Status:
COMPLETED
Study of Quadrivalent Influenza Vaccine Among Children
Lead Sponsor:
Sanofi Pasteur, a Sanofi Company
Conditions:
Influenza
Eligibility:
All Genders
6-8 years
Phase:
PHASE3
Brief Summary
The aim of the study is to evaluate a prototype quadrivalent influenza vaccine (QIV), the licensed 2010-2011 trivalent influenza vaccine (TIV) containing the primary B strain (B1), and the investigati...
Detailed Description
Participants will receive a single dose of their assigned vaccine during Visit 1. For those requiring two doses of influenza vaccine, as per Advisory Committee on Immunization Practices (ACIP) guidanc...
Eligibility Criteria
Inclusion
- Subject is 6 months to \< 9 years of age on the day of inclusion.
- Parent/guardian is willing and able to attend scheduled visits and to comply with the study procedures during the entire duration of the study.
- Subject is in reasonably good health as assessed by the Investigator.
- Informed consent is granted by the parent(s) or other legally acceptable representative; assent by subjects 7 to \< 9 years of age.
- For subjects 6 months to \< 24 months of age, born at full term of pregnancy (≥ 37 weeks) and with a birth weight ≥ 2.5 kg (5.5 lbs).
Exclusion
- History of allergy to egg proteins or any constituents of the vaccine.
- History of serious adverse reaction to any influenza vaccine.
- Any vaccination scheduled between Visit 1 and Visit 2 (or Visit 1 and Visit 3 for those requiring two doses).
- Receipt of any vaccine in the 4 weeks preceding the first study vaccination.
- Participation in another interventional clinical trial investigating a vaccine, drug, medical device, or medical procedure in the 4 weeks preceding the first study vaccination or during the course of the study.
- Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating intramuscular vaccination.
- Any condition that in the opinion of the Investigator would pose a health risk to the subject if enrolled or could interfere with the evaluation of the vaccine.
- Personal history of Guillain-Barré syndrome.
- Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months).
- Personal or immediate family history of congenital immune deficiency.
- Personal developmental delay, neurologic disorder, or seizure disorder.
- Any chronic illness that, in the opinion of the Investigator, is not well controlled and may interfere with trial conduct or completion, or with assessment of adverse events.
- Known seropositivity for human immunodeficiency virus, hepatitis B, or hepatitis C.
- Receipt of blood or blood-derived products (including immunoglobulin therapy) in the past 3 months, which might interfere with assessment of the immune response.
- Employees of the Investigator or study center, with direct involvement in the proposed study or other studies under the direction of that Investigator or study center, as well as family members of the employees or the Investigator.
Key Trial Info
Start Date :
November 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2012
Estimated Enrollment :
4363 Patients enrolled
Trial Details
Trial ID
NCT01240746
Start Date
November 1 2010
End Date
February 1 2012
Last Update
July 14 2015
Active Locations (67)
Enter a location and click search to find clinical trials sorted by distance.
1
Dothan, Alabama, United States, 36305
2
Chandler, Arizona, United States, 85224
3
Chandler, Arizona, United States, 85225
4
Mesa, Arizona, United States, 85203