FluMist in Egg Allergic Patients

NCT01248208 | Completed Phase 1 DMC

• 1 other identifier: 357349
• Study Type: interventional
• Target: 17
• Locations: 1 country
• Sites: 1

Brief Summary

With the growing public health concerns of seasonal influenza and H1N1 in the United States, the primary means by which this can be addressed is with prevention, namely, vaccination against the influenza virus. The only individuals not able to receive this vaccination in the primary care provider's office are those patients with egg allergies and, in rare circumstances, individuals with allergies to other components of the vaccine. Current guidelines allow for the administration of the influenza vaccine to patients with egg allergy using vaccines with low egg protein (ovalbumin) content or by using skin testing followed by a 5-dose desensitization protocol. Since this is impractical to perform in the primary care office and cumbersome for allergists, many egg-allergic patients simply do not receive the influenza vaccine, leaving them more vulnerable to the disease and more likely to become a source of contagion. Several studies have suggested that influenza vaccination using a 1-2 dose protocol may be safe. This fact is due in large part to the low ovalbumin (egg protein) content in modern influenza vaccines. All studies of influenza vaccination in egg-allergic patients have been done using intramuscular trivalent inactivated influenza vaccine (TIV). However, the trivalent live-attenuated, cold-adapted influenza vaccine (LAIV), which is delivered intranasally, has a lower published ovalbumin content than the injectable vaccines, suggesting that it may also be well-tolerated by egg-allergic patients. According to several studies, LAIV may be more efficacious than TIV in children. It is the goal of the investigators to evaluate the safety of immunizing egg-allergic individuals with the LAIV.

Conditions

Egg Allergy; Eligible for Vaccination Against Influenza

Keywords

egg allergy; influenza vaccine

Outcome Measures

Primary Outcomes (1)

• To estimate the safety of LAIV in egg-allergic patients receiving the LAIV.

  within 48 hours after vaccine administration

Secondary Outcomes (1)

• To estimate the safety of a single, full-strength dose of TIV in egg allergic patients.

  Within 48 hours of vaccination

Study Arms (2)

FluMist (LAIV) group

EXPERIMENTAL

FluMist influenza vaccine 0.2 mL intranasal vaccine once

Biological: FluMist intranasal influenza vaccine

Flu shot (TIV) group

ACTIVE COMPARATOR

Patients 6 months to 2 yrs or \> 49 years or WITH a history of asthma symptoms / treatment within the past 12 months will receive intramuscular influenza vaccination. History/Treatment of asthma in the past 12 months is defined as follows: 1. wheezing in the past 12 months 2. use of inhaled corticosteroids (ICS), combined ICS / long acting beta agonist (LABA), or oral steroid in the past 12 months 3. emergency room or acute care visit or hospitalization for asthma or wheezing in the past 12 months.

Biological: Intramuscular influenza injection ("flu shot")

Interventions

FluMist intranasal influenza vaccine BIOLOGICAL

FluMist intranasal vaccine 0.2 mL will be given 0.1 mL in each nostril per manufacturer's instructions.

FluMist (LAIV) group

Intramuscular influenza injection ("flu shot") BIOLOGICAL

Subjects \< 2 years or \> 49 years or those with asthma symptoms or treatment within the past year will receive the intramuscular flu shot in a single injection. Age 6-36 months: 0.25 mL IM x 1; Age \>36 months: 0.5 mL IM x 1 Boosters: All children aged 6 months-8 years who receive a seasonal influenza vaccine for the first time should be administered 2 doses. Children aged 6 months-8 years who received a seasonal vaccine for the first time during 2009-2010 but who received only 1 dose should receive 2 doses, rather than 1, during 2010-2011. In addition, for the 2010-11 influenza season, children aged 6 months-8 years who did not receive at least 1 dose of an influenza A (H1N1) 2009 monovalent vaccine should receive 2 doses of a 2010-11 seasonal influenza vaccine, regardless of previous influenza vaccination history. For all children, the second dose of a recommended 2-dose series should be administered 4 or more weeks after the initial dose.

