E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
No medical condition, healthy volunteers will be recruited into clinical trial for annual approval of influenza vaccine with the new strain composition accordng WHO and EMEA recommendation and CPMP criteria (CPMP/BWP/214/96) |
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MedDRA Classification |
E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
Immunogenicity Objectives To evaluate the antibody response to each influenza vaccine antigen, as measured by hemagglutination inhibition (HI) test on Day 0 and on Day 21, i.e., 21 days after vaccination in non-elderly adult and elderly subjects in compliance with the requirements of the current EU recommendations for clinical trials related to yearly licensing of influenza vaccines (CPMP/BWP/214/96). Antibodies may be additionally quantified using the SRH test for confirmation purposes. (Note for Guidance on Harmonisation of Requirements for Influenza Vaccines. CPMP/BWP/214/96: 12 March 1997).” Safety Objectives To evaluate safety of a single IM (intramuscular) dose of the split influenza vaccine Begrivac® in non-elderly adult and elderly subjects in compliance with the requirements of the current EU recommendations for clinical trials related to yearly licensing of influenza vaccines (CPMP/BWP/214/96).
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E.2.2 | Secondary objectives of the trial | |
E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
Subjects eligible for enrollment into this study are male and female adults who are 1. ≥ 18 years of age, mentally competent, willing and able to give informed consent prior to study entry 2. available for all the visits scheduled in the study and able to comply with all study requirements 3. in good health as determined by: - medical history - physical examination - clinical judgment of the investigator Written informed consent must be obtained from all the subjects before enrollment in the study after the nature of the study has been explained.
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E.4 | Principal exclusion criteria |
Subjects are not to be enrolled into the study if at least one of the following criteria is fulfilled: 1. They Have any serious (in the judgment of the investigator) disease, including but not limited to: a. Cancer, except for localized skin cancer b. Advanced congestive heart failure c. Chronic obstructive pulmonary disease (COPD) d. Autoimmune disease (including rheumatoid arthritis) e. Acute or progressive hepatic disease f. Acute or progressive renal disease g. Severe neurological or psychiatric disorder h. Severe Asthma 2. They have a history of any anaphylactic reaction and/or serious allergic reaction following a vaccination, a proven hypersensitivity to any component of the study vaccine (e.g., to ovalbumin, chicken protein, chicken feathers, influenza viral protein neomycin or polymyxin). 3. Known or suspected (or have a high risk of developing) impairment/alteration of immune function (excluding that normally associated with advanced age) resulting for example from: a. receipt of immunosuppressive therapy (any parental or oral cortical steroid or cancer chemotherapy/radiotherapy) within the past 60 days and for the full length of the study; b. Receipt of immunostimulants, c. Receipt of parenteral immunoglobulin preparation, blood products, and/or plasma derivatives within the past 3 months and for the full length of the study, d. Suspected or known HIV infection or HIV-related disease. 4. Known or suspected history of drug or alcohol abuse. 5. They have a bleeding diathesis or conditions associated with prolonged bleeding time that in the investigator’s opinion would interfere with the safety of the subject; 6. Women who are pregnant or woman of childbearing potential unwilling to practice acceptable contraception for the duration of the study (21 days). 7. Influenza vaccination or laboratory confirmed influenza within the last 6 months and more than one influenza vaccination within the past 12 months 8. Within the past 4 weeks they have received: - another vaccine - any investigational agent; 9. Any acute or chronic infection requiring systemic antibiotic treatment or antiviral therapy within the last 7 days. 10. They have experienced fever (i.e., axillary temperature ≥ 38°C) within the last 3 days 11. Simultaneous participation in another clinical study. 12. Any condition, which, in the opinion of the investigator, might prevent the subject from participation or interfere with the evaluation of the study objectives. 13. Severely obese with Body Mass Index (BMI) > 35 14. Site personnel involved in evaluation of safety and their immediate relatives are excluded from participation.
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E.5 End points |
E.5.1 | Primary end point(s) |
MEASURES OF IMMUNOGENICITY: Influenza antibody levels in serum measured by HI test on Days 0 and 21. Separately in each age group the following measures will be investigated: First, for each visit the number and proportion of subjects with a titre of antibodies of at least 40 (as measured by HI test) and the geometric means of titres (GMTs) will be determined. Second, the number and percentage of subjects with seroconversion or significant increse of titer as well as the mean geometric increase (GMT ratio) will be calcualted from these data.
MEASURES OF SAFETY: Incidences of local reactions (Days 0 to 3) including ecchymosis, erythema, induration, swelling and pain at the injection site summarized by maximal severity and by age group. Incidences of systemic reactions (Days 0 to 3) including chills/shivering, malaise, myalgia, arthralgia, headache, sweatinf, fatigue and fever summarized by maximal severity and by age group. Incidences of adverse events (including local and systemic rections with a duration beyond Day 3 post immunization) between Day 0 and study termination visit (Day 21, (-1/+5) summarized by each age group and by preferred term and system organ class (SOC). |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | Yes |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | No |
E.8.1.1 | Randomised | Information not present in EudraCT |
E.8.1.2 | Open | Information not present in EudraCT |
E.8.1.3 | Single blind | Information not present in EudraCT |
E.8.1.4 | Double blind | Information not present in EudraCT |
E.8.1.5 | Parallel group | Information not present in EudraCT |
E.8.1.6 | Cross over | Information not present in EudraCT |
E.8.1.7 | Other | Information not present in EudraCT |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | Information not present in EudraCT |
E.8.2.2 | Placebo | Information not present in EudraCT |
E.8.2.3 | Other | Information not present in EudraCT |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 2 |
E.8.5 | The trial involves multiple Member States | No |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | No |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.7 | Trial has a data monitoring committee | No |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | |
E.8.9.1 | In the Member State concerned months | 1 |
E.8.9.1 | In the Member State concerned days | |
E.8.9.2 | In all countries concerned by the trial months | 1 |