Quadrivalent Influenza Virus Vaccine
Conditions
Keywords
vaccine, safety, immunogenicity
Brief summary
This study evaluates the safety and immunogenicity of the quadrivalent influenza virus vaccine in healthy people aged years 3-60.Subjects will be randomly divided into 3 groups,receiving the test vaccine, commercially available trivalent influenza vaccine and trivalent influenza vaccine containing new influenza B component respectively. Each group has 800 subjects,2400 in total.
Interventions
BIOLOGICALone dose test vaccine
BIOLOGICALone dose commercially available trivalent influenza vaccine
Sponsors
Beijing Chaoyang District Centre for Disease Control and Prevention
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
3 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* healthy subjects more than 3 years old, and the subjects can be informed consent, and sign the informed consent. * the subjects and his guardians can obey the demands of the scheme . * Axillary temperature less than 37℃
Exclusion criteria
* The people who has flu or influenza-like symptoms(fever \<axillary temperature ≥38 ℃\>, cough or sore throat) within 3 months * The people who has vaccinated influenza vaccine in 3years. * The people who has a vaccine allergies, or who allergic to any kind of composition in experimental vaccine, such as eggs, ovalbumin etc. * The people who has serious side effects to vaccine, such as allergy, urticaria, skin eczema, dyspnea, angioneurotic edema or abdominal pain. * the subject who has symptoms of acute infection within a week. * Autoimmune diseases or Immune function defect, people has immunosuppressive therapy, cytotoxic treatment or inhaled corticosteroids in the past 6 months. * People has congenital malformations, developmental disorder or serious chronic diseases( such as Down's syndrome, diabetes, Sickle cell anemia or nerve system disease) * People has asthma Unstable that need emergency treatment, hospitalization, intubation, oral or intravenous corticosteroid in the past 2 years. * Diagnosed abnormal coagulation(Lack of clotting factors,Clotting disorders,Platelet abnormality) or significant bruising or coagulopathy * people has history or family history of convulsions, seizures, encephalopathy and psychiatric. * alienia, functional asplenia, and alienia or splenectomy in any situation. * Serious neurological disorders such as Green Barry syndrome. * people who has received blood products or immunoglobulin products in the past one months. * people who has received other study drug in the past one month. * people who received live attenuated vaccine, subunit vaccine or inactivated vaccine. * people who has received allergy treatment in in the past 14 days. * People who is on anti-TB treatment. * People whose axillary temperature is more than 37℃ before the vaccination. * People who is pregnant. * Any factors unsuitable for clinical trail according to the researchers.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Evaluate serum antibody titers of quadrivalent influenza Vaccine in healthy people. | 28 days | The serum antibody titers will be evaluated at 28 days after vaccination. |
| Evaluate the Rate of Adverse reactions of quadrivalent influenza Vaccine in healthy people. | 28 days | Adverse reactions associated with vaccine will be observed in subjects after vaccination. Solicited local adverse events include Pain, Redness, Swelling, Induration, Rash, Pruritus at injection site. solicited general adverse events include Fever, Nausea, Vomiting, Diarrhea, Decreased appetite, Be agitated (irritability, abnormal crying), fatigue, allergy. |
Outcome results
None listed