Tolerability and Immunogenicity Study of FLUVAL P H1N1 Flu Vaccine of Omninvest in Children and Adolescents
Tolerability and Immunogenicity Study of FLUVAL P H1N1 Monovalent Influenza Vaccine of Omninvest in Children and Adolescents
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Primary Objective:
- To assess tolerability/safety (incidence of adverse events 21-28 days following vaccination) of the study drug.
Secondary Objectives:
- To assess the efficacy (immunogenicity) of the study drug by serology testing of blood samples taken at Day 21-28 after immunization in groups and age groups.
- To assess long term (180-210 days following vaccination) tolerability/safety (incidence of adverse events) of the study drug.
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Veszprém, Hungary, 8200
- "Csolnoky Ferenc" Veszprém County Hospital
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Children aged 3 to 12 years, adolescents aged 12 to 18 years, both sexes;
- Are in good health (as determined by vital signs and existing medical condition) or are in stable medical condition. Subjects will not be excluded with known adequately treated clinically significant organ or systemic diseases (e.g. asthma or diabetes)m such that, in the opinion of the investigator, the significance of the disease will not compromise the subject's participation in the study.
- Female volunteers of childbearing potential with a negative result from the urine pregnancy test prior to vaccination who agrees to use an acceptable contraception method (includes implants, injectibles, combined oral contraceptives, effective intrauterine devices /IUDs/, sexual abstinence, or a vasectomized partner) or abstinence throughout the trial and not become pregnant for the duration of the study.
- Capability of adolescent participants aged 12 to 18 years and the legitimate representative of all volunteers to understand and comply with planned study procedures;
- Absence of existence of any exclusion criteria.
Exclusion Criteria:
- Pregnancy or breast feeding or positive urine pregnancy test at baseline prior to vaccination;
- Known allergy to eggs or other components of the vaccine (in particular mercury);
- History of Guillain-Barré syndrome;
- Active neoplasm (i.e. requiring any form of anti-neoplastic therapy);
- Immunosuppressive therapy in the preceding 36 months;
- Concomitant corticosteroid therapy, including high-dose inhaled corticosteroids (local corticosteroid or corticosteroid nasal spray are permitted);
- Immunoglobulin (or similar blood product) therapy within 3 months prior to vaccination;
- Documented HIV, HBV or HCV infection;
- Chronic illness that, in the opinion of the investigator, may interfere with the evaluation of the immunoresponse;
- Acute febrile respiratory illness within one week prior to vaccination;
- Vaccine therapy within 4 weeks prior to vaccination;
- Influenza vaccination within 6 months prior to vaccination;
- Experimental drug therapy within 1 month prior to vaccination;
- Past or current psychiatric disease of the volunteer or the legitimate representative that upon judgement of the investigator may have effect on the objective decision-making of the volunteer or the legitimate representative;
- Alcohol or drug abuse of the participant or the legitimate representative.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Active Comparator: Vaccination with Fluval AB Novo
|
Other Names:
|
|
Active Comparator: Vaccination with Fluval AB
|
Other Names:
|
|
Experimental: Vaccination with Fluval P
|
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Incidence of adverse events
Time Frame: 21-28 days after vaccination
|
21-28 days after vaccination
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Post vaccination HI antibody titer
Time Frame: 21-28 days after vaccination
|
21-28 days after vaccination
|
|
Incidence of adverse events
Time Frame: 180-210 days after vaccination
|
180-210 days after vaccination
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Director: Anna Ősi, Dr., Omninvest Ltd.
- Principal Investigator: Éva Szabó, MD, "Csolnoky Ferenc" Veszprém County Hospital
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- FLUVAL P-H-07
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