Also known as: Fluzone (approved for children down to 6 months), Fluvirin (age 4y and older), Agriflu (age 18y and older), Fluarix (age 3y and older), FluLaval (age 18y and older), Afluria (age 9y and older)

Flu shot (TIV) group

Eligibility Criteria

• Age: 6 Months+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Age \> 6 months
• Clinical history of allergic symptoms (hives, swelling, vomiting, respiratory problems, low blood pressure) within 2 hours after ingestion of egg OR Eczema/atopic dermatitis worsened by egg exposure
• Confirmation of clinical history by positive egg skin prick test or serum egg-specific IgE or a positive oral food challenge. \[The \>95% positive predictive values of egg serum IgE in subjects \>2 years old with atopic dermatitis is 6 kU/L or greater. In subjects \>2 years old without atopic dermatitis, the value is 7 kU/L or greater. In subjects less than 2 years old, the value is 2 kU/L or greater.\]
• FluMist (LAIV) cohort: Patients age 2-49 years WITHOUT a history of asthma symptoms or treatment within the past 12 months will receive intranasal FluMist.
• Flu Shot (TIV) Intramuscular influenza vaccine cohort: Patients 6 months to 2 yrs or \> 49 years or WITH a history of asthma symptoms / treatment within the past 12 months. History/Treatment of asthma in the past 12 months is defined as follows:
• wheezing in the past 12 months
• use of inhaled corticosteroids (ICS), combined ICS / long acting beta agonist (LABA), or oral steroid in the past 12 months
• emergency room or acute care visit or hospitalization for asthma or wheezing in the past 12 months.

You may not qualify if:

• Subjects who potentially have outgrown their egg allergy (no allergic reaction with ingestion of whole egg in the past 18 months and an egg serum specific IgE level ≤2 kU/L).
• Pregnancy
• Current moderate to severe illness with a fever.
• Allergy to other components of the vaccine - gentamicin, gelatin, arginine, thimerosal - or a history of a previous allergic reaction to the influenza vaccine.
• Abnormal Vital Signs.
• History of Guillain-Barre' Syndrome (GBS).
• HIV/AIDS or another disease that affects the immune system, or cancer.
• Long term health problems that are contraindicated for the LAIV or TIV.
• Receipt of a live viral vaccine within the month prior (e.g. FluMist, MMR, yellow fever, chicken pox, rotavirus, smallpox).
• Current use of any prescription medicine (e.g. antiviral) to prevent or treat influenza. (only excludes use of LAIV, may still receive TIV)
• Concurrent use of aspirin or aspirin-containing therapy in children and adolescents (2-18 years of age)(only excludes use of LAIV, may still receive TIV)
• Living with or having close contact with someone whose immune system is severely compromised (e.g. transplant recipient). (only excludes use of LAIV, may still receive TIV) Breastfeeding mothers may still receive either LAIV or TIV.
• The following medications can interfere with signs of an allergic reaction or complicate the treatment of an allergic reaction and should be discontinued as outlined below:
• H1 antihistamines or doxepin should be discontinued for 7 days, and diphenhydramine for 72 hrs prior.
• H2 antihistamines should be discontinued for 24 hrs prior.

Sponsors & Collaborators

• Walter Reed Army Medical Center: lead
• University of Texas: collaborator
• University of South Alabama: collaborator
• University of Michigan: collaborator
• Scripps Clinic: collaborator

Study Sites (1)

Walter Reed Army Medical Center

Washington D.C., District of Columbia, 20307, United States

Location

Related Links

• CDC Information on Seasonal Influenza
• Food Allergy and Anaphylaxis Network

MeSH Terms

Conditions

Egg Hypersensitivity; Influenza, Human

Interventions

Influenza Vaccines; fluarix; FluLaval; Afluria

Condition Hierarchy (Ancestors)

Food Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases; Respiratory Tract Infections; Infections; Orthomyxoviridae Infections; RNA Virus Infections; Virus Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Viral Vaccines; Vaccines; Biological Products; Complex Mixtures

Study Officials

• Susan Laubach, MD

  Walter Reed Army Medical Center

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SINGLE GROUP
• Sponsor Type: FED
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Allergy & Immunology faculty

Study Record Dates

• First Submitted: November 24, 2010
• First Posted: November 25, 2010
• Study Start: September 1, 2010
• Primary Completion: September 1, 2011
• Study Completion: October 1, 2012
• Last Updated: October 3, 2018

Record last verified: 2018-10

Locations

US (1)