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    Summary
    EudraCT Number:2009-013105-34
    Sponsor's Protocol Code Number:810706
    Clinical Trial Type:Outside EU/EEA
    Date on which this record was first entered in the EudraCT database:2011-04-05
    Trial results
    Index
    A. PROTOCOL INFORMATION
    B. SPONSOR INFORMATION
    C. APPLICANT IDENTIFICATION
    D. IMP IDENTIFICATION
    D.8 INFORMATION ON PLACEBO
    E. GENERAL INFORMATION ON THE TRIAL
    F. POPULATION OF TRIAL SUBJECTS
    G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL
    H.4 THIRD COUNTRY IN WHICH THE TRIAL WAS FIRST AUTHORISED
    Expand All   Collapse All
    A. Protocol Information
    A.2EudraCT number2009-013105-34
    A.3Full title of the trial
    A PHASE I/II STUDY TO ASSESS THE SAFETY AND IMMUNOGENICITY OF A VERO CELL-DERIVED WHOLE VIRUS H5N1 INFLUENZA VACCINE IN HEALTHY INFANTS, CHILDREN AND ADOLESCENTS AGED 6 MONTHS TO 17 YEARS
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    A clinical study to assess safety of and immune response to a whole virus H5N1 bird flu vaccine in children aged 6 months to 17 years
    A.3.2Name or abbreviated title of the trial where available
    Phase I/II Study of a H5N1 Vaccine in the Pediatric Population
    A.4.1Sponsor's protocol code number810706
    A.7Trial is part of a Paediatric Investigation Plan Yes
    A.8EMA Decision number of Paediatric Investigation PlanP/67/2011
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorBaxter Innovations GmbH
    B.1.3.4CountryAustria
    B.3.1 and B.3.2Status of the sponsorCommercial
    B.4 Source(s) of Monetary or Material Support for the clinical trial:
    B.4.1Name of organisation providing supportBaxter Innovations GmbH
    B.4.2CountryAustria
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationDr Guido Wuerth
    B.5.2Functional name of contact pointCl Develoment and Medical Services
    B.5.3 Address:
    B.5.3.1Street AddressWagramer Strasse 17-19
    B.5.3.2Town/ cityVienna
    B.5.3.3Post code1220
    B.5.3.4CountryAustria
    B.5.4Telephone number+431201003489
    B.5.5Fax number+43120100717
    B.5.6E-mailguido_wuerth@baxter.com
    D. IMP Identification
    D.IMP: 1
    D.1.2 and D.1.3IMP RoleTest
    D.2 Status of the IMP to be used in the clinical trial
    D.2.1IMP to be used in the trial has a marketing authorisation No
    D.2.5The IMP has been designated in this indication as an orphan drug in the Community No
    D.2.5.1Orphan drug designation number
    D.3 Description of the IMP
    D.3.1Product nameVero Cell-Derived Whole Virus H5N1
    D.3.2Product code H5N1 Influenza Vaccine
    D.3.4Pharmaceutical form Solution for injection
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPIntramuscular use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNWhole virion non-adjuvanted influenza virus, propagated in Vero cells, inactivated,
    D.3.10 Strength
    D.3.10.1Concentration unit µg/ml microgram(s)/millilitre
    D.3.10.2Concentration typenot less then
    D.3.10.3Concentration number15
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin No
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) Yes
    The IMP is a:
    D.3.11.3Advanced Therapy IMP (ATIMP) No
    D.3.11.3.1Somatic cell therapy medicinal product No
    D.3.11.3.2Gene therapy medical product No
    D.3.11.3.3Tissue Engineered Product No
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) No
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product No
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy No
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) Yes
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product No
    D.3.11.10Medicinal product containing genetically modified organisms No
    D.3.11.11Herbal medicinal product No
    D.3.11.12Homeopathic medicinal product No
    D.3.11.13Another type of medicinal product No
    D.8 Information on Placebo
    E. General Information on the Trial
    E.1 Medical condition or disease under investigation
    E.1.1Medical condition(s) being investigated
    Prophylaxis of influenza infection caused by a pandemic influenza virus
    (H5N1)
    E.1.1.1Medical condition in easily understood language
    Prevention of influenza infection caused by a pandemic influenza virus
    (bird flu)
    E.1.1.2Therapeutic area Diseases [C] - Virus Diseases [C02]
    MedDRA Classification
    E.1.3Condition being studied is a rare disease No
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    To assess safety: Frequency and severity of systemic reactions until 7
    days after the first vaccination.
    To assess immunogenicity: Rate of subjects with antibody response to
    the vaccine strain associated with protection 21 days after the second
    vaccination defined as titer measured by Microneutralization (MN) test
    >= 1:20.
