Influenza Clinical Trial
Official title:
An Open-Label Exploratory Clinical Study to Evaluate the Antibody and Cell Mediated Immunity of One Intramuscular Dose of MF59-Adjuvanted Egg-Derived, Inactivated Novel Swine Origin A/H1N1 Monovalent Subunit Influenza Virus Vaccine in Healthy Subjects Aged 18 to 60 Years
Verified date | May 2012 |
Source | Opera Srl |
Contact | n/a |
Is FDA regulated | No |
Health authority | Italy: The Italian Medicines Agency |
Study type | Interventional |
The purpose of this study is explore the antibody and cell mediated immune responses to one injection of Focetria™ pandemic influenza vaccine in healthy adults aged 18-60 years.
Status | Completed |
Enrollment | 7 |
Est. completion date | November 2010 |
Est. primary completion date | November 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Written informed consent obtained; - Males and females from 18 years to 60 years of age on the day of enrolment; - Subjects in good health as determined by the outcome of medical history, physical assessment and clinical judgment by the Investigator; - Subjects are able to comply with all study procedures and are available for all clinic visits scheduled in the study; - Willingness to allow for blood samples to be stored beyond the study period, for potential additional future testing to better characterize immune response. Exclusion Criteria: - Subjects who are not able to comprehend and to follow all required study procedures for the whole period of the study; - Subjects with history or any illness that, in the opinion of the Investigator, might interfere with the results of the study or pose additional risk to the subjects due to participation in the study; - Subjects with any serious chronic or progressive disease according to judgment of the Investigator (including, but not limited to malignant neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease); - History of any anaphylaxis, serious vaccine reactions, or hypersensitivity to influenza viral proteins, to any excipients, and to eggs (including ovalbumin), and chicken proteins; - Subjects who have had seasonal influenza vaccine or documented confirmed seasonal influenza disease within 2 weeks prior to Day 1; - Receipt of another investigational agent within 4 weeks prior to enrolment, or before completion of the safety follow-up period in this or in another study; subjects unwilling to refuse participation in another clinical study throughout the end of this study; - Subjects who received any other vaccines within 4 weeks prior to enrolment in this study or who are planning to receive any vaccine within 4 weeks from the study vaccines; the only exception being plain seasonal influenza vaccines which are allowed until 2 weeks before and over 2 weeks after the study vaccination; - Subjects who have received blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation in the past 12 weeks or plan to receive these products during the full length of the study; - Subjects with axillary temperature = 38°C (= 100.4°F) or oral temperature = 38.5°C (= 101.3°F) within 3 days of intended study vaccination; - Known or suspected impairment/alteration of immune function, for example resulting from: 1. receipt of immunosuppressive therapy such as systemic corticosteroids known to be associated with the suppression of hypothalamic-pituitary-adrenal (HPA) axis (10 mg/day of prednisone or its equivalent) or chronic use of inhaled high-potency corticosteroids (e.g. budesonide 800µg/day or fluticasone 750µg/day) within 60 days prior to Visit 1, 2. cancer chemotherapy within 5 years, 3. receipt of immunostimulants within 60 days prior to Visit 1, 4. history of HIV infection or HIV-related disease; - History of progressive or severe neurological disorders (including Guillain-Barré syndrome and convulsions, but excluding febrile convulsions); - History of or clinically suspected developmental delay; - Bleeding diathesis; - Surgery planned during the study period that in the Investigator's opinion would interfere with the study; - Female subjects who are pregnant or nursing (breastfeeding) mothers, or females of childbearing potential who are sexually active and have not used any of the "acceptable contraceptive methods" for the 2 months before entering the study or do not plan to use them up to the end of the study; - Members of the research staff who have direct access to any study documents containing subject information. |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
Italy | Azienda Ospedaliera Universtaria Senese | Siena |
Lead Sponsor | Collaborator |
---|---|
Opera Srl |
Italy,
Faenzi E, Zedda L, Bardelli M, Spensieri F, Borgogni E, Volpini G, Buricchi F, Pasini FL, Capecchi PL, Montanaro F, Belli R, Lattanzi M, Piccirella S, Montomoli E, Ahmed SS, Rappuoli R, Del Giudice G, Finco O, Castellino F, Galli G. One dose of an MF59-ad — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Antibody and cell mediated immune responses to one 0.50 mL IM injection of egg-derived Focetria™ pandemic influenza vaccine in terms of quality and quantity of the antigen-specific T- and B-cell response | Cell Mediated Immunity (CMI) assessed by frequencies and fold increases of antigen-specific CD4+ T-cells and B-lymphocytes on Day 0,8,22,202. Immunogenicity, i.e. Haemagglutination Inhibition (HI), Single Radial Haemolysis (SRH) and Microneutralization (MN), assessed as follows: Geometric mean titer (GMT)/Geometric mean area (GMA) on Day 0,8,22,202. Geometric mean ratio (GMR) at each time-point vs. Day 0. Percentage of subjects achieving seroconversion or significant increase on Day 8,22,202. Percentage of subjects with HI (or MN) titer=40 and SRH=25 mm2 on Day 0,8,22,202. |
On day 8, 22, 202 after vaccination | No |
Secondary | Antibody responses to one injection of egg-derived Focetria™ pandemic influenza vaccine according to CHMP criteria | In the interpretation of HI immunogenicity results, the following Committee for Medicinal Products for Human Use (CHMP) criteria (CPMP/BWP/214/96) for healthy adults will be taken in consideration: The proportion of subjects achieving seroconversion or significant increase in HI antibody titer should be > 40% Mean geometric increase should be > 2.5 The proportion of subjects achieving an HI titer = 40 should be > 70%. |
On day 8, 22, 202 after vaccination | No |
Secondary | Safety and tolerability | A medical history will be obtained and physical assessment performed for each subject entered into the study at the time of enrolment and then, a brief physical assessment after every subsequent visit. All subjects will be followed for safety throughout the study. All serious adverse events and all adverse events will be collected throughout the entire trial using diary cards. | Within 30 minutes after vaccination (Day 0) and on day 8, 22 and 202 after vaccination | Yes |
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