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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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23 November 2020 |
Main ID: |
EUCTR2017-004279-30-NL |
Date of registration:
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16/05/2018 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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A clinical study to assess the long-term safety and efficacy of idebenone treatment in patients with Duchenne Muscular Dystrophy (DMD) who completed the SIDEROS study.
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Scientific title:
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A Phase III Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of Idebenone in Patients with Duchenne Muscular Dystrophy (DMD) who completed the SIDEROS study - SIDEROS-E |
Date of first enrolment:
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23/01/2020 |
Target sample size:
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266 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2017-004279-30 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no Randomised: no Open: yes Single blind: no Double blind: no Parallel group: no Cross over: no Other: no If controlled, specify comparator, Other Medicinial Product: no Placebo: no Other: no
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Phase:
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Human pharmacology (Phase I): no
Therapeutic exploratory (Phase II): no
Therapeutic confirmatory - (Phase III): yes
Therapeutic use (Phase IV): no
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Countries of recruitment
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Austria
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Belgium
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France
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Germany
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Israel
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Italy
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Netherlands
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Spain
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Sweden
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Switzerland
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United Kingdom
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United States
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Contacts
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Name:
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Anna Carratu
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Address:
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Hohenrainstrasse 24
4133
Pratteln
Switzerland |
Telephone:
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+4161906 8917 |
Email:
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anna.carratu@santhera.com |
Affiliation:
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Santhera Pharmaceuticals (Switzerland) Limited |
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Name:
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Anna Carratu
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Address:
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Hohenrainstrasse 24
4133
Pratteln
Switzerland |
Telephone:
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+4161906 8917 |
Email:
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anna.carratu@santhera.com |
Affiliation:
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Santhera Pharmaceuticals (Switzerland) Limited |
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Key inclusion & exclusion criteria
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Inclusion criteria: Completion of the SIDEROS study at Visit 8/ Week 78.
Signed and dated Informed Consent Form.
Are the trial subjects under 18? yes Number of subjects for this age range: 266 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 40 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria: Patients who discontinued SIDEROS study prematurely (i.e. did not attend all visits from V1 to V8).
Safety, tolerability or other issues arising during the course of the SIDEROS study which in the opinion of the Investigator may put the patient at significant risk or may interfere significantly with the patient’s participation in the SIDEROS-E study.
Use of any investigational drug other than the study medication.
Enrolment in SIDEROS-E of siblings of randomized SIDEROS patients is allowed if they meet all the inclusion and none of the exclusion criteria above.
Age minimum:
Age maximum:
Gender:
Female: no Male: yes
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Health Condition(s) or Problem(s) studied
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Duchenne Muscular Dystrophy (DMD) MedDRA version: 20.0
Level: PT
Classification code 10013801
Term: Duchenne muscular dystrophy
System Organ Class: 10010331 - Congenital, familial and genetic disorders
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Therapeutic area: Diseases [C] - Musculoskeletal Diseases [C05]
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Intervention(s)
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Trade Name: Raxone Product Name: Idebenone Pharmaceutical Form: Film-coated tablet INN or Proposed INN: IDEBENONE CAS Number: 58186-27-9 Other descriptive name: IDEBENONE Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 150-
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Primary Outcome(s)
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Timepoint(s) of evaluation of this end point: Electrocardiogram: baseline Adverse events, safety laboratory parameters, vital signs: 26 weeks , 52 weeks, 78 weeks, 82 weeks
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Primary end point(s): Primary: Standard safety assessments, including number of premature discontinuations of study treatment due to adverse events, incidence and severity of adverse events, actual values and changes from baseline in safety laboratory parameters, vital signs and electrocardiogram (ECG).
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Main Objective: To assess the long-term safety of idebenone in DMD patients who completed the SIDEROS study.
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Secondary Objective: To describe the long-term evolution of respiratory function in idebenone-treated DMD patients who completed the SIDEROS study, classified by background factors including, but not limited to age, DMD history (e.g. time of loss of ambulation, mutation type), type of steroid regimen and study treatment assignment in the SIDEROS study.
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Secondary Outcome(s)
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Secondary end point(s): Secondary:
Change from Baseline in Forced Vital Capacity (FVC) as percent of predicted (FVC%p), Peak Expiratory Flow (PEF) as percent of predicted (PEF%p) and Forced Expiratory Volume in 1 second (FEV1) as percent of predicted (FEV1%p).
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Timepoint(s) of evaluation of this end point: Forced Vital Capacity (FVC), Peak Expiratory Flow (PEF)Forced Expiratory Volume in 1 second (FEV1) : baseline, 26 weeks , 52 weeks, 78 weeks
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Secondary ID(s)
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103801
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2017-004279-30-BE
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SNT-III-012-E
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Source(s) of Monetary Support
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Santhera Pharmaceuticals (Switzerland) Limited
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Ethics review
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Status: Approved
Approval date: 23/01/2020
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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