An interventional study of Oral immunotherapy with peanut in Peanut Allergic Subjects, Peanut Allergies and Peanut Hypersensitivity, sponsored by Laura Ozer Kettner. Not yet recruiting at 5 sites in Denmark. Open to participants aged 6 Months to 48 Months. Per ClinicalTrials.gov, last updated 2026-10-26.
Sponsored by Laura Ozer Kettner · Not applicable, Interventional, and Treatment
This clinical trial aims to investigate if oral immunotherapy can help children with peanut allergy tolerate peanut.
Children aged 6 months to 4 years can take part in the trial.
Main question: What percentage of children can tolerate peanut after oral immunotherapy, compared with children who avoid peanut?
Children are assigned to these two groups by chance.
Children receiving oral immunotherapy will:
All children will:
154 studies on the registry are indexed under Peanut Hypersensitivity; 27 are open to participants now.
This study's planned enrollment of 56 is above the median of 49 across 118 interventional studies indexed under Peanut Hypersensitivity.
Browse Peanut Hypersensitivity studies →Laura Ozer Kettner is the lead sponsor of 3 studies on the registry; 3 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Children randomized to oral immunotherapy will ingest a daily dose of peanut. Dose escalation will be performed approximately every two weeks at the allergy clinic or via online consultations. After approximately 6 months, a maintenance dose of 300 mg food protein will be reached and continued daily for 6-12 months.
Other: Oral immunotherapy with peanut
Children randomized to avoidance will receive standard care for peanut allergy, namely avoidance of peanut.
Oral immunotherapy with peanut for 1-1.5 years
Tolerance to peanut (4000 mg)
Proportion of children who tolerate a cumulative dose of 4000 mg of peanut protein at an oral food challenge
Time frame: 1-1.5 years after enrollment
Tolerance to peanut (1000 mg)
Proportion of children who tolerate a cumulative dose of 1000 mg of peanut protein at an oral food challenge
Time frame: 1-1.5 years after enrollment
Eliciting dose
Change in cumulative eliciting dose at an oral food challenge (mg peanut protein)
Time frame: At enrollment and 1-1.5 years after enrollment
Allergic reactions
Proportion of children experiencing allergic reactions to peanut outside the oral food challenge, the number of reactions per child, and the severity of the reactions (World Allergy Organization grading system, grade 1-5; higher grades indicate more severe reactions)
Time frame: 6 months, 1-1.5 years, and 2-2.5 years after enrollment
Use of adrenaline auto-injector
Proportion of children for whom an adrenaline auto-injector was used due to allergic reactions to peanut outside the oral food challenge, and the number of uses per child
Time frame: 6 months, 1-1.5 years, and 2-2.5 years after enrollment
Severity of allergic reactions at the oral food challenge according to the World Allergy Organization Grading System
Severity of allergic reactions to peanut at the oral food challenge, graded by the World Allergy Organization grading system (grade 1-5; higher grades indicate more severe reactions)
Time frame: 1-1.5 years after enrollment
Parental food allergy-related quality of life
Changes in quality of life scores measured by the Food Allergy Quality of Life - Parental Burden Questionnaire (FAQL-PB). Total scores range from 0 to 102, with higher scores indicating worse food allergy-related quality of life
Time frame: At enrollment, 1-1.5 years, and 2-2.5 years after enrollment
Parental food allergy-related anxiety
Changes in anxiety scores measured by the Impairment Measure for Parental Food Allergy-Associated Anxiety and Coping Tool (IMPAACT). Total scores range from 0 to 196. Subscale scores are also reported: Cognitive subscale (range 9 to 63), Behavioral subscale (range 9 to 63), Anxiety impact (range 8 to 56), and Child coping (range 2 to 14). For all scores, higher values indicate greater food allergy-related burden.
Time frame: At enrollment, 1-1.5 years, and 2-2.5 years after enrollment
Changes in specific immunoglobulin E (IgE)
Changes in peanut-specific IgE (kU/L)
Time frame: At enrollment, 1-1.5 years, and 2-2.5 years after enrollment
Characterization of allergic reactions during oral immunotherapy
The anticipated cause, the treatment received, the timing, and whether the reaction followed a dose increase
Time frame: During oral immunotherapy up-dosing and maintenance phase
Duration of oral immunotherapy up-dosing phase
The duration of the up-dosing phase, and the reasons for deviations from the planned schedule
Time frame: End of up-dosing phase (approximately 6 months after enrollment)
Study dropout
Proportion of children who dropped out, the phase of the study at dropout, and the reasons for dropout
Time frame: 6 months, 1-1.5 years, and 2-2.5 years after enrollment
Missed oral immunotherapy doses
Proportion of missed oral immunotherapy doses, and the reasons for missed doses
Time frame: 6 months and 1-1.5 years after enrollment
Long-term tolerance of peanut
Proportion of participants who still tolerate peanut among those whose peanut allergy resolved 1-1.5 years after enrollment
Time frame: 2-2.5 years after enrollment
Frequency of peanut intake
Frequency of peanut intake (daily, weekly, monthly or less than monthly) among participants whose peanut allergy resolved 1-1.5 years after enrollment
Time frame: 2-2.5 years after enrollment
Is oral immunotherapy worth it
Proportion of families who considered oral immunotherapy worthwhile, and their reported key benefits and burdens
Time frame: 1-1.5 years and 2-2.5 years after enrollment
Decisional conflict
Scores on the Decisional Conflict Scale. Total scores range from 0 to 100, with higher scores indicating greater decisional conflict
Time frame: Right after the shared decision-making process using the decision aid
Eosinophilic esophagitis
Proportion of children with symptoms suggestive of eosinophilic esophagitis, and the proportion with a biopsy-confirmed diagnosis
Time frame: 1-1.5 years after enrollment
Plan to share: No — Individual participant data will not be shared due to ethical and data protection considerations
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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Laura Ozer Kettner