Long-term follow-up after 18 months of oral immunotherapy for peanut, egg, or milk allergy (5–15 years later)
Official title: Long Term Outcomes Associated With Attainment of Remission Following Oral Immunotherapy to Peanut, Egg and Cow's Milk (LPEM Study)
Run by Murdoch Childrens Research Institute · NCT07359183 · Data updated 2026-11-12
This follow-up will see if children and young people who completed an 18-month oral immunotherapy for peanut, egg, or milk allergy still have changes in allergy tests and better quality of life 5–15 years later.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 147 (estimated) |
| Sponsor | Murdoch Childrens Research Institute Academic / other |
| Drugs / interventions | immunotherapy |
| Locations | 1 site (Parkville, Victoria) |
| Status | Recruiting |
| Started | January 13, 2026 |
| Main results expected | January 2027 |
| Study ends | January 2027 |
| Registry record updated | February 2, 2026 |
| Trial ID | NCT07359183 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Children and young people who previously enrolled in PEAT, PrEMO, PPOIT-001, or PPOIT-002 and received at least one dose of OIT are ideal candidates.
✕Probably not a fit
People who did not receive OIT in the parent trials or who cannot safely provide blood or undergo skin testing are unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study invites former participants from four OIT parent trials (PEAT, PrEMO, PPOIT-001, PPOIT-002) for a single clinic visit 5–15 years after finishing an 18-month OIT course. Visits include a blood draw for specific IgE, storage of plasma and PBMC for future research, a skin prick test, and allergy and quality-of-life questionnaires. The primary comparison is long-term health-related quality of life and allergy status in participants who achieved remission versus those who did not. Eligibility requires prior participation in one of the listed parent trials and receipt of at least one OIT dose.
Why it matters
Potential benefit: If successful, the study could clarify whether OIT produces durable remission and sustained quality-of-life improvements years after treatment, informing long-term care decisions.
How similar studies have gone: Previous OIT trials have demonstrated short-term desensitization and some longer-term remission signals, but comprehensive 5–15 year follow-up data remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Previous participant of PEAT, PrEMO, PPOIT-001 or PPOIT-002 parent study * Received at least one dose of OIT treatment in the parent study * Written informed consent from participant and/or parent/guardian (if below 18 years of age) Exclusion Criteria: -Have any conditions that, in the opinion of the investigator, precludes participation for reason of safety
Where it's running
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Murdoch Children's Research Institute
Parkville, Victoria, Australia Recruiting
Study contacts
- Principal investigator: Adriana Chebar Lozinsky Rolnik — Murdoch Childrens Research Institute
- Study coordinator: Adriana Chebar Lozinsky Rolnik
- Email: lpem.study@mcri.edu.au
- Phone: 61399366435
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Rush versus conventional oral immunotherapy for cow's milk and hen's egg allergy in children
This test compares a faster 'rush' oral immunotherapy schedule with a conventional slower schedule to see which better helps children aged 6–16 with milk or egg allergy tolerate those foods.
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Remibrutinib for IgE-mediated peanut, milk, and egg allergy
This study tests whether remibrutinib can help people with peanut, milk, or egg allergies by comparing it to placebo over 52 weeks.
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LCA-0061 dose-ranging safety study for people with allergies
This Phase 1 study tests whether different single and multiple doses of LCA-0061 are safe and tolerable in people with atopy or peanut allergy, compared with placebo.
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MY006 to prevent severe allergic reactions from peanut exposure
MY006 injections will be tested to see if they prevent severe allergic reactions in adults and adolescents with peanut allergy.
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Home-based food challenges for adults with food allergies
This study is testing if it's safe and practical for adults with certain food allergies to try eating those foods at home instead of in a clinic.
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Maternal peanut and egg consumption versus avoidance during pregnancy and breastfeeding
This study will test whether mothers eating or avoiding peanuts and eggs from late pregnancy through breastfeeding changes babies' chances of developing peanut or egg allergies.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.