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    Summary
    EudraCT Number:2008-008008-42
    Sponsor's Protocol Code Number:CACZ885G2301E1
    National Competent Authority:Belgium - FPS Health-DGM
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2009-04-09
    Trial results View 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
    N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED
    P. END OF TRIAL
    Expand All   Collapse All
    A. Protocol Information
    A.1Member State ConcernedBelgium - FPS Health-DGM
    A.2EudraCT number2008-008008-42
    A.3Full title of the trial
    An open-label extension study of canakinumab (ACZ885) in patients with Systemic Juvenile Idiopathic Arthritis (SJIA) and active systemic manifestations WHO PARTICIPATED IN STUDIES ACZ885G2301 AND
    ACZ885G2305;AND RESPONSE CHARACTERIZATION STUDY IN CANAKINUMAB TREATMENT-NAÏVE PATIENTS WITH ACTIVE SJIA WITH AND WITHOUT FEVER
    A.3.2Name or abbreviated title of the trial where available
    G2301E1
    A.4.1Sponsor's protocol code numberCACZ885G2301E1
    A.7Trial is part of a Paediatric Investigation Plan Yes
    A.8EMA Decision number of Paediatric Investigation PlanP/296/2011
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorNovartis Pharma Services AG
    B.1.3.4CountrySwitzerland
    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 supportNovartis Pharma Services AG
    B.4.2CountrySwitzerland
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationNovartis Pharma Services AG
    B.5.2Functional name of contact pointClinical Trial Information Desk
    B.5.3 Address:
    B.5.3.1Street AddressForum 1, Novartis Campus
    B.5.3.2Town/ cityBasel
    B.5.3.3Post code4056
    B.5.3.4CountryBelgium
    B.5.4Telephone number+41613241111
    B.5.5Fax number+41613248001
    B.5.6E-mailclinicaltrial.enquiries@novartis.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 Yes
    D.2.1.1.1Trade name Ilaris
    D.2.1.1.2Name of the Marketing Authorisation holderNovartis Europharm Ltd
    D.2.1.2Country which granted the Marketing AuthorisationEuropean Union
    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 nameCanakinumab
    D.3.2Product code ACZ885
    D.3.4Pharmaceutical form Powder for solution for injection
    D.3.4.1Specific paediatric formulation Information not present in EudraCT
    D.3.7Routes of administration for this IMPSubcutaneous use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNCANAKINUMAB
    D.3.9.1CAS number 914613-48-2
    D.3.9.2Current sponsor codeACZ885
    D.3.9.4EV Substance CodeSUB30137
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number150
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNCANAKINUMAB
    D.3.9.1CAS number 914613-48-2
    D.3.9.2Current sponsor codeACZ885
    D.3.9.4EV Substance CodeSUB30137
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number25
    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) Information not present in EudraCT
    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 Information not present in EudraCT
    D.3.11.3.4Combination ATIMP (i.e. one involving a medical device) Information not present in EudraCT
    D.3.11.3.5Committee on Advanced therapies (CAT) has issued a classification for this product Information not present in EudraCT
    D.3.11.4Combination product that includes a device, but does not involve an Advanced Therapy Information not present in EudraCT
    D.3.11.5Radiopharmaceutical medicinal product No
    D.3.11.6Immunological medicinal product (such as vaccine, allergen, immune serum) No
    D.3.11.7Plasma derived medicinal product No
    D.3.11.8Extractive medicinal product No
    D.3.11.9Recombinant medicinal product Yes
    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
    D.8 Placebo: 1
    D.8.1Is a Placebo used in this Trial?Yes
    D.8.3Pharmaceutical form of the placeboLyophilisate for solution for injection
    D.8.4Route of administration of the placeboSubcutaneous use
    E. General Information on the Trial
    E.1 Medical condition or disease under investigation
    E.1.1Medical condition(s) being investigated
    Active systemic manifestations of Systemic Juvenile Idiopathic Arthritis (SJIA)
    E.1.1.2Therapeutic area Diseases [C] - Musculoskeletal Diseases [C05]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 14.1
    E.1.2Level LLT
    E.1.2Classification code 10059176
    E.1.2Term Juvenile idiopathic arthritis
    E.1.2System Organ Class 100000004859
    E.1.3Condition being studied is a rare disease Yes
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    •To assess the long-term safety, tolerability, and immunogenicity of
    canakinumab
    •To assess efficacy at an exploratory level by investigating disease
    control defined by maintenance of at least an adapted ACR pediatric 30
    during the extension PHASE
    •To perform biomarker analyses to explore the characteristics of
    response to canakinumab
    treatment
    •To introduce Juvenile Arthritis Disease Activity Score (JADAS) and
    Disease Activity Score
    (DAS) as exploratory assessments of efficacy
    •To assess efficacy of canakinumab treatment based on adapted
    pediatric ACR30 criteria in
    patients who report previous Anakinra, tocilizumab or other biologic
    treatment
    E.2.2Secondary objectives of the trial
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    1.Parent's or legal guardian's written informed consent and child's
    assent, if appropriate, or patient's informed consent for ≥ 18 years of
    age before any study related activity is performed.
