Tolerability and Safety Study of FLUVAL P Monovalent Influenza Vaccine in Children
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Purpose
To determine the tolerability and safety of FLUVAL P monovalent influenza vaccine in children.
| Condition | Intervention |
|---|---|
|
Influenza |
Biological: Vaccination with FLUVAL P |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Tolerability and Safety Study of FLUVAL P Monovalent Influenza Vaccine in Children |
- Incidence of adverse events [ Time Frame: 28 days after vaccination ] [ Designated as safety issue: Yes ]To assess tolerability/safety (incidence of adverse events) of the study drug after Day 28 following the vaccination.
- Incidence of adverse events [ Time Frame: 180-210 days after vaccination ] [ Designated as safety issue: Yes ]To assess safety of the study drug after Day 180-210 following the vaccination.
- Efficacy of the study drug [ Time Frame: 180-210 days after vaccination ] [ Designated as safety issue: No ]To assess the efficacy of the study drug by epidemiological follow-up of the participants until Day 180-210 following the vaccination.
| Enrollment: | 10 |
| Study Start Date: | September 2009 |
| Study Completion Date: | May 2010 |
| Primary Completion Date: | April 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Vaccination with Fluval P
Vaccination with Fluval P monovalent influenza vaccine with 6 μg HA/0.5 ml active ingredient content and aluminium phosphate gel adjuvant. Dose: 0.25 ml (total 3 μg HA), single dose.
|
Biological: Vaccination with FLUVAL P
Vaccination with Fluval P monovalent influenza vaccine with 6 μg HA/0.5 ml active ingredient content and aluminium phosphate gel adjuvant. Dose: 0.25 ml (total 3 μg HA), single dose. Other Names:
|
Detailed Description:
This is an open, uncontrolled study to assess safety and tolerability of Fluval P monovalent influenza vaccine (whole virus, inactivated, adjuvanted with alumn phosphate gel) containing 6 mcgHA per 0.5mL active ingredient in children of 6-36 months of age. The vaccination is not repeated.
Tolerability and safety (incidence of adverse events) of the study drug is assessed after Day 28 then after Day 180-210 following the vaccination.
Eligibility| Ages Eligible for Study: | 6 Months to 36 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Children aged 6 to 36 months, 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), such that, in the opinion of the investigator, the significance of the disease will not compromise the subject's participation in the study;
- Capability of the legitimate representative of the volunteer to understand and comply with planned study procedures;
- Legitimate representative of the volunteer provide written informed consent prior to initiation of study procedures;
- Absence of existence of any exclusion criteria.
Exclusion Criteria:
- Known allergy to eggs or other components of the vaccine (in particular mercury);
- History of Guillain-Barré syndrome;
- Active neoplasm;
- Former or on-going immunosuppressive therapy;
- Concomitant corticosteroid therapy, including high-dose inhaled corticosteroids;
- 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 have effect on the participation in the study;
- 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 legitimate representative that upon judgement of the investigator may have effect on the objective decision-making of the legitimate representative;
- Alcohol or drug abuse of the legitimate representative.
Contacts and Locations| Hungary | |
| "Csolnoky Ferenc" Veszprém County Hospital | |
| Veszprém, Hungary, 8200 | |
| Study Director: | Anna Ősi, Dr. | Omninvest Ltd. |
| Principal Investigator: | Éva Szabó, MD | "Csolnoky Ferenc" Veszprém County Hospital |
More Information
No publications provided
| Responsible Party: | Omninvest Vaccine Manufacturing, Researching and Trading Ltd. |
| ClinicalTrials.gov Identifier: | NCT01100294 History of Changes |
| Other Study ID Numbers: | FLUVAL P-H-08 |
| Study First Received: | March 30, 2010 |
| Last Updated: | May 18, 2012 |
| Health Authority: | Hungary: National Institute of Pharmacy |
Keywords provided by Omninvest Vaccine Manufacturing, Researching and Trading Ltd.:
|
Influenza Pandemic vaccine Seasonal vaccine Prevention |
Influenza vaccine Influenza in humans Pandemic influenza in humans Influenza vaccine for children |
Additional relevant MeSH terms:
|
Influenza, Human Orthomyxoviridae Infections RNA Virus Infections Virus Diseases Respiratory Tract Infections Respiratory Tract Diseases Aluminum phosphate |
Antacids Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Adjuvants, Immunologic Immunologic Factors Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 22, 2013