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    Summary
    EudraCT Number:2013-000743-33
    Sponsor's Protocol Code Number:SPD602-204
    National Competent Authority:Greece - EOF
    Clinical Trial Type:EEA CTA
    Trial Status:Prematurely Ended
    Date on which this record was first entered in the EudraCT database:2013-11-25
    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 ConcernedGreece - EOF
    A.2EudraCT number2013-000743-33
    A.3Full title of the trial
    A 48-week, Open-label, 2-arm, Parallel-group, Randomized Exploratory Study to Assess Liver Iron Concentration Measured by FerriScan® (R2) Magnetic Resonance Imaging in β-thalassemia Subjects Administered SPD602 (SSP-004184AQ) or Exjade® (deferasirox) for Treatment of Chronic Transfusional Iron Overload
    Mία ανοικτή, τυχαιοποιημένη, διερευνητική κλινική μελέτη παραλλήλων ομάδων ασθενών, δύο θεραπευτικών σκελών, διάρκειας 48 εβδομάδων για την αξιολόγηση των ηπατικών συγκεντρώσεων σιδήρου, μετρουμένων μέσω μαγνητικής τομογραφίας FerriScan (R2) σε ασθενείς με β-θαλασσαιμία οι οποίοι λαμβάνουν SPD602 (SSP-004184AQ) ή Exjade (deferasirox) για τη θεραπεία της χρόνιας υπερσιδήρωσης λόγω μεταγγίσεων.
    A.3.1Title of the trial for lay people, in easily understood, i.e. non-technical, language
    Treatment of Iron Overload Requiring Chelation Therapy
    Θεραπεία ασθενών με β-θαλασσαιμία με υπερφόρτωση σιδήρου λόγω μεταγγίσεων, οι οποίοι απαιτούν θεραπεία με χηλικούς παράγοντες
    A.4.1Sponsor's protocol code numberSPD602-204
    A.7Trial is part of a Paediatric Investigation Plan No
    A.8EMA Decision number of Paediatric Investigation Plan
    B. Sponsor Information
    B.Sponsor: 1
    B.1.1Name of SponsorShire Development LLC and International Affiliates
    B.1.3.4CountryUnited States
    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 supportShire Development LLC and International Affiliates
    B.4.2CountryUnited States
    B.5 Contact point designated by the sponsor for further information on the trial
    B.5.1Name of organisationShire Development LLC and International Affiliates
    B.5.2Functional name of contact pointBjorn Mellgard
    B.5.3 Address:
    B.5.3.1Street Address725 Chesterbrook Boulevard
    B.5.3.2Town/ cityWayne, PA
    B.5.3.3Post code19087
    B.5.3.4CountryUnited States
    B.5.4Telephone number+41224194110
    B.5.6E-mailbmellgard@shire.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 Yes
    D.2.5.1Orphan drug designation numberEU/3/09/647
    D.3 Description of the IMP
    D.3.1Product nameSSP-004184AQ 50 mg Capsule
    D.3.2Product code SSP-004184AQ 50 mg
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot Assigned
    D.3.9.1CAS number 1173095-59-5
    D.3.9.2Current sponsor codeSSP-004184AQ
    D.3.9.3Other descriptive name(S)-4,5-dihydro-2[hydroxy-3-(3,6,9-trioxadecyloxy)phenyl]-4-methyl-4-thiazolecarboxylate magnesium hydroxide
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number50
    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) 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) No
    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.IMP: 2
    D.1.2 and D.1.3IMP RoleComparator
    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 Exjade
    D.2.1.1.2Name of the Marketing Authorisation holderNovartis Europharm Limited
    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 Yes
    D.2.5.1Orphan drug designation numberEU/3/02/092
    D.3 Description of the IMP
    D.3.1Product nameExjade
    D.3.4Pharmaceutical form Dispersible tablet
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNdeferasirox
    D.3.9.1CAS number 201530-41-8
    D.3.9.3Other descriptive name[4-[(3Z,5E)-3,5-bis(6-oxo-1-cyclohexa-2,4-dienylidene)-1,2,4-triazolidin-1-yl]benzoic acid
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number125
    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) 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) No
    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.IMP: 3
    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/3/09/647
    D.3 Description of the IMP
    D.3.1Product nameSSP-004184AQ 100 mg Capsule
    D.3.2Product code SSP-004184AQ 100 mg
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot Assigned
    D.3.9.1CAS number 1173095-59-5
    D.3.9.2Current sponsor codeSSP-004184AQ
    D.3.9.3Other descriptive name(S)-4,5-dihydro-2[hydroxy-3-(3,6,9-trioxadecyloxy)phenyl]-4-methyl-4-thiazolecarboxylate magnesium hydroxide
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number100
    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) 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) No
    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.IMP: 4
    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/3/09/647
    D.3 Description of the IMP
    D.3.1Product nameSSP-004184AQ 200 mg Capsule
    D.3.2Product code SSP-004184AQ 200 mg
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot Assigned
    D.3.9.1CAS number 1173095-59-5
    D.3.9.2Current sponsor codeSSP-004184AQ
    D.3.9.3Other descriptive name(S)-4,5-dihydro-2[hydroxy-3-(3,6,9-trioxadecyloxy)phenyl]-4-methyl-4-thiazolecarboxylate magnesium hydroxide
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    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) 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) No
    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.IMP: 5
    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/3/09/647
    D.3 Description of the IMP
    D.3.1Product nameSSP-004184AQ 375 mg Capsule
    D.3.2Product code SSP-004184AQ 375 mg
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot Assigned
    D.3.9.1CAS number 1173095-59-5
    D.3.9.2Current sponsor codeSSP-004184AQ
    D.3.9.3Other descriptive name(S)-4,5-dihydro-2[hydroxy-3-(3,6,9-trioxadecyloxy)phenyl]-4-methyl-4-thiazolecarboxylate magnesium hydroxide
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number375
    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) 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) No
    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.IMP: 6
    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/3/09/647
    D.3 Description of the IMP
    D.3.1Product nameSSP-004184AQ 500 mg Capsule
    D.3.2Product code SSP-004184AQ 500 mg
    D.3.4Pharmaceutical form Capsule
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNNot Assigned
    D.3.9.1CAS number 1173095-59-5
    D.3.9.2Current sponsor codeSSP-004184AQ
    D.3.9.3Other descriptive name(S)-4,5-dihydro-2[hydroxy-3-(3,6,9-trioxadecyloxy)phenyl]-4-methyl-4-thiazolecarboxylate magnesium hydroxide
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number500
    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) 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) No
    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.IMP: 7
    D.1.2 and D.1.3IMP RoleComparator
    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 Exjade
    D.2.1.1.2Name of the Marketing Authorisation holderNovartis Europharm Limited
    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 Yes
    D.2.5.1Orphan drug designation numberEU/3/02/092
    D.3 Description of the IMP
    D.3.1Product nameExjade
    D.3.4Pharmaceutical form Dispersible tablet
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNdeferasirox
    D.3.9.1CAS number 201530-41-8
    D.3.9.3Other descriptive name[4-[(3Z,5E)-3,5-bis(6-oxo-1-cyclohexa-2,4-dienylidene)-1,2,4-triazolidin-1-yl]benzoic acid
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number250
    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) 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) No
    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.IMP: 8
    D.1.2 and D.1.3IMP RoleComparator
    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 Exjade
    D.2.1.1.2Name of the Marketing Authorisation holderNovartis Europharm Limited
    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 Yes
    D.2.5.1Orphan drug designation numberEU/3/02/092
    D.3 Description of the IMP
    D.3.1Product nameExjade
    D.3.4Pharmaceutical form Dispersible tablet
    D.3.4.1Specific paediatric formulation No
    D.3.7Routes of administration for this IMPOral use
    D.3.8 to D.3.10 IMP Identification Details (Active Substances)
    D.3.8INN - Proposed INNdeferasirox
    D.3.9.1CAS number 201530-41-8
    D.3.9.3Other descriptive name[4-[(3Z,5E)-3,5-bis(6-oxo-1-cyclohexa-2,4-dienylidene)-1,2,4-triazolidin-1-yl]benzoic acid
    D.3.10 Strength
    D.3.10.1Concentration unit mg milligram(s)
    D.3.10.2Concentration typeequal
    D.3.10.3Concentration number500
    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) 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) No
    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
    Patients 18 years of age and older with transfusional iron overload due to β-thalassemia
    Ασθενείς ηλικίας ίσης ή μεγαλύτερης των 18 ετών με υπερφόρτωση σιδήρου λόγω μεταγγίσεων, οφειλόμενη σε β-θαλασσαιμία
    E.1.1.1Medical condition in easily understood language
    Patients with β-thalassemia that have received long-term blood transfusion therapy leading to an overload of iron.
    Ασθενείς με β-θαλασσαιμία, οι οποίοι υποβάλλονται για πολλά χρόνια σε μεταγγίσεις, οι οποίες οδήγησαν σε υπερφόρτωσή τους με σίδηρο
    E.1.1.2Therapeutic area Diseases [C] - Nutritional and Metabolic Diseases [C18]
    MedDRA Classification
    E.1.2 Medical condition or disease under investigation
    E.1.2Version 14.1
    E.1.2Level LLT
    E.1.2Classification code 10065974
    E.1.2Term Chronic iron overload
    E.1.2System Organ Class 100000004861
    E.1.3Condition being studied is a rare disease Yes
    E.2 Objective of the trial
    E.2.1Main objective of the trial
    1. Provide a descriptive assessment of change in LIC from baseline utilizing FerriScan® (R2) MRI in subjects with transfusional iron overload receiving SSP-004184AQ or deferasirox whose primary diagnosis is β-thalassemia.

