Cameron SB, Cook VE, Leo S, Wong T, Gerstner TV, Yeung J, Abrams EM, Mak R, Erdle SC, Soller L. Risk factors associated with safety of preschool peanut oral immunotherapy. J Allergy Clin Immunol Glob. 2023 Mar 21;2(2):100094. doi: 10.1016/j.jacig.2023.100094. eCollection 2023 May.
- Wood RA, Togias A, Sicherer SH, Shreffler WG, Kim EH, Jones SM, Leung DYM, Vickery BP, Bird JA, Spergel JM, Iqbal A, Olsson J, Ligueros-Saylan M, Uddin A, Calatroni A, Huckabee CM, Rogers NH, Yovetich N, Dantzer J, Mudd K, Wang J, Groetch M, Pyle D, Keet CA, Kulis M, Sindher SB, Long A, Scurlock AM, Lanser BJ, Lee T, Parrish C, Brown-Whitehorn T, Spergel AKR, Veri M, Hamrah SD, Brittain E, Poyser J, Wheatley LM, Chinthrajah RS. Omalizumab for the Treatment of Multiple Food Allergies. N Engl J Med. 2024 Mar 7;390(10):889-899. doi: 10.1056/NEJMoa2312382. Epub 2024 Feb 25.
- Jeong K, Lee S. Natural course of IgE-mediated food allergy in children. Clin Exp Pediatr. 2023 Dec;66(12):504-511. doi: 10.3345/cep.2022.01004. Epub 2023 Jun 14.
- Golding MA, Batac ALR, Gunnarsson NV, Ahlstedt S, Middelveld R, Protudjer JLP. The burden of food allergy on children and teens: A systematic review. Pediatr Allergy Immunol. 2022 Mar;33(3):e13743. doi: 10.1111/pai.13743.
- Golding MA, Protudjer JLP. A review of food allergy-related costs with consideration to clinical and demographic factors. Curr Opin Allergy Clin Immunol. 2023 Jun 1;23(3):246-251. doi: 10.1097/ACI.0000000000000903. Epub 2023 Mar 28.
- Branum AM, Lukacs SL. Food allergy among children in the United States. Pediatrics. 2009 Dec;124(6):1549-55. doi: 10.1542/peds.2009-1210. Epub 2009 Nov 16.
- Boyce JA, Assa'ad A, Burks AW, Jones SM, Sampson HA, Wood RA, Plaut M, Cooper SF, Fenton MJ, Arshad SH, Bahna SL, Beck LA, Byrd-Bredbenner C, Camargo CA Jr, Eichenfield L, Furuta GT, Hanifin JM, Jones C, Kraft M, Levy BD, Lieberman P, Luccioli S, McCall KM, Schneider LC, Simon RA, Simons FE, Teach SJ, Yawn BP, Schwaninger JM; NIAID-Sponsored Expert Panel. Guidelines for the Diagnosis and Management of Food Allergy in the United States: Summary of the NIAID-Sponsored Expert Panel Report. J Allergy Clin Immunol. 2010 Dec;126(6):1105-18. doi: 10.1016/j.jaci.2010.10.008. No abstract available.
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- H-25096489
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有時間枠
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- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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