Clinical trial Recruiting at 1 site Observational

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.

More Egg Allergy trials

Quick facts

Study typeObservational
SexAll
Enrollment147 (estimated)
SponsorMurdoch Childrens Research Institute
Academic / other
Drugs / interventionsimmunotherapy
Locations1 site (Parkville, Victoria)
StatusRecruiting
StartedJanuary 13, 2026
Main results expectedJanuary 2027
Study endsJanuary 2027
Registry record updatedFebruary 2, 2026
Trial IDNCT07359183 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

  • 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

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.