    E.2.2Secondary objectives of the trial
    To assess the safety and tolerability of a non-adjuvanted H5N1 influenza
    vaccine in healthy infants, children and adolescents aged 6 months to 17
    years;
    Rate of subjects with antibody response 21 days after the first and
    second vaccination ; Fold increase of antibody response 21 days after
    the first and second vaccination as compared to baseline; Rate of
    subjects with seroconversion 21 days after the first, second and booster
    vaccination; Rate of subjects with antibody response associated with
    protection 360 days after the first vaccination and 21 days after the
    booster vaccination; Antibody response 360 days after the first
    vaccination and 21 days after the booster vaccination; Fold increase of
    antibody response 21 days after the booster vaccination as compared to
    before the booster;
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    Male and female subjects will be eligible for participation in this study if:
    • They are 9 to 17ii years of age on the day of screening (for Stratum A
    only);
    • They are 3 to 8iii years of age on the day of screening (for Stratum B
    onl
    • They are 6 to 35iv months of age on the day of screening (for Stratum
    C only);
    • They were born at full term of pregnancy (≥ 37 weeks) with a birth
    weight ≥ 2 kg (for Stratum C only);
    • They and/or their parents/legal guardians understand the nature and
    procedures of the study and agree to its provisions;
    • Their parents/legal guardians provide written consent for participation
    according to national law. In case the parents/legal guardians are
    illiterate, the informed consent is also to be signed by an independent
    witness;
    • They provide written assent according to their age and capacity of
    understanding;
    • They are generally healthy, as determined by the investigator's clinical
    judgment through collection of medical history and performance of a
    physical examination;
    • They are physically and mentally capable of participating in the study
    and follow its procedures;
    • They and/or their parents/legal guardians agree to keep a daily record
    of symptoms for the duration of the study;
    • If female of childbearing potential – have a negative urine pregnancy
    test result within 24 hours prior to the scheduled first vaccination and
    agree to employ adequate birth control measures for the duration of the
    study.
    ii From the 9th birthday to the last day before the 18th birthday
    iii From the 3rd birthday to the last day before the 9th birthday
    iv From 6 months of age to the last day before the 3rd birthday
    E.4Principal exclusion criteria
    Subjects will be excluded from participation in this study if:
    • They have a history of exposure to H5N1 virus or a history of
    vaccination with an H5N1 influenza vaccine;
    • They are at high risk of contracting H5N1 influenza infection (e.g.
    contact with poultry);
    • They currently have or have a history of a significant neurological,
    cardiovascular, pulmonary (including asthma), hepatic, metabolic,
    rheumatic, autoimmune, hematological or renal disorderv;
    • They have any inherited or acquired immunodeficiency;
    • They have a disease or are currently undergoing a form of treatment or
    were undergoing a form of treatment within 30 days prior to study entry
    that can be expected to influence immune response. Such treatment
    includes, but is not limited to, systemic or high dose inhaled
    corticosteroids, radiation treatment or other immunosuppressive or
    cytotoxic drugs;
    • They have a history of severe allergic reactions or anaphylaxis;
    • They have a rash, dermatological condition or tattoos which may
    interfere with injection site reaction rating;
    • They have received a blood transfusion or immunoglobulins or other
    derivatives within 90 days prior to study entry;
    • They have received any live vaccine within 4 weeks or inactivated
    vaccine within 2 weeks prior to vaccination in this study;
    • They have a functional or surgical asplenia;
    • They have a known or suspected problem with alcohol or drug abuse;
    • They were administered an investigational drug within 6 weeks prior
    to study entry or are concurrently participating in a clinical study that
    includes the administration of an investigational product;
    • They are in a dependent relationship with the study site personnel.
    Dependent relationships include close relatives (i.e., children, siblings);
    • If female: are pregnant or lactating.
    E.5 End points
    E.5.1Primary end point(s)
    Safety:
    • Frequency and severity of systemic reactions until 7 days after the first and second vaccination.
    Immunogenicity:
    • Rate of subjects with antibody response to the vaccine strain
    associated with protection 21 days after the second vaccination defined
    as titer measured by Microneutralization (MN) test ≥ 1:20.
    E.5.1.1Timepoint(s) of evaluation of this end point
    see E.5.1
    E.5.2Secondary end point(s)
    Safety:
    • Frequency and severity of systemic reactions until 21 days after the
    first, second and booster vaccination;
    • Frequency and severity of injection site reactions until 21 days after
    the first, second and booster vaccination;
    • Rate of subjects with fever, malaise or shivering (in children and
    adolescents aged 3 to 17 years) and fever and irritability (in infants and
    young children aged 6 to 35 months) with onset within 7 days after the
    first, second and booster vaccination;
    • Frequency and severity of adverse events (AEs) observed during the
    entire study period.
