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topic_facet:"Study Type: Interventional"
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/vufind/Search/Results?lookfor=%22muscular+dystrophy%22&type=Subject&filter%5B%5D=topic_facet%3A%22Study+Type%3A+Interventional%22
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PubPharm (1.341)
1
A Study Of PGN-EDO51 In Participants With Duchenne Muscular Dystrophy Amenable To Exon 51-Skipping Treatment : A Phase 2, Open-Label, Multiple Ascending Dose Study of PGN-EDO51 With a Long-Term Extension in Participants With Duchenne Muscular Dystrophy Amenable to Exon 51-Skipping Treatment (CONNECT1-EDO51)
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| 2024
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2
A Study to Evaluate the Safety and Tolerability of GEN6050X in Duchenne Muscular Dystrophy. : A Single-arm, Open-label, Single-center Study to Evaluate the Safety and Tolerability of Intravenous GEN6050X Gene Therapy in Ambulatory Boys With Duchenne Muscular Dystrophy (DMD).
enthalten in:
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| 2024
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3
Study to Evaluate the Efficacy and Safety of BBP-418 (Ribitol) in Patients With Limb Girdle Muscular Dystrophy 2I (LGMD2I) : A Phase 3 Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of BBP-418 (Ribitol) in Patients With Limb Girdle Muscular Dystrophy 2I (LGMD2I)
enthalten in:
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| 2024
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4
Study of AOC 1044 in Healthy Adult Volunteers and Participants With Duchenne Muscular Dystrophy (DMD) Mutations Amenable to Exon 44 Skipping : A Phase 1/2, Randomized, Placebo-controlled, Double-blind, Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamic Effects of Single and Multiple Ascending Doses of AOC 1044 Administered Intravenously to Healthy Adult Volunteers and Participants With DMD Mutations Amenable to Exon 44 Skipping
enthalten in:
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| 2024
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5
Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study : Gait Analysis Parameter, Stair Climbing and Upper Limb Evaluation in Patients With Muscular Pathology and in Control Subjects: The ActiLiège Next Study
enthalten in:
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| 2024
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6
Study of Ataluren in Previously Treated Participants With Nonsense Mutation Dystrophinopathy (nmDBMD) : An Open-Label, Safety Study for Ataluren (PTC124) Patients With Nonsense Mutation Dystrophinopathy
enthalten in:
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| 2024
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7
A Study to Evaluate RO7204239 in Participants With Facioscapulohumeral Muscular Dystrophy : A Phase II, Multicenter, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate the Pharmacodynamics, Safety, Tolerability, Pharmacokinetics, and Efficacy of RO7204239 in Participants With Facioscapulohumeral Muscular Dystrophy
enthalten in:
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| 2024
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8
Halt cardiomyOPathy progrEssion in Duchenne (HOPE-OLE) : Open-Label Extension of the Halt Cardiomyopathy Progression in Duchenne (HOPE-Duchenne) Trial (CAP-1002-DMD-03)
enthalten in:
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| 2024
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9
COMMAND Early Feasibility Study: Implantable BCI to Control a Digital Device for People With Paralysis : Motor NeuroProsthesis to Restore Motor Control for the COMMAND of Digital Devices: An Early Feasibility Study (EFS) of Safety in Subjects With Severe Quadriparesis
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| 2024
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10
A Long-term Follow-up Study of Participants Who Received Delandistrogene Moxeparvovec (SRP-9001) in a Previous Clinical Study : A Phase 3, Multinational, Long-term Follow-up Study to Evaluate Safety and Efficacy in Subjects Who Have Previously Received SRP-9001 in a Clinical Study
enthalten in:
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| 2024
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Thema: Study Type: Interventional
Medienart
1.341
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Zeitschriftentitel
930
WHO International Clinical Trials Registry Plat...
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ClinicalTrials.gov
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1.341
610
Study Type: Interventional
524
Recruitment Status: Not yet recruiting
428
Phase: Phase 3
404
Muscular Dystrophies
291
Muscular Dystrophy, Duchenne
265
Phