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    Summary
    EudraCT Number:2010-020069-26
    Sponsor's Protocol Code Number:DMD114044
    National Competent Authority:France - ANSM
    Clinical Trial Type:EEA CTA
    Trial Status:Completed
    Date on which this record was first entered in the EudraCT database:2010-07-15
    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 ConcernedFrance - ANSM
    A.2EudraCT number2010-020069-26
    A.3Full title of the trial
    A randomized, double-blind, placebo-controlled clinical study to assess the efficacy and safety of GSK2402968 in ambulant subjects with Duchenne muscular dystrophy
    A.4.1Sponsor's protocol code numberDMD114044
    A.7Trial is part of a Paediatric Investigation Plan Information not present in EudraCT
    A.8EMA Decision number of Paediatric Investigation Plan
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorGlaxoSmithKline Research and Development LTD
    B.1.3.4CountryUnited Kingdom
    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 support
    B.4.2Country
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisation
    B.5.2Functional name of contact point
    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 Yes
    D.2.5.1Orphan drug designation numberEU/3/08/599
    D.3 Description of the IMP
    D.3.2Product code GSK2402968
    D.3.4Pharmaceutical form 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.3.9.2Current sponsor codeGSK2402968
    D.3.10 Strength
    D.3.10.1Concentration unit mg/ml milligram(s)/millilitre
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number200
    D.3.11 The IMP contains an:
    D.3.11.1Active substance of chemical origin Yes
    D.3.11.2Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP) No
    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 Information not present in EudraCT
    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 placeboInjection*
    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
    Duchenne muscular dystrophy
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 12.1
    E.1.2Level LLT
    E.1.2Classification code 10013801
    E.1.2Term Duchenne muscular dystrophy
    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 efficacy of subcutaneous 6 mg/kg GSK2402968 versus placebo
    administered over 48 weeks in ambulant subjects with DMD.
    E.2.2Secondary objectives of the trial
    • To evaluate the safety and tolerability of subcutaneous 6 mg/kg GSK2402968
    versus placebo administered over 48 weeks in ambulant subjects with DMD.
    • To evaluate the PK of subcutaneous 6 mg/kg GSK2402968 administered over 48
    weeks in ambulant subjects with DMD.
    • To evaluate the impact on quality of life of GSK2402968 administered over 48
    weeks in ambulant subjects with DMD.
    E.2.3Trial contains a sub-study No
    E.3Principal inclusion criteria
    1. Ambulant subjects with Duchenne muscular dystrophy resulting from a
    mutation/deletion within the DMD gene, confirmed by a state-of-the-art DNA
    diagnostic technique covering all DMD gene exons, including but not limited to
    MLPA (Multiplex Ligation-dependent Probe Amplification), CGH (Comparative
    Genomic Hybridisation), SCAIP (Single Condition Amplification/Internal
    Primer) or H-RMCA (High-Resolution Melting Curve Analysis), and correctable
    by GSK2402968-induced DMD exon 51 skipping.

    2. Males, aged at least 5 years,

    3. Life expectancy of at least 1 year,

    4. Able to complete 6MWD test with minimal distance of at least 75m at each predrug
    visit. In addition, results of 6MWD must be within 20% of each other at each
    pre-drug visit.

    5. Receiving glucocorticoids for a minimum of 6 months immediately prior to
    screening, with no significant change in total daily dosage or dosing regimen for a
    minimum of 3 months immediately prior to screening and a reasonable
    expectation that total daily dosage and dosing regimen will not change
    significantly for the duration of the study,

    6. QTc <450msec (based on single or average QTc value of triplicate ECGs obtained
    over a brief recording period), or <480 msec for subjects with Bundle Branch
    Block. Note: QTc may be either QTcB or QTcF, and machine read or manual
    overread.

    7. Subjects, where appropriate, must be willing to use adequate contraception
    (condoms or abstinence) for the duration of the study and for at least 5 months
    after the last dose of study drug.

    8. Willing and able to comply with all protocol requirements and procedures,

    9. Able to give informed assent and/or consent in writing signed by the subject
    and/or parent(s)/legal guardian (according to local regulations).

    10. French subjects: In France, a subject will be eligible for inclusion in this study
    only if either affiliated to or a beneficiary of a social security category.
    E.4Principal exclusion criteria
    1. Any additional missing exon for DMD that cannot be treated with GSK2402968

    2. Current or history of liver or renal disease or impairment

    3. Acute illness within 4 weeks of the first anticipated administration of study
    medication which may interfere with study assessments

    4. Use of anticoagulants, antithrombotics or antiplatelet agents, previous treatment
    with investigational drugs, within 6 months of the first administration of study
    medication; and idebenone or other forms of Coenzyme Q10 within 1 month of
    the first administration of study medication.

    5. Current or anticipated participation in any investigational clinical studies

    6. Positive hepatitis B surface antigen, hepatitis C antibody test (if verified via RIBA
    or PCA testing), or human immunodeficiency virus (HIV) test at screening,

    7. Symptomatic cardiomyopathy. If subject has a left ventricular ejection fraction
    <45% at Screening, the investigator should discuss inclusion of subject in the
    study with the medical monitor,

    8. Children in Care. The definition of a Child in Care is a child who has been placed
    under the control or protection of an agency, organisation, institution or entity by
    the courts, the government or a government body, acting in accordance with
    powers conferred on them by law or regulation. The definition of a child in care
    can include a child cared for by foster parents or living in a care home or
    institution, provided that the arrangement falls within the definition above. The
    definition of a child in care does not include a child who is adopted or has an
    appointed legal guardian.

    NOTE: Subjects who fail on an entry criterion may be allowed to be re-screened at a
    later date, following discussion with the GSK medical monitor.
    E.5 End points
    E.5.1Primary end point(s)
    The primary endpoint is the mean change from baseline in the 6MWD and results will be compared between active and placebo groups using statistical hypothesis testing.
    The primary time point of interest will be the end of treatment (Week 48). Confirmatorystatistical testing will be performed only for the primary variable analysed using the ITT analysis population, therefore, no adjustments for multiplicity are required. A 5% significance level will be used to determine a statistically significant difference.
    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 No
    E.6.8Bioequivalence No
    E.6.9Dose response No
    E.6.10Pharmacogenetic Yes
    E.6.11Pharmacogenomic No
    E.6.12Pharmacoeconomic No
    E.6.13Others No
    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 No
    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 Yes
    E.8.1.1Randomised Yes
    E.8.1.2Open No
    E.8.1.3Single blind No
    E.8.1.4Double blind Yes
    E.8.1.5Parallel group Yes
    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) No
    E.8.2.2Placebo Yes
    E.8.2.3Other No
    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.8.4.1Number of sites anticipated in Member State concerned3
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA11
    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 Information not present in EudraCT
    E.8.6.3If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned
    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
    Last subject last visit
    E.8.9 Initial estimate of the duration of the trial
    E.8.9.1In the Member State concerned years1
    E.8.9.1In the Member State concerned months7
    E.8.9.1In the Member State concerned days22
    E.8.9.2In all countries concerned by the trial years1
    E.8.9.2In all countries concerned by the trial months7
    E.8.9.2In all countries concerned by the trial days22
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 Yes
    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.1.1.6Adolescents (12-17 years) Yes
    F.1.2Adults (18-64 years) No
    F.1.3Elderly (>=65 years) No
    F.2 Gender
    F.2.1Female No
    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 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
    Able to give informed assent and/or consent in writing signed by the subject and/or parent(s)/legal guardian (according to local regulations).
    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 48
    F.4.2.2In the whole clinical trial 180
    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)
    At the end of the study, subjects who complete may be eligible for an open-label extension study following discussion with the Investigator and Medical Monitor. A completed subject is defined as one who has completed 48 weeks of dosing including, as a minimum, efficacy assessments at baseline and at Week 48. Subjects who withdraw from the study for any reason will not be eligible for the extension study.
    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 Decision2010-09-03
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2010-09-16
    P. End of Trial
    P.End of Trial StatusCompleted
    P.Date of the global end of the trial2013-08-28
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