    2. To evaluate the response rate over time in subjects with transfusional iron overload receiving SSP-004184AQ or deferasirox whose primary diagnosis is β-thalassemia.

    3. To assess the change in CIC measured by T2* MRI from baseline in subjects receiving SSP-004184AQ or deferasirox.

    4. To assess the change in serum ferritin levels from baseline in subjects receiving SSP-004184AQ or deferasirox.

    5. To provide a descriptive assessment of change in LIC from baseline utilizing R2* MRI in subjects with transfusional iron overload receiving SSP-004184AQ or deferasirox whose primary diagnosis is β-Thalassemia.

    6. To provide a descriptive assessment of change in PIC as measured by R2* MRI from baseline in subjects receiving SSP-004184AQ or deferasirox

    1. Αξιολόγηση της μεταβολής του σιδήρου στο ήπαρ (LIC) από τη βασική επίσκεψη, με την τεχνική MRI FerriScan (R2) σε ασθενείς με υπερσιδήρωση από μεταγγίσεις, με SSP-004184AQ ή deferasirox, με κύρια διάγνωση β-θαλασσαιμία.
    2. Αξιολόγηση του ποσοστού ανταπόκρισης προς το χρόνο σε ασθενείς με υπερσιδήρωση από μεταγγίσεις με SSP-004184AQ ή deferasirox, με κύρια διάγνωση β-θαλασσαιμία.
    3. Αξιολόγηση της μεταβολή του σιδήρου στην καρδιά, με την Τ2* MRI τεχνική από τη βασική επίσκεψη σε ασθενείς με SSP-004184AQ ή deferasirox.
    4. Αξιολόγηση της μεταβολή της φερριτίνης πλάσματος από τη βασική επίσκεψη σε ασθενείς με SSP-004184AQ ή deferasirox.
    5. Αξιολόγηση της μεταβολής της LIC από τη βασική επίσκεψη, με την τεχνική R2* MRI σε ασθενείς με υπερσιδήρωση από μεταγγίσεις με SSP-004184AQ ή deferasirox, με κύρια διάγνωση β-θαλασσαιμία.
    6. Αξιολόγηση της μεταβολής του σιδήρου στο πάγκρεας, με την τεχνική R2* MRI σε ασθενείς με υπερσιδήρωση από μεταγγίσεις με SSP-004184AQ ή deferasirox
    E.2.2Secondary objectives of the trial
    Safety

    1. To assess the safety and tolerability of SSP-004184AQ and deferasirox when administered for 48 weeks based upon assessment of LVEF via MRI, TEAEs, clinical laboratory assessments, vital signs, ECGs, Gastrointestinal Symptom Rating Scale, renal function assessments, and the TNSn©.

    2. To describe the exposure/response relationship between various safety parameters and SSP-004184AQ concentrations following administration of SSP-004184AQ.

    3. To explore the potential for early safety markers of kidney function.


    Health Economics Outcomes Research Objectives

    1. To assess Health-Related Quality of Life for subjects treated with SSP-004184AQ and those treated with deferasirox based on a subject self-report of the EQ-5D-3L.
    Ασφάλεια
    1. Η αξιολόγηση της ασφάλειας & ανεκτικότητας των SSP-004184AQ & deferasirox, όταν χορηγούνται επί 48 εβδομάδες, με βάση την αξιολόγηση του κλάσματος εξώθησης της αριστεράς κοιλίας μέσω MRI, των αποδιδόμενων στη θεραπεία ανεπιθύμητων ενεργειών, των αποτελεσμάτων των εργαστηριακών εξετάσεων, των ζωτικών σημείων, του ΗΚΓ, της Κλίμακας Αξιολόγησης Γαστρεντερικών Συμπτωμάτων, της αξιολόγησης της νεφρικής λειτουργίας και της Total Neuropathy Score nurse© (TNSn©).
    2. Nα περιγράψει την σχέση έκθεσης στο φάρμακο/ανταπόκρισης μεταξύ των διαφόρων παραμέτρων ασφάλειας και των συγκεντρώσεων του SSP-004184AQ.
    3. Να διερευνήσει το δυναμικό πρώϊμων δεικτών ασφάλειας της νεφρικής λειτουργίας.

    Φαρμακοοικονομία

    1. Να αξιολογήσει τη σχετιζόμενη με την υγεία Ποιότητα Ζωής (HRQoL) των ασθενών που έλαβαν θεραπεία με SSP-004184AQ και εκείνων που έλαβαν deferasirox, με βάση το συμπληρούμενο από τον ασθενή ερωτηματολόγιο ποιότητας ζωής EQ-5D-3L.
    E.2.3Trial contains a sub-study No
    E.2.3.1Full title, date and version of each sub-study and their related objectives
    No
    E.3Principal inclusion criteria
    1. An understanding, ability, and willingness to fully comply with study procedures and restrictions.

    2. Ability to voluntarily provide written, signed, and dated (personally or via a legally-authorized representative) informed consent as applicable to participate in the study before completing any study-related procedures.

    3. Subjects 18 years of age or older at the time of signing consent.

    4. 1. Female subjects should be one of the following:
    a. Post-menopausal (12 consecutive months of spontaneous amenorrhea)
    b. Surgically sterile or
    c. Females of child child-bearing potential must have a negative serum β-HCG pregnancy test at the Screening Visit (Visit 1) and a negative urine pregnancy test at the Baseline Visit (Visit 3). Females of child-bearing potential must agree to abstain from sexual activity that could result in pregnancy or agree to use acceptable methods of contraception

    5. Subjects with β-thalassemia who have received at least 100mL/kg of packed red blood cells (or >20 transfusion units) and who have iron overload (transfusional hemosiderosis) requiring chronic treatment with an iron chelator.

    6. Serum ferritin >500μg/L at the Screening Visit (Visit 1).

    7. Baseline LIC (last MRI assessment prior to Day 1) ≥2.0mg and <30.0mg iron per g (equivalent dry weight, liver) determined by FerriScan® R2 MRI.

    8. Mean of the previous 3 pre-transfusion hemoglobin concentrations ≥7.5g/dL assessed at the Screening Visit (Visit 1) (1 value from clinical laboratory tests taken at the screening Visit [Visit 1] and the previous 2 historical values available).
    1. Ικανότητα αντίληψης και κατανόησης και προθυμία να συμμορφωθεί πληρως με τις διαδικασίες και τους περιορισμούς της μελέτης.

    2. Ικανότητα να δώσει εθελοντικά την γραπτή, υπογεγραμμένη και χρονολογημένη (προσωπικά ή μέσω εξουσιοδοτημένου αντιπροσώπου) ενημερωμένη συγκατάθεσή του να λάβει μέρος στη μελέτη, πριν συμμετάσχει σε οποιαδήποτε σχετιζόμενη με τη μελέτη διαδικασία.

    3. Ασθενείς ηλικίας 18 ετών ή μεγαλύτερης κατά το χρόνο υπογραφής της ενημερωμένης συγκατάθεσης.

