Evaluate the Safety and Efficacy of Quadrivalent Influenza in Real-world Situations.
- Conditions
- GCP
- Interventions
- Biological: One dose of quadrivalent influenza virus split vaccine was administered
- Registration Number
- NCT06334510
- Lead Sponsor
- Hualan Biological Bacterin Co. Ltd.
- Brief Summary
To evaluate the inter-batch consistency (CI) of quadrivalent influenza vaccine (split virion) among healthy people aged 18-59 years； Secondly, to evaluate the safety and immunogenicity of quadrivalent influenza vaccine (split virion) in the expanded population aged 3 years and above, in order to observe the rare adverse reaction of 1‰.
- Detailed Description
The study was divided into two parts. The first part was an inter-batch consistency study (a randomized, double-blind, 1050 subjects aged 18-59 years). The second part was the safety and immunogenicity study in the expanded population aged 3 years and above (enrollment 4900).were selected to receive of normal commercially available quadrivalent influenza vaccine。 Safety observation: follow-up was conducted to observe the occurrence of AE within 30 minutes (0 day) and 0-30 days after vaccination, and the occurrence of SAE within 6 months after vaccination.
Immunogenicity observation: Blood samples were collected from all subjects before and 30 days after vaccination for influenza virus HI antibody detection。 According to the European Union seasonal influenza evaluation criteria, if the HI antibody seroconversion rate of each subtype of influenza virus was ≥40%, the HI antibody positive rate was ≥70%, and the GMI of each subtype of influenza virus was ≥2.5 times 30 days after any dose of vaccination, the vaccination schedule was considered to have acceptable immunogenicity.
Safety outcome MEASURES The occurrence of adverse reactions/events after each dose of vaccination was observed. The incidence of ① total adverse reactions/events, ② incidence of grade 3 or above adverse reactions/events and SAE, ③ incidence of adverse reactions/events severity classification, ④ incidence of adverse reactions/events by type (inoculation site and systemic, SOC, PT) and incidence of adverse reactions/events severity classification were calculated.
Note: Known adverse effects of quadrivalent influenza vaccine that have been identified in previous clinical studies are as follows:
Inoculation site (local) adverse events: pain, induration, swelling, rash, redness, pruritus, cellulitis.
Adverse events at non-inoculated sites (systemic) included fever, diarrhea, constipation, dysphagia, anorexia, vomiting, nausea, myalgia (non-inoculated sites), arthralgia, headache, cough, dyspnea, pruritus at non-inoculated sites (without skin lesions), mucocutaneous abnormalities, irritation/inhibition, acute anaphylaxis, and fatigue/fatigue.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 4900
- Healthy people aged 3 years and above;
- I (or/and his/her legal guardian/authorized representative) can comply with the requirements of the clinical trial protocol after informed consent and voluntary signed informed consent;
- No contraindications of quadrivalent influenza vaccine in the package insert and meet the vaccination requirements after medical history inquiry.
- Allergy to any component of the quadrivalent influenza vaccine, including egg, excipients, formaldehyde, or Triton X-100;
- people with a history of anaphylaxis after vaccination (allergy to any previous vaccination);
- Acute disease, severe chronic disease, acute onset of chronic disease, cold and fever;
- Axillary body temperature ≥37.3℃ (> 14 years old) and ≥37.5℃ (≤14 years old) before vaccination;
- Uncontrolled epilepsy;
- patients with progressive neurological disease or a history of Guillain-Barre syndrome;
- receiving immunoglobulin injection for less than one month;
- vaccination with live attenuated vaccine within 14 days before and other vaccines within 7 days before vaccination;
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Approval consistency study One dose of quadrivalent influenza virus split vaccine was administered A total of 1050 recipients aged 18-59 years were enrolled in this study. Blood samples were collected before and 30 days after vaccination. Hemagglutination inhibition (HI) antibody to influenza virus was detected in the serum of all recipients to evaluate the inter-batch consistency of the vaccine. Safety and immunogenicity in a larger vaccination cohort aged 3 years and older One dose of quadrivalent influenza virus split vaccine was administered 3850 recipients were enrolled in an open trial: safety observation after vaccination, follow-up for adverse events (AE) 30 minutes and 0-30 days after vaccination, and SAEs for 6 months after vaccination.
- Primary Outcome Measures
Name Time Method To evaluate the safety and immunogenicity of Hualan Biovar quadrivalent influenza vaccine in a larger population in the real world, and to observe rare adverse drug reaction (ADR) of 1‰. The safety was observed until 6 months after the full course of immunization The incidence of adverse events/reactions after quadrivalent influenza vaccination was observed, and the incidence of ① total adverse events/reactions, ② incidence of grade 3 or above adverse events/reactions and SAE, ③ incidence of adverse events/reactions according to severity classification of adverse events/reactions and ④ incidence of symptomatic adverse events/reactions were calculated.
- Secondary Outcome Measures
Name Time Method To explore the consistency of three consecutive batches of commercial vaccines for vaccination in adults aged 18-59 years. Before and 30 days after immunization The lower limit of the 95% confidence interval (CI) of the seroconversion rate (SCR) of hemagglutination inhibition (HAI) antibodies against each virus strain after vaccination was ≥40%. The lowest dilution used in the assay was 1 in 10. Seroconversion was defined as a prevaccination HAI titer of \<1:10 and a postvaccination titer of ≥1:40 or a prevaccination titer of ≥1:10 and a 4-fold or greater increase in titer after vaccination.
Trial Locations
- Locations (1)
Kou Zengqiang
🇨🇳Jinan, Shandong, China