Skip to content

Safety of Nasal Influenza Immunisation in Egg Allergic Children

Phase 4 Study to Assess the Safety of Nasal Influenza Immunisation in Egg Allergic Children - a Multicentre Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01859039
Acronym
SNIFFLE
Enrollment
282
Registered
2013-05-21
Start date
2013-09-30
Completion date
2014-02-28
Last updated
2020-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Egg Hypersensitivity

Keywords

Egg allergy, Anaphylaxis, Children, Influenza vaccine

Brief summary

Egg allergy is common in early childhood, affecting at least one in 50 preschool children. Influenza ('flu) vaccines contain egg protein, as the vaccine is cultured in hen's eggs. There is robust data to support the safety of influenza vaccines (containing low or negligible amounts of egg protein) in patients with egg allergy. A new influenza vaccine, known as LAIV (Live Attenuated Intranasal Vaccine) has recently been approved by a number of licensing boards and is given by a spray into the nose. This new vaccine has been available in the United States for several years and is highly effective and against influenza infection, with an excellent safety profile in children without egg allergy. However, LAIV is also grown in hen's eggs and contains egg protein, and there are NO existing data on the safety of LAIV in egg-allergic children. The objective of this multicentre study is to assess the safety of intranasal LAIV in egg-allergic children, in order to demonstrate that these children can safely be given the new LAIV within a primary care health environment.

Interventions

BIOLOGICALAdministration of Live attenuated influenza vaccine

Sponsors

Imperial College London
CollaboratorOTHER
Public Health England
CollaboratorOTHER_GOV
University Hospital Southampton NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Aged 2 - 17 years old * Physician-diagnosis of egg allergy

Exclusion criteria

* Contraindicated as acutely unwell or current unstable asthma * Use of asthma reliever medication in last 72 hours * Recent administration of a medication containing antihistamine within the last 4 days * Current oral steroid for asthma exacerbation or course completed within last 2 weeks * Contraindications to ingredient in LAIV (notwithstanding allergy to egg protein) * Previous allergic reaction to an influenza vaccine * Children and adolescents who are clinically immunodeficient due to conditions or immunosuppressive therapy such as: acute and chronic leukaemias; lymphoma; symptomatic HIV infection; cellular immune deficiencies; and high-dose corticosteroids. * Children and adolescents younger than 18 years of age receiving salicylate therapy because of the association of Reye's syndrome with salicylates and wild-type influenza infection.

Design outcomes

Primary

MeasureTime frame
Incidence of allergic reaction to nasal influenza vaccination using a Live Attenuated Influenza Vaccine (LAIV) in egg-allergic childrenWithin 2 hours of vaccine administration

Secondary

MeasureTime frame
Incidence of delayed symptoms up to 72 hours after nasal influenza vaccination with LAIV in egg-allergic children72 hours after vaccine administration

Other

MeasureTime frameDescription
Incidence of immediate allergic reaction to LAIV in the subgroups described below.Within 2 hours of vaccine administration1. By age group 2-5, 5-11, 12-17 years 2. children with a previous history of anaphylaxis to egg protein, 3. children who have reacted previously to airborne traces of egg, 4. children who have egg allergy but are tolerant of baked egg, 5. Presence of physician-diagnosed asthma / recurrent wheeze 6. Presence of active allergic rhinitis to common environmental indoor allergens

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026