    2.The following patients are eligible to participate in the open label
    extension study (CACZ885G2301E1):
    • Patients from study CACZ885G2305 or CACZ885G2301 who achieved
    an adapted ACR pediatric 30 response 15 days after their initial dose of
    canakinumab but clinically deteriorated AS DEFINED BY a minimum ACR
    Pediatric 30 response not BEING maintained after Day 15 and
    intervention is deemed necessary by the investigator.
    • Patients in study CACZ885G2301 who are not eligible to enter Part II
    (withdrawal part) because they were not able to meet the corticosteroid
    entry criteria of 0.5 mg/kg oral prednisone (or equivalent) or were not
    able to taper their steroids by at least 0.3 mg/kg (please refer to
    CACZ885G2301 protocol for detailed rules)
    • Responder patients in Part I or Part II who were maintaining their
    minimum ACR pediatric 30 response or had not flared when
    CACZ885G2301 was stopped.
    • CACZ885G2301 patients who were responders in Part I (achieved and
    maintained a minimum adapted ACR pediatric 30) but experienced a
    flare in Part II.
    • Treatment-naïve patients need to meet the following criteria:
    - Confirmed diagnosis of Systemic Juvenile Idiopathic Arthritis as per
    ILAR definition that must have occured at least 2 months prior to
    enrollment with onset of disease < 16 years of age
    - Male and female patients aged ≥ 2 TO < 20 years of age
    - Active disease at the time of enrollment defined as having 2 or more of
    the following:documented spiking, intermittent fever (body temperature
    >38°C) for at least 1 day during the screening period and within 1 week
    before first canakinumab dose; at least 2 joints with active arthritis; Creactive
    protein (CRP) > 30 mg/l (normal range < 10 MG/L); rash;
    serositis; lymphadenopathy and hepatosplenomegaly
    - Naïve to canakinumab
    OTHER PROTOCOL-DEFINED INCLUSION CRITERIA MAY APPLY
    E.4Principal exclusion criteria
    1. Pregnant or nursing (lactating) female patients
    2. Female patients having reached sexual maturity UNLESS they are:
    • female patients whose career, lifestyle, or sexual orientation precludes
    intercourse with a male partner and/or
    • using an acceptable method of contraception with a failure rate (Pearl
    Index (PI)) < 1.
    Reliable contraception should be maintained throughout the study and
    for 3 months after study drug discontinuation.
    3. History hypersensitivity to study drug or to biologics.
    4. With active or recurrent bacterial, fungal or viral infection at the time
    of enrollment
    5. Risk factors for tuberculosis (TB)
    6. With underlying metabolic, renal, hepatic, infectious or
    gastrointestinal conditions which in the opinion of the investigator
    immunocompromises the patient and/ or places the patient at
    unacceptable risk for participation in an immunodulatory therapy. In
    particular, clinical evidence or history of multiple sclerosis or other
    demyelinating diseases, or Felty's syndrome
    7. With neutropenia (absolute neutrophil count <1500/mm3) at
    screening
    8. With significant medical conditions, which in the opinion of the
    Investigator will exclude the patient from the study (can be discussed on
    a case by case basis with Novartis)
    9. History of malignancy of any organ system (other than localized basal
    cell carcinoma of the skin), treated or untreated, within the past 5 years,
    regardless of whether there is evidence of local recurrence or
    metastases
    10. Live vaccinations within 3 months prior to the start of the study.
    Killed or inactivated vaccines may be permitted according to the
    investigator's discretion.
    11. Donation or loss of blood (amount depending on age and weight, 10-
    20% or more of volume, see Appendix 3 within 8 weeks prior to first
    dosing, or longer if required by local regulation.
