Trial to Describe the Safety and Immunogenicity of Fluzone®
| Status: | Completed |
|---|---|
| Conditions: | Influenza |
| Therapuetic Areas: | Immunology / Infectious Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | August 2007 |
| End Date: | December 2007 |
Immunogenicity and Safety of the Inactivated, Split-Virion Influenza Vaccine, Northern Hemisphere 2007-2008 Formulation (Intramuscular Route)
Objective 1:To describe the safety of the inactivated, split-virion influenza vaccine,
Northern Hemisphere (NH) 2007-2008 formulation.
Objective 2: To describe the immunogenicity, of Fluzone, inactivated, split virion influenza
vaccine NH 2007-2008 formulation.
Objective 3: Serum Collection - To submit remaining available sera to Center for Biologics
Evaluation and research (CBER) for further analysis by the Food and Drug Administration
(FDA), the Center for Disease Control and Prevention (CDC), and the World Health
Organization (WHO) to support selection and recommendation of antigen strains for subsequent
influenza vaccines.
Northern Hemisphere (NH) 2007-2008 formulation.
Objective 2: To describe the immunogenicity, of Fluzone, inactivated, split virion influenza
vaccine NH 2007-2008 formulation.
Objective 3: Serum Collection - To submit remaining available sera to Center for Biologics
Evaluation and research (CBER) for further analysis by the Food and Drug Administration
(FDA), the Center for Disease Control and Prevention (CDC), and the World Health
Organization (WHO) to support selection and recommendation of antigen strains for subsequent
influenza vaccines.
Inclusion Criteria:
- Participant aged 18 years or older on the day of inclusion.
- Participant able to attend scheduled visits and to comply with the study procedures
during the entire duration of the study.
- Participant is in good health as assessed by the investigator.
- Participant willing and able to meet protocol requirements.
- Participant willing and able to give informed consent.
- For a woman, inability to bear a child or negative serum/urine pregnancy test.
Exclusion Criteria:
- Self-reported allergy to egg proteins, chicken proteins, or one of the constituents
of the vaccine, such as thimerosal or formaldehyde.
- An acute illness with or without fever (temperature ≥ 99.5 °F oral) in the 72 hours
preceding enrollment in the trial.
- Clinically significant findings in vital signs (including temperature ≥ 99.5 °F oral)
on review of systems.
- Self-reported history of severe adverse event to any influenza vaccine.
- Laboratory-confirmed influenza infection or vaccination against influenza in the 6
months preceding enrollment in the study.
- Any vaccination in the 14 days preceding enrollment in the study or scheduled between
Visit 1 and Visit 2.
- Participation in any other interventional drug or vaccine trial within the 30 days
preceding or during enrollment into this study.
- Immunocompromising or immunosuppressive therapy (including systemic steroid use for 2
weeks or more), cancer chemotherapy, or radiation therapy at the time of enrollment,
planned during the period of this study, or at any time within the past 6 months.
- Receipt of blood or blood products within the 3 months preceding enrollment in the
study.
- Diabetes mellitus requiring pharmacological control.
- 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.
- Person deprived of freedom by an administrative or court order (having legal or
medical guardian).
- For women of childbearing potential, a positive urine pregnancy test, breast feeding,
or not using a medically approved form of contraception for the duration of the
trial.
- Current alcohol or drug use that may interfere with the subject's ability to comply
with trial procedures.
- Thrombocytopenia or bleeding disorder contraindicating intramuscular vaccination.
- Prior personal history of Guillain-Barré syndrome.
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