Safety and Immunogenicity of Two Doses of Monovalent Inactivated Influenza Vaccine That is Adjuvanted With MF59C.1 (MF59) and Uses a Surface Antigen From a Potential Pandemic Virus Strain Candidate (H5N1) in Adult and Elderly Subjects Using Four Different Vaccination Schedules

Novartis

Status and phase

Completed

Phase 3

Conditions

Pre-pandemic Influenza Vaccine

Treatments

Biological: Monovalent inactivated influenza vaccine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00848029

V87P12

2008-003008-72

Details and patient eligibility

About

The present study will evaluate the immunogenicity, safety and immunogenicity of two doses of monovalent inactivated influenza vaccine that is adjuvanted with MF59C.1 (MF59) and uses a surface antigen from a potential pandemic virus strain candidate (H5N1) in Adult Subjects.

Enrollment

240 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subjects aged 18 to 60 years of age who are mentally competent and who have signed an informed consent form after having received a detailed explanation of the study protocol;
In good health as determined by:
- Medical history,
- Physical examination,
- Clinical judgment of the Investigator;
Able to understand and comply with all study procedures and to complete study diaries, can be contacted, and will be available for all study visits.

Exclusion criteria

Previous receipt of any H5 vaccine;
Receipt of another investigational agent within 4 weeks, or before completion of the safety follow-up period in another study, whichever is longer, prior to enrollment and unwilling to refuse participation in another clinical study through the end of the study;
Experienced any acute disease or infection requiring systemic antibiotic or antiviral therapy (chronic antibiotic therapy for urinary tract prophylaxis is acceptable) within the past 7 days;
Experienced fever (defined as axillary temperature 38.0°C) within 3 days prior to Visit 1;
Pregnant or breastfeeding;
Females of childbearing potential who refuse to use an acceptable method of birth control for the duration of the study. Adequate contraception is defined as hormonal (e.g., oral, injection, transdermal patch, implant, cervical ring), barrier (e.g., condom with spermicide or diaphragm with spermicide), intrauterine device (e.g., IUD), or monogamous relationship with vasectomized partner who has been vasectomized for 6 months or more prior to the subject's study entry;
Any serious disease, such as:
- cancer,
- Autoimmune disease,
- diabetes mellitus,
- chronic pulmonary disease,
- acute or progressive hepatic disease,
- acute or progressive renal disease;
Surgery planned during the study period;
Bleeding diathesis;
Hypersensitivity to eggs, chicken protein, chicken feathers, influenza viral protein, neomycin or polymyxin or any other component of the study vaccine;
History of any neurological symptoms or signs following administration of any vaccine, or anaphylactic shock following administration of any vaccine;
Known or suspected impairment/alteration of immune function, for example, resulting from:
- Receipt of immunosuppressive therapy (any corticosteroid therapy
- Receipt of immunostimulants,
- High risk for developing an immunocompromising disease