Phase 4
Completed N=114
A Re-licensing Study to Assess the Efficacy of Inflexal V Formulated With WHO Recommended 2009/2010 Influenza Virus Strains for the Northern Hemisphere
Source: ClinicalTrials.gov NCT01306253 ↗Enrolled (actual)
114
Serious AEs
0.0%
Results posted
Jan 2012
Primary outcomePrimary: Seroconversion — 29; 32; 37; 35 Number of subjects
Summary
This study is to assess whether the Northern Hemisphere 2009/2010 season influenza vaccine Inflexal V fulfills the EMEA requirements for re-registration of influenza vaccines.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Seroconversion |
29; 32; 37; 35; 34; 33 | — |
| PRIMARY Seroprotection |
47; 47; 49; 51; 51; 46 | — |
| PRIMARY Fold Increase in Geometric Mean Titer (GMT) |
9.60; 5.93; 9.25; 8.30; 7.91; 6.93 | — |
| SECONDARY Safety: Numbers of Subjects Reporting Solicited Local Adverse Events |
1; 0; 5; 3; 1; 2 | — |
| SECONDARY Numbers of Subjects Reporting Solicited Systemic Adverse Events |
1; 0; 0; 0; 0; 0 | — |
Eligibility Criteria
Inclusion Criteria
- Healthy female and male adults
- Aged ≥18 to ≤60 years or >60 years on Day 1
- Written informed consent
Exclusion criteria
- Acute exacerbation of bronchopulmonary infection (cough, sputum, lung findings) or other acute disease
- Acute febrile illness (≥38.0 °C)
- Prior vaccination with an influenza vaccine in the past 330 days
- Known hypersensitivity to any vaccine component
- Previous history of a serious adverse reaction to influenza vaccine
- History of egg protein allergy or severe atopy
- Known blood coagulation disorder
- Chronic (longer than 14 days) administration of immunosuppressants or other immune-modifying drugs within 6 months before the first dose of study vaccine, incl. oral corticosteroids in dosages of ≥0.5 mg/kg/d prednisolone or equivalent (inhaled or topical steroids are allowed)
- Known immunodeficiency (incl. leukemia, cancer, HIV seropositivity)
- Investigational medicinal product received in the past 3 months (90 days)
- Treatment with immunoglobulins or blood transfusion(s) received in the past 3 months (90 days)
- Pregnancy or lactation
- Participation in another clinical trial
- Employee at the investigational site, or relative or spouse of the investigator
- Suspected non-compliance
Data sourced from ClinicalTrials.gov (NCT01306253). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.