    Immunogenicity:
    • Rate of subjects with antibody response associated with protection 21
    days after the first and second vaccination defined as Hemagglutination
    Inhibition Antibody (HIA) titer
    ≥ 1:40 or Single Radial Hemolysis (SRH) area ≥25 mm2;
    • Rate of subjects with antibody response associated with protection 21
    days after the first vaccination defined as titer measured by MN test ≥
    1:20;
    • Antibody response 21 days after the first and second vaccination as
    measured by MN, HI and SRH assay;
    • Fold increase of antibody response 21 days after the first and second
    vaccination as compared to baseline as measured by MN, HI and SRH
    assay;
    • Rate of subjects with seroconversion (defined as a minimum four fold
    titer increase as compared to baseline [for MN and HI assay] or as either
    a ≥ 25 mm2 hemolysis area after the vaccination in case of a negative
    prevaccination sample [≤ 4 mm2] or a ≥50% increase in
    hemolysis area if the pre-vaccination sample is > 4 mm2 [for SRH
    assay]) 21 days after the first and second vaccination as measured by
    MN, HI and SRH assay;
    • Rate of subjects with antibody response associated with protection
    360 days after the first vaccination and 21 days after the booster
    vaccination as measured by MN, HI and SRH assay;
    • Antibody response 360 days after the first vaccination and 21 days
    after the booster vaccination as measured by MN, HI and SRH assay;
    • Fold increase of antibody response 21 days after the booster
    vaccination as compared to before the booster vaccination as measured
    by MN, HI and SRH assay;
    • Rate of subjects with seroconversion 21 days after the booster
    vaccination as measured by MN, HI and SRH assay.
    E.5.2.1Timepoint(s) of evaluation of this end point
    see E.5.2
    E.6 and E.7 Scope of the trial
    E.6Scope of the trial
    E.6.1Diagnosis No
    E.6.2Prophylaxis Yes
    E.6.3Therapy No
    E.6.4Safety Yes
    E.6.5Efficacy No
    E.6.6Pharmacokinetic No
    E.6.7Pharmacodynamic No
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic No
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic No
    E.6.13Others Yes
    E.6.13.1Other scope of the trial description
    Immunogenicity
    E.7Trial type and phase
    E.7.1Human pharmacology (Phase I) No
    E.7.1.1First administration to humans No
    E.7.1.2Bioequivalence study No
    E.7.1.3Other Yes
    E.7.1.3.1Other trial type description
    Phase I/II Study of a H5N1 vaccine
    E.7.2Therapeutic exploratory (Phase II) Yes
    E.7.3Therapeutic confirmatory (Phase III) No
    E.7.4Therapeutic use (Phase IV) No
    E.8 Design of the trial
    E.8.1Controlled Yes
    E.8.1.1Randomised Yes
    E.8.1.2Open No
    E.8.1.3Single blind No
    E.8.1.4Double blind No
    E.8.1.5Parallel group No
    E.8.1.6Cross over No
    E.8.1.7Other Yes
    E.8.1.7.1Other trial design description
    Partially blinded phase I/II clinical study
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) No
    E.8.2.2Placebo No
    E.8.2.3Other Yes
    E.8.2.3.1Comparator description
    randomized into dose groups
    E.8.2.4Number of treatment arms in the trial2
    E.8.3 Will this trial be conducted at a single site globally? No
    E.8.4 Will this trial be conducted at multiple sites globally? Yes
    E.8.6 Trial involving sites outside the EEA
    E.8.6.2Trial being conducted completely outside of the EEA No
    E.8.6.3Specify the countries outside of the EEA in which trial sites are planned
    Australia
    Singapore
    E.8.7Trial has a data monitoring committee Yes
    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
    This study is terminated when the last subject completes day 381 (Visit 8).The study may be prematurely terminated if SAEs or other
    significant vaccine related side effects occur. In addition the Sponsor
    may stop the entire study for any medical reason at any time.
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.2In all countries concerned by the trial years2
    E.8.9.2In all countries concerned by the trial months8
    E.8.9.2In all countries concerned by the trial days0
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 Yes
    F.1.1Number of subjects for this age range: 670
    F.1.1.1In Utero No
    F.1.1.2Preterm newborn infants (up to gestational age < 37 weeks) No
    F.1.1.3Newborns (0-27 days) No
    F.1.1.4Infants and toddlers (28 days-23 months) Yes
    F.1.1.5Children (2-11years) Yes
    F.1.1.6Adolescents (12-17 years) Yes
    F.1.2Adults (18-64 years) No
    F.1.3Elderly (>=65 years) No
    F.2 Gender
    F.2.1Female Yes
    F.2.2Male Yes
    F.3 Group of trial subjects
    F.3.1Healthy volunteers Yes
    F.3.2Patients No
    F.3.3Specific vulnerable populations Yes
    F.3.3.1Women of childbearing potential not using contraception No
    F.3.3.2Women of child-bearing potential using contraception No
    F.3.3.3Pregnant women No
    F.3.3.4Nursing women No
    F.3.3.5Emergency situation No
    F.3.3.6Subjects incapable of giving consent personally Yes
    F.3.3.6.1Details of subjects incapable of giving consent
    subjects are not of legal age
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.2 For a multinational trial
    F.4.2.2In the whole clinical trial 670
    F.5 Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)
    Prophylactic vaccine; no treatment needed after participation in the
    trial
    G. Investigator Networks to be involved in the Trial
    H.4 Third Country in which the Trial was first authorised
    H.4.1Third Country in which the trial was first authorised: Australia
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