    4. Οι γυναίκες ασθενείς θα πρέπει να είναι ένα από τα ακόλουθα:
    • Mετεμμηνοπαυσιακές (12 συνεχόμενοι μήνες αυτόματης αμηνόρροιας)
    • Χειρουργικώς στείρες ή
    • Οι γυναίκες αναπαραγωγικού δυναμικού πρέπει να έχουν αρνητικό τεστ κυήσεως πλάσματος (β-HCG) κατά την Επίσκεψη Διαλογής (Επίσκεψη 1) και αρνητικό τεστ κυήσεων ούρων κατά τη Βασική Επίσκεψη (Επίσκεψη 3). Οι γυναίκες αναπαραγωγικού δυναμικού πρέπει να συμφωνήσουν να επέχουν από σεξουαλική δραστηριότητα η οποία θα μπορούσε να οδηγήσεις σε εγκυμοσύνη ή να συμφωνήσουν να χρησιμοποιούν αποδεκτές μεθόδους αντισύλληψης.

    5. Ασθενείς με β-θαλασσαιμία οι οποίοι έχουν λάβει τουλάχιστον 100 mL/kg συμπυκνωμένων ερυθροκυττάρων (ή > 20 μονάδες αίματος μετάγγιση) και οι οποίοι έχουν υπερφόρτωση σιδήρου (αιμοσιδήρωση εκ μεταγγίσεως) και απαιτούν χρόνια θεραπεία με ένα χηλικό παράγοντα αποσιδήρωσης.

    6. Φερριτίνη ορού > 500 μg/L κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    7. Συγκέντρωση σιδήρου ήπατος (LIC) κατά τη Βασική Επίσκεψη (τελευταία αξιολόγηση με MRI πριν από την Ημέρα 1) ≥ 2.0 mg και < 30.0 mg σιδήρου ανά g (ισοδύναμου ξηρού βάρους ήπατος), προσδιορισμένη με μέθοδο FerriScan R2 MRI.

    8. Μέση τιμή των 3 προηγούμενων προ-της-μετάγγισης συγκεντρώσεων αιμοσφαιρίνης ≥ 7.5 g/dL, αξιολογημένη κατά την Επίσκεψη Διαλογής (Screening) (Επίσκεψη 1) (1 τιμή από τις εργαστηριακές εξετάσεις κατά την Επίσκεψη Διαλογής [Επίσκεψη 1] και οι διαθέσιμες 2 προηγούμενες ιστορικές τιμές)
    E.4Principal exclusion criteria
    1. Severe iron overload including: (a) cardiac T2* MRI <10.0ms; or (b) LIC by FerriScan® R2 MRI ≥30.0mg/g liver (dw) as assessed at the Screening Visit (Visit 1).

    2. Iron overload from causes other than transfusional siderosis.

    3. Subjects with thalassemia intermedia

    4. Unable to undergo MRI assessment.

    5. Cardiac LVEF of <50% at baseline testing by MRI.

    6. Subjects with documented liver failure (presence of portal hypertension, hepatic edema, ascites, cirrhosis), Child-Pugh C hepatic impairment, or biliary disorder .

    7. Platelet count <100 x 109/L at the Screening Visit (Visit 1).

    8. Absolute neutrophils counts of <1500mm3 at the Screening Visit (Visit 1).

    9. Evidence of renal insufficiency eg, creatinine clearance <60mL/min or serum creatinine >1.5 x ULN at the Screening Visit (Visit 1).

    10. Clinically significant laboratory assessments at the Screening Visit (Visit 1).

    11. Significant proteinuria: urinary protein/creatinine ratio >1.0 in a non-first void urine sample at the Screening Visit (Visit 1).

    12. Current or recurrent disease that could affect the action, absorption, or disposition of the investigational product, or clinical or laboratory assessments.

    13. Current or relevant history of physical or psychiatric illness, any medical disorder that may require treatment or make the subject unlikely to fully complete the study, or any condition, including pregnancy, that presents undue risk from the investigational product or procedures.

    14. Current use of any medication contraindicated in the deferasirox prescribing information/SmPC. See prescribing information/SmPC for a list of prohibited and restricted medications.

    15. Known or suspected intolerance or hypersensitivity to SSP-004184AQ, deferasirox,closely-related compounds, or any of the stated ingredients in either medication.

    16. Known history of alcohol or other substance abuse within the last year.

    17. Within 30 days prior to the Baseline Visit (Visit 3):
    - Have used an investigational product
    - Have been enrolled in a clinical study (including vaccine studies) that, in the investigator’s opinion, may impact this Shire-sponsored study

    18. History of malignancy within the past 5 years, with the exception of basal cell or squamous cell skin carcinoma or cervical carcinoma in situ or completely resected colon carcinoma in situ.

    19. Insufficient venous access that precludes prescribed blood draws for safety laboratory assessments.

    20. Pregnant or lactating females.
    1. Σοβαρή υπερσιδήρωση συμπεριλαμβάνουσα: (a) καρδιακή T2* MRI < 10.0 ms ή (b) ηπατική συγκέντρωση σιδήρου (LIC) μετρηθείσα με FerriScan R2 MRI ≥ 30.0 mg/g ήπατος (ξηρού βάρους) αξιολογημένη κατά την Επίσκεψη Διαλογής (Επίσκεψη 1).

    2. Υπερσιδήρωση από αιτίες άλλες εκτός από σιδήρωση εκ μεταγγίσεων

    3. Ασθενείς με ενδιάμεση θαλασσαιμία

    4. Ασθενείς ανίκανοι να υποβληθούν σε ΜRI

    5. Κλάσμα εξώθησης αριστεράς κοιλίας <50% κατά τη Βασική Επίσκεψη μετρούμενo με MRI.

    6. Ασθενείς με τεκμηριωμένη ηπατική ανεπάρκεια (παρουσία πυλαίας υπέρτασης, ηπατικού οιδήματος, ασκίτη, κίρρωσης), ηπατική δυσλειτουργία βαθμού C κατά Child-Pugh ή παθήσεις των χοληφόρων .

    7. Αριθμός αιμοπεταλίων <100 x 109/L κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    8. Απόλυτος αριθμός ουδετεροφίλων <1.500/mm3 κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    9. Ενδείξεις νεφρικής ανεπάρκειας π.χ. κάθαρση κρεατινίνης < 60 mL/min ή κρεατινίμη ορού > 1.5 x AΦΤ κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    10. Κλινικά σημαντικές εργαστηριακές αξιολογήσεις κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    11. Σημαντική πρωτεϊνουρία: πρωτεϊνη ούρων / κρεατινίνη > 1.0 σε ένα δείγμα ούρων όχι της πρώτης πρωϊνής κένωσης, κατά την Επίσκεψη Διαλογής (Επίσκεψη 1)

    12. Τρέχουσα ή υποτροπιάζουσα νόσος η οποία μπορεί να επηρεάσει τη δράση, την απορρόφηση ή την κατανομή του ερευνητικού φαρμάκου ή τις κλινικές ή εργαστηριακές αξιολογήσεις.

    13. Τρέχον ή σχετικό ιστορικό οργανικής ή ψυχιατρικής νόσου, κάθε διαταραχή η οποία απαιτεί θεραπεία ή καθιστά τον ασθενή πιθανώς ανίκανο να ολοκληρώσει τη συμμετοχή του στη μελέτη ή κάθε ιατρική κατάσταση, συμπεριλαμβανόμενης της κύησης, η οποία παρουσιάζει αδικαιολόγητο κίνδυνο από το ερευνητικό φάρμακο ή τις διαδικασίες της μελέτης.

    14. Τρέχουσα χρήση οποιουδήποτε φαρμάκου αντενδείκνυται στην Περίληψη Χαρακτηριστικών Προϊόντος (ΠΧΠ) του deferasirox

    15. Γνωστή ή πιθανή δυσανεξία ή υπερευαισθησία στο SSP-004184AQ, το deferasirox, σχετιζόμενης δομής προϊόντα, ή σε οποιοδήποτε από τα συστατικά αμφορτέρων των φαρμάκων.

    16. Γνωστό ιστορικό αλκοολισμού ή κατάχρησης ουσιών εντός του τελευταίου έτους.

    17. Ο ασθενής, εντός των τελευταίων 30 ημερών πριν από τη Βασική Επίσκεψη (επίσκεψη 3):
    - έχει χρησιμοποιήσει οποιοδήποτε ερευνητικό προϊόν
    - έχει ενταχθεί σε κάποια κλινική μελέτη (συμπεριλαμβανόμενων μελετών για εμβόλια) η οποία, κατά τη γνώμη του ερευνητή, δυνατόν να επηρεάσει την χορηγούμενη από τη Shire μελέτη

    18. Ιστορικό κακοήθειας εντός των προηγουμένων 5 ετών, με εξαίρεση του βασικοκυτταρικού καρκινώματος του δέρματος ή δερματικού καρκινώματος εκ πλακωδών επιθηλιακών κυττάρων ή in situ καρκινώματος τραχήλου της μήτρας ή πλήρως εξαιρεθέντος in situ καρκινώματος του παχέος εντέρου.

    19. Ανεπαρκής πρόσβαση σε φλέβα, η οποία αποκλείει τις προγραμματισμένες αιμοληψίες για τις εργαστηριακές εξετάσεις ασφάλειας.

    20. Εγκυες γυναίκες και θηλάζουσες μητέρες
    E.5 End points
    E.5.1Primary end point(s)
    • Change from baseline in Liver Iron Concentration (LIC) as assessed by FerriScan® R2 at Weeks 12, 24, and 48.
    • Rate of response defined according to the criteria listed in the protocol assessed by FerriScan® R2 at Weeks 12, 24, and 48.
    • Change from baseline in Cardiac Iron Concentration (CIC) as assessed by T2* MRI at Weeks 12, 24, and 48
    • Change from baseline in serum ferritin at Weeks 12, 24, and 48.
    • Change from baseline in LIC as assessed by R2* MRI at Weeks 12, 24, and 48.
    • Change from baseline in Pancreatic Iron Concentration (PIC) as assessed by R2* MRI at Weeks 12, 24, and 48.
    • Treatment-emergent AEs graded and recorded according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.0
    • Vital signs measurements at Week 48
    • Clinical laboratory tests (chemistry, hematology, and urinalysis) at Weeks, 2, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, and 48.
    • 12-lead electrocardiogram at Weeks 12, 24, and 48
    • Left ventricular ejection fraction via MRI at Weeks 12, 24, and 48
    • Renal function assessments (serum creatinine and estimated glomerular filtration rate) at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, and 48
    • Gastrointestinal Symptom Rating Scale at Weeks 2, 4, 8, 12, 24, 36, and 48.
    • Total Neuropathy Score nurse© at weeks 4, 12, 24, 36, and 48.
    • Change from baseline in Health-Related Quality of Life assessment (based on subject self report of the EQ-5D-3L) at Weeks 12, 24, and 48 or at discontinuation.
    • Μεταβολή από τη βασική της τιμή της ηπατικής συγκέντρωσης σιδήρου (LIC), αξιολογηθείσα με FerriScan R2 MRI τις Εβδομάδες 12, 24 και 48.
    • Ποσοστό ανταπόκρισης (οριζόμενο σύμφωνα με τα κριτήρια που απαριθμούνται στη συνέχεια), αξιολογημένο με με FerriScan R2 MRI τις Εβδομάδες 12, 24 και 48.
    • Μεταβολή από τη βασική της τιμή της καρδιακής συγκεντρώσης σιδήρου (CIC), αξιολογηθείσα με T2* MRI τις Εβδομάδες 12, 24 και 48.
    • Μεταβολή από τη βασική της τιμή της φερριτίνης πλάσματος, τις Εβδομάδες 12, 24 και 48.
    • Μεταβολή από τη βασική της τιμή της ηπατικής συγκέντρωσης σιδήρου (LIC), αξιολογηθείσα με R2* MRI τις Εβδομάδες 12, 24 και 48.
    • Μεταβολή από τη βασική της τιμή της παγκρεατικής συγκέντρωσης σιδήρου, αξιολογηθείσα με R2* MRI τις Εβδομάδες 12, 24 και 48.
    • Αποδιδόμενες στη θεραπεία ανεπιθύμητες ενέργειες, βαθμονομημένες και ταξινομημένες σύμφωνα με τα Common Terminology Criteria for Adverse Events του National Cancer Institute (NCI) των ΗΠΑ, έκδοση 4.0 (CTCAE)
    • Μετρήσεις ζωτικών σημείων την Εβδομάδα 48
    • Εργαστηριακές εξετάσεις (βιοχημικές, αιματολογικές και ούρων) τις Εβδομάδες 2, 4, 8, 12, 16, 20, 24, 28, 32, 26, 40, 44 και 48
    • ΗΚΓ 12 απαγωγών τις Εβδομάδες 12, 24 και 48
    • Κλάσμα εξώθησης αριστεράς κοιλίας, μέσω MRI, τις εβδομάδες 12, 24 και 48.
    • Aξιολόγηση νεφρικής λειτουργίας (κρεατινίνη ορού & εκτιμώμενος ρυθμός σπειραματικής διήθησης) τις Εβδομάδες 2, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44και 48
    • Kλίμακα Αξιολόγησης Γαστρεντερικών Συμπτωμάτων τις Εβδομάδες 2, 4, 8, 12, 24, 36 και 48
    • TNSn© στην Επίσκεψη Διαλογής (screening) και στις Εβδομάδες 4, 12, 24, 36 και 48
    • Η μεταβολή από τη βασική τιμή της βαθμολογίας του Σχετιζόμενου με την Υγεία Ερωτηματολογίου Ποιότητας Ζωής (αυτοσυμπληρούμενο από τον ασθενή ερωτηματολόγιο EQ-5D-3L) τις Εβδομάδες 12, 24 και 48 ή κατά τη διακοπή της θεραπείας.
    E.5.1.1Timepoint(s) of evaluation of this end point
    Timepoints included above
    Tα χρονικά σημεία εκτίμησης των κύριων τελικών σημείων περιλαμβάνονται ανωτέρω
    E.5.2Secondary end point(s)
    Not Applicable
    Δεν εφαρμοζεται
    E.5.2.1Timepoint(s) of evaluation of this end point
    Not Applicable
    Δεν εφαρμοζεται
    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 Yes
    E.6.10Pharmacogenetic Yes
    E.6.11Pharmacogenomic Yes
    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) 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 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) No
    E.8.2.2Placebo No
    E.8.2.3Other No
    E.8.2.4Number of treatment arms in the trial2
    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 concerned2
    E.8.5The trial involves multiple Member States Yes
    E.8.5.1Number of sites anticipated in the EEA16
    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
    Australia
    Belgium
    Canada
    Egypt
    France
    Germany
    Greece
    Israel
    Italy
    Lebanon
    Saudi Arabia
    Thailand
    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 years1
    E.8.9.1In the Member State concerned months6
    E.8.9.1In the Member State concerned days
    E.8.9.2In all countries concerned by the trial years1
    E.8.9.2In all countries concerned by the trial months6
    F. Population of Trial Subjects
    F.1 Age Range
    F.1.1Trial has subjects under 18 No
    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) No
    F.1.1.6Adolescents (12-17 years) No
    F.1.2Adults (18-64 years) Yes
    F.1.2.1Number of subjects for this age range: 49
    F.1.3Elderly (>=65 years) Yes
    F.1.3.1Number of subjects for this age range: 1
    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 No
    F.3.3.7Others No
    F.4 Planned number of subjects to be included
    F.4.1In the member state4
    F.4.2 For a multinational trial
    F.4.2.1In the EEA 27
    F.4.2.2In the whole clinical trial 50
    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)
    Subjects participating in this study may be offered the opportunity to participate in a safety extension study where subjects will receive treatment with SSP-004184AQ. Subjects who are not eligible or choose not to participate will be treated according to standard of care as recommended by the subject's physician.
    Στους ασθενείς που θα συμμευάσχουν στη μελέτη δυνατόν να προσφερθεί η ευκαιρία να συμμετάσχουν σε μία μελέτη επέκτασης για έλεγχο της ασφάλειας στην οποία οι ασθενείς θα λαμβάνουν θεραπεία με το SSP-004184AQ. Οι ασθενείς που δεν είναι κατάλληλοι για ένταξη στη μελέτη επέκτασης ή επιλέγουν να μην συμμετάσχουν θα αντιμετωπιστούν σύμφωνα με την πρότυπη ιατρική φροντίδα, σύμφωνα με τη σύσταση του θεράποντος ιατρού τους.
    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 Decision2014-01-27
    N.Ethics Committee Opinion of the trial applicationFavourable
    N.Ethics Committee Opinion: Reason(s) for unfavourable opinion
    N.Date of Ethics Committee Opinion2014-01-14
    P. End of Trial
    P.End of Trial StatusPrematurely Ended
    P.Date of the global end of the trial2014-07-15
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