Study to Evaluate the Immune Responses of Trivalent Cold-Adapted Influenza Vaccine (CAIV-T) Compared With (TIV)

Influenza Clinical Trial

Official title:

A Prospective, Randomized, Open-Label Study to Evaluate the Immune Responses of Trivalent Cold-Adapted Influenza Vaccine (CAIV-T) Compared With Trivalent Inactivated Vaccine (TIV) in Children 6 to <36 Months of Age

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00111579
• Other study ID #: MI-CP123
• Status: Completed
• Phase: Phase 2
• First received: May 23, 2005
• Last updated: July 22, 2008
• Start date: May 2005
• Est. completion date: January 2006

Study information

• Verified date: July 2008
• Source: MedImmune LLC
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to describe the level of serum antibody conferred by CAIV-T and TIV against homotypic and heterotypic influenza virus strains.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: January 2006
• Est. primary completion date: January 2006
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 6 Months to 36 Months

Eligibility

Inclusion Criteria:

• Male or Female

• Ages 6 to but less than 36 months (reached their 6th month but have not yet reached their 3rd birthday) at the time of randomization

• Written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization (if applicable) obtained from the participant's parent/legal representative

• Ability of the parent/legal representative to understand and comply with the requirements of the study

• Parent/legal representative available by telephone

• Ability to complete follow-up period of 180 days after final study vaccination, as required by the protocol

Exclusion Criteria:

• History of hypersensitivity to any component of CAIV-T or TIV, including egg or egg products, monosodium glutamate, porcine gelatin or thimerosal

• History of hypersensitivity to gentamicin

• Any known immunosuppressive condition or immune deficiency disease (including HIV infection), or ongoing receipt of any immunosuppressive therapy

• Household contact who is immunocompromised (participants should also avoid close contact with immunocompromised individuals for at least 21 days after each study vaccination)

• History of Guillain-Barre syndrome

• Medically diagnosed wheezing, bronchodilator use, or steroid use (systemic or inhaled), by parent/legal representative report or chart review, within the 42 days prior to randomization (i.e., children with recent persistent asthma are excluded); or history of severe persistent asthma, according to the criteria described in the National Asthma Education and Prevention Program (NAEPP) Expert Panel Report: Guidelines for the Diagnosis and Management of Asthma - Update on Selected Topics 2002

• Acute febrile (not greater than 100.0 degrees F oral or equivalent) and/or clinically significant respiratory illness (e.g., cough or sore throat) within 72 hours prior to either study vaccination

• Use of aspirin or aspirin-containing products within 30 days prior to randomization, or expected use through 180 days after final study vaccination

• Receipt of any prior influenza vaccine

• Use of anti-influenza medications (including amantadine, rimantadine, oseltamivir, and zanamivir) within 14 days prior to randomization, or expected use through 180 days after final study vaccination

• Administration of any live virus vaccine within 30 days prior to randomization, or expected receipt through 30 days after final study vaccination

• Administration of any inactivated (i.e., non-live) vaccine within 14 days prior to randomization, or expected receipt within 14 days before, or 14 days after, either study vaccination

• Receipt of any investigational agent within 30 days prior to randomization, or expected receipt through 180 days after final study vaccination (use of licensed agents for indications not listed in the package insert is permitted)

• Receipt of any blood product within 90 days prior to randomization, or expected receipt through 180 days after final study vaccination

• Family member or household contact who is an employee of the research center or otherwise involved with the conduct of the study

• Any condition that, in the opinion of the investigator, would interfere with evaluation of the vaccine or interpretation of the study results

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Influenza
• Influenza, Human

Intervention

Biological:
• CAIV-T
A total vol. of 0.2 mL will be administered intranasally (approx. 0.1 mL into each nostril)for ea. of two doses.

Other:
• TIV
A total vol. of 0.25 will be administered intramuscularly for each of two doeses.

Locations

Country	Name	City	State
United States	Wee Care Pediatrics	Layton	Utah
United States	Bear Care Pediatrics	Ogden	Utah
United States	Alpine Pediatrics	Pleasant Grove	Utah
United States	Utah Valley Pediatrics	Provo	Utah
United States	Families First Pediatrics	South Jordan	Utah

Sponsors (1)

Lead Sponsor	Collaborator
MedImmune LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The following immunogenicity endpoints: The strain-specific HAI seroconversion rates (= 4-fold increase) among baseline seronegative participants (HAI titer = 1:4), by dose number		Day 28 post final vaccination	No
Primary	The proportion of participants achieving = 4-fold increase in strain-specific HAI titer from baseline in all participants regardless of baseline serostatus, by dose number		Day 28 post final vaccination	No
Secondary	Safety endpoints include: AEs SAEs and significant new medical conditions for all participants		Day 28 post vaccination	Yes