NCT07192510

Brief Summary

Oral immunotherapy (OIT) using raw/ cooked egg has good desensitisation outcomes but is associated with frequent and sometimes severe adverse events (anaphylaxis is not uncommon). OIT using baked egg is less effective at inducing desensitisation but has a better safety profile. The compliance to daily consumption of baked egg products (muffins/ biscuits) after a negative baked egg challenge in egg allergic patients has also been reported to be poor, secondary to taste fatigue in children and need for frequent baking. A study using baked egg OIT had 38% withdrawal due to difficulties in ingesting the baked egg product daily. Pancakes, traditionally described as a flat cake prepared from a starch-based batter containing egg and milk and cooked on a hot surface for 5-7 minutes, is likely to be less allergenic than cooked egg because of the wheat matrix but more allergenic than baked egg. To date, there are no published studies investigating the use of pancakes in egg OIT. The investigators hypothesize that pancakes are more effective than baked eggs in inducing desensitisation and sustained unresponsiveness while reducing the risk of adverse events associated with egg OIT.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
23

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2021

Completed
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 16, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 16, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 25, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

September 25, 2025

Completed
Last Updated

September 25, 2025

Status Verified

September 1, 2025

Enrollment Period

4 years

First QC Date

August 25, 2025

Last Update Submit

September 17, 2025

Conditions

Keywords

oral immunotherapy

Outcome Measures

Primary Outcomes (1)

  • Proportion of participants achieving desensitisation - tolerating a cumulative dose of 4443 mg cooked egg protein

    12-18 months

Secondary Outcomes (5)

  • Proportion of participants achieving sustained unresponsiveness - tolerating a cumulative dose of 4443 mg cooked egg protein after 6-8 weeks of egg abstinence

    12-18 months

  • Number of treatment-related adverse reactions as assessed by CoFAR Grading

    12-18 months

  • Change in skin prick test wheal size to egg white

    12-18 months

  • Change in serum IgE levels to egg white, ovomucoid, ovalbumin

    12-18 months

  • Change in Food-Allergy Quality of Life Questionnaire (FAQL-Q) scores

    12-18 months

Study Arms (2)

Active

EXPERIMENTAL

Pancake Oral Immunotherapy

Other: Pancake oral immunotherapy

Control

NO INTERVENTION

Standard of care - strict egg avoidance

Interventions

The baked egg tolerant group underwent a 4-dose initial escalation (at intervals of 20-30 minutes) with pancakes in hospital (37.5 mg, 75 mg, 150 mg, 300 mg egg protein) to determine the home starting dose of pancake. The dose tolerated was one which resulted in no more than mild transient (not lasting more than 20 minutes) symptoms (e.g. itchy mouth) - transient Grade 1 symptoms. The home starting dose (taken daily at home) was one step below the tolerated dose, to minimise risk of allergic reactions at home, particularly as the presence of co-factors might decrease reaction threshold. Those reacting at 37.5 mg or 75 mg would not begin OIT with pancakes but instead began with cookies. Updosing visits were performed in the hospital at approximately 4 weekly intervals. Participants were kept at the pancake daily maintenance dose (2500 mg) for a minimum of 16 weeks, or total OIT duration of 18 months, whichever earlier

Also known as: OIT
Active

Eligibility Criteria

Age2 Years - 15 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Allergic to 4.443g egg protein or less, at baseline egg open food challenge OR Convincing clinical reaction to egg within past 6 months (or failed a clinical egg food challenge in last 6 months) AND evidence of current sensitization (positive SPT or egg-specific IgE performed within the last 3 months)

You may not qualify if:

  • Required previous admission to an intensive care unit for management of an allergic reaction.
  • Children with a past history of egg allergy currently consuming egg-containing products other than extensively-heated egg in baked foods (e.g. biscuits, cakes).
  • Developed severe anaphylaxis to egg or egg-containing products requiring more than 2 adrenaline auto-injectors or intravenous adrenaline infusion.
  • Poorly controlled asthma within the previous 3 months (as defined by clinician judgement with reference to the ICON guidelines).
  • Clinically significant chronic illness (other than asthma, rhinitis or eczema).
  • History of symptoms of eosinophilic oesophagitis, irrespective of cause.
  • Undergoing specific immunotherapy to another allergen and within the first year of treatment.
  • Receiving anti-IgE therapy, oral immunosuppressants, beta-blocker or ACE inhibitor.
  • Pregnancy.
  • Unwilling or unable to fulfil study requirements.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

KK Women's and Children's Hospital

Singapore, Singapore

Location

MeSH Terms

Conditions

Egg Hypersensitivity

Condition Hierarchy (Ancestors)

Food HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 25, 2025

First Posted

September 25, 2025

Study Start

April 1, 2021

Primary Completion

April 16, 2025

Study Completion

April 16, 2025

Last Updated

September 25, 2025

Record last verified: 2025-09

Locations