    12. Familial and social conditions rendering regular medical assessment
    not possible
    13. History of drug or alcohol abuse within the 12 months prior to
    dosing.
    No additional exclusions may be applied by the investigator, in order to
    ensure that the study population will be representative of all eligible
    patients.
    OTHER PROTOCOL-DEFINED INCLUSION/EXCLUSION CRITERIA MAY
    APPLY.
    E.5 End points
    E.5.1Primary end point(s)
    - Long-term safety, tolerability, and immunogenicity of canakinumab
    - Disease control by maintenance of at least an adapted ACR pediatric 30
    - Assess efficacy of canakinumab treatment based based on adapted ACR
    Paediatric 30 criteria in patients who report previous anakinra,
    tocilizumab or other biologic treatment
    E.5.1.1Timepoint(s) of evaluation of this end point
    DAYS 1 TO 728
    E.5.2Secondary end point(s)
    1) The number of patients that were able to taper steroid as per
    protocol.
    2) The number of patients who reached steroid free regimen
    3) The number of patients who were able to reduce the canakinumab
    dose to 2 mg/kg/4 week
    4) The percentage of patients who will meet the definition of inactive
    disease on medication and possible clinical remission on medication
    E.5.2.1Timepoint(s) of evaluation of this end point
    DAYS 1 TO 728
    E.6 and E.7 Scope of the trial
    E.6Scope of the trial
    E.6.1Diagnosis No
    E.6.2Prophylaxis No
    E.6.3Therapy Yes
    E.6.4Safety Yes
    E.6.5Efficacy Yes
    E.6.6Pharmacokinetic Yes
    E.6.7Pharmacodynamic Yes
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic Yes
    E.6.11Pharmacogenomic Yes
    E.6.12Pharmacoeconomic No
    E.6.13Others Yes
    E.6.13.1Other scope of the trial description
    tolerability and immunogenicity
    E.7Trial type and phase
    E.7.1Human pharmacology (Phase I) No
    E.7.1.1First administration to humans Information not present in EudraCT
    E.7.1.2Bioequivalence study Information not present in EudraCT
    E.7.1.3Other Information not present in EudraCT
    E.7.1.3.1Other trial type description
    E.7.2Therapeutic exploratory (Phase II) No
    E.7.3Therapeutic confirmatory (Phase III) Yes
    E.7.4Therapeutic use (Phase IV) No
    E.8 Design of the trial
    E.8.1Controlled No
    E.8.1.1Randomised No
    E.8.1.2Open Yes
    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 No
    E.8.2 Comparator of controlled trial
    E.8.2.1Other medicinal product(s) Information not present in EudraCT
    E.8.2.2Placebo Information not present in EudraCT
    E.8.2.3Other 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.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA48
    E.8.6 Trial involving sites outside the EEA
    E.8.6.1Trial being conducted both within and outside the EEA Yes
    E.8.6.2Trial being conducted completely outside of the EEA No
    E.8.6.3If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned
    Argentina
    Austria
    Belgium
    Brazil
    Canada
    France
    Germany
    Greece
    Hungary
    Israel
    Italy
    Netherlands
    Peru
    Poland
    Russian Federation
    Spain
    Sweden
    Switzerland
    Turkey
    United Kingdom
    United States
    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
    LVLS
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years4
    E.8.9.1In the Member State concerned months9
    E.8.9.1In the Member State concerned days
    E.8.9.2In all countries concerned by the trial years4
    E.8.9.2In all countries concerned by the trial months9
    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: 205
    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) No
    F.1.1.5Children (2-11years) Yes
    F.1.1.5.1Number of subjects for this age range: 140
    F.1.1.6Adolescents (12-17 years) Yes
    F.1.1.6.1Number of subjects for this age range: 65
    F.1.2Adults (18-64 years) Yes
    F.1.2.1Number of subjects for this age range: 5
    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 No
    F.3.2Patients Yes
    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 Yes
    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
    Pediatric patients
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.1In the member state
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 123
    F.4.2.2In the whole clinical trial 210
    G. Investigator Networks to be involved in the Trial
    N. Review by the Competent Authority or Ethics Committee in the country concerned
    N.Competent Authority Decision Authorised
    N.Date of Competent Authority Decision2009-05-04
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2009-06-04
    P. End of Trial
    P.End of Trial StatusCompleted
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
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