Influenza
Conditions
Keywords
Influenza
Brief summary
Prospective study to evaluate the safety and immunogenicity of Butantan Influenza seasonal vaccine.
Detailed description
Prospective cohort study to evaluate safety (three days post vaccination) and immunogenicity (measured 21 days post vaccination) of one dose of Butantan Influenza vaccine.
Interventions
Butantan Fragmented Inactivated Trivalent Influenza Vaccine
Sponsors
Butantan Institute
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Healthy adults, male or female aged 18 to 59 * Elderly aged 60 years completed and above * To be available to participate in the study throughout its duration (approximately 21 days) * To have medical indication to be vaccinated against influenza * To demonstrate intention to participate in the study, as documented by signature in the study´s informed consent form.
Exclusion criteria
* Evidence of active neurological, cardiac, pulmonary, hepatic or renal disease as clinical history and/or physical examination (except hypertension under control among the elderly) * Compromised immune system diseases including: HIV, diabetes mellitus, cancer (except basal cell carcinoma) and autoimmune diseases * Behavioral, cognitive or psychiatric disease that in the opinion of the principal investigator or his representative physician, affects the participant ability to understand and cooperate with all study protocol requirements * Abusive usage of alcohol or drugs in the past 12 months that has caused medical, professional or family problems, indicated by clinical history * Known systemic hypersensitivity to eggs or to any component of the vaccine * History of severe adverse reaction after previous administration of an Influenza vaccine within 6 weeks following vaccination * History of Guillain-Barre Syndrome or other demyelinating disease * Diagnosis of asthma with a history of hospitalization in the last six months due to illness * Suspected or confirmed fever in the 3 days prior to vaccination or axillary temperature greater than 37.8 ° C on the day of vaccination * Use of corticosteroids (except topical or nasal) or other immunosuppressive drugs within 42 days before study initiation/baseline. It will be considered immunosuppressive dose of corticosteroids the equivalent to a dose ≥10 mg of prednisone per day for over 14 days * Impaired coagulation due to chronic disease or due to use anticoagulant medication (warfarin or heparin) in the 7 days preceding vaccination * Have received live virus vaccine within 28 days or killed virus vaccine in the last 14 days prior to vaccination, or have a scheduled immunization during the first 21 days after vaccination * Have received influenza vaccine in the past 6 months; * History of asplenia * Have received blood products in the past 6 months, including transfusions or immunoglobulin, or scheduled administration of blood products or immunoglobulin for the first 21 days after vaccination * have a counter indication for Influenza vaccination, including allergy to egg proteins * Use of any investigational product within 42 days before vaccination; * Any other condition that might put in risk the safety/rights of a potential participant or hurdle his/her compliance with this protocol in investigator's opinion or his representative physician.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety assessed by unsolicited local and systemic adverse reactions | 3 days | Vaccine safety assessed by unsolicited local and systemic adverse reactions up to 3 days post vaccination |
| Antibody response to each of the vaccine´s strains (Immunogenicity) | 21 days | Antibody response to each of the vaccine´s strains as measured by % seroconversion, and/or increase in the geometric mean of hemagglutination inhibition (HAI) titers and/or % seroprotection. |
Countries
Brazil
Outcome results
None listed