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Comparison of Inactivated and Live, Attenuated Influenza Vaccine in Children 5-9 Years of Age-Year 3 Amendment

Primary Purpose

Influenza

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
FluMist
Fluzone
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Influenza focused on measuring inactivated, attenuated, influenza vaccine, FluMist, Fluzone

Eligibility Criteria

5 Years - 9 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Healthy children aged 5-9 years of age. Parents willing to sign informed consent. Availability for follow-up for the planned duration of the study at least 4 weeks after last immunization. Acceptable medical history by screening evaluation and brief clinical assessment. Exclusion Criteria: History of immunodeficiency. Known or suspected impairment of immunologic function including, but not limited to, clinically significant liver disease; diabetes mellitus; moderate to severe kidney impairment. Household contact with immunodeficiency due to disease, medication or radiation. Child receiving aspirin therapy or aspirin-containing therapy. History of Guillain-Barré syndrome. Malignancy, other than squamous cell or basal cell skin cancer. Autoimmune disease. History of asthma or reactive airways disease. Chronic cardiovascular and pulmonary disorder. Chronic metabolic diseases (including diabetes), renal dysfunction or hemoglobinopathies requiring regular medical follow-up or hospitalization during the preceding year. Use of immunosuppressive medication. Corticosteroid nasal sprays are permissible. Medical or psychiatric condition or occupational responsibilities that preclude subject compliance with the protocol. Inactivated vaccine 14 days prior to vaccination. Live, attenuated vaccines within 60 days of study. Use of investigational agents within 30 days prior to study. Receipt of blood products or immunoglobulin in the past 6 months. Donation of the equivalent of a unit of blood within 6 weeks prior to enrollment. Acute febrile illness on the day of vaccination. Known allergies to any component of the vaccine, including thimerosal. History of allergy to eggs or egg products. Any condition that, in the opinion of the investigator, might interfere with study objectives.

Sites / Locations

  • Stanford University

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 26, 2005
Last Updated
August 26, 2010
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00138385
Brief Title
Comparison of Inactivated and Live, Attenuated Influenza Vaccine in Children 5-9 Years of Age-Year 3 Amendment
Official Title
A Randomized Comparison of the Immune Response to Either Inactivated or Live, Attenuated Influenza Vaccine in Children 5-9 Years of Age
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2007 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate how young children's bodies learn to fight against flu infection and to see how vaccines may help to fight against the flu. This is a Phase 4, single-center, randomized study of the immune responses of 40 children, ages 5-9, given one of two licensed influenza vaccines (either inactivated vaccine given in an arm muscle or live, attenuated vaccine inhaled through the nose). Study procedures will include up to 3 blood samples. Participants will complete a diary to document any side effects experienced following the vaccination. Participants will return to the clinic for a visit on Day 7-9 and again 4-6 weeks following vaccination. Participants that have not been previously vaccinated will receive a 2nd dose of vaccine. A follow up telephone call will occur 8-10 weeks following vaccination. Total study participation will be up to 75 days.
Detailed Description
This is a Phase 4, single-center, randomized clinical trial of the immune responses of children given one of two licensed influenza vaccines (either inactivated vaccine given IM or live, attenuated vaccine given intranasally). This study will enroll 40 healthy children 5-9 years of age. Subjects will be randomized to receive either FluMist or Fluzone. FluMist is approved for children older than 5 years and Fluzone is also approved for a broader age indication starting at 6 months of age. Subjects who receive FluMist will have the vaccine administered intranasally by large particle aerosol, 0.25 mL per nostril. Subjects receiving Fluzone will receive 0.5 mL given intramuscularly into the non-dominant deltoid muscle. Children who have not previously been immunized against influenza will receive a second dose of vaccine 4 weeks after the first dose. Children who receive two doses of vaccine will remain on the study for 8-10 weeks. The primary objective of this study is to compare the effector B cell responses at Day7-9 and the CD4 and CD8 T-cell responses, memory B-cell and the serology responses at Day 28 post-immunization following administration of one of two different influenza vaccines. Researchers will evaluate any increases in the immune response (CD4, CD8, B cell and serology responses) Day 0 to Day 7-9 for T-cells and ASCs, and from Day 0-28 for memory B-cell and serology responses. NK-cell and homing studies will also be compared between the groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Influenza
Keywords
inactivated, attenuated, influenza vaccine, FluMist, Fluzone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
FluMist
Intervention Type
Biological
Intervention Name(s)
Fluzone

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy children aged 5-9 years of age. Parents willing to sign informed consent. Availability for follow-up for the planned duration of the study at least 4 weeks after last immunization. Acceptable medical history by screening evaluation and brief clinical assessment. Exclusion Criteria: History of immunodeficiency. Known or suspected impairment of immunologic function including, but not limited to, clinically significant liver disease; diabetes mellitus; moderate to severe kidney impairment. Household contact with immunodeficiency due to disease, medication or radiation. Child receiving aspirin therapy or aspirin-containing therapy. History of Guillain-Barré syndrome. Malignancy, other than squamous cell or basal cell skin cancer. Autoimmune disease. History of asthma or reactive airways disease. Chronic cardiovascular and pulmonary disorder. Chronic metabolic diseases (including diabetes), renal dysfunction or hemoglobinopathies requiring regular medical follow-up or hospitalization during the preceding year. Use of immunosuppressive medication. Corticosteroid nasal sprays are permissible. Medical or psychiatric condition or occupational responsibilities that preclude subject compliance with the protocol. Inactivated vaccine 14 days prior to vaccination. Live, attenuated vaccines within 60 days of study. Use of investigational agents within 30 days prior to study. Receipt of blood products or immunoglobulin in the past 6 months. Donation of the equivalent of a unit of blood within 6 weeks prior to enrollment. Acute febrile illness on the day of vaccination. Known allergies to any component of the vaccine, including thimerosal. History of allergy to eggs or egg products. Any condition that, in the opinion of the investigator, might interfere with study objectives.
Facility Information:
Facility Name
Stanford University
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States

12. IPD Sharing Statement

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Comparison of Inactivated and Live, Attenuated Influenza Vaccine in Children 5-9 Years of Age-Year 3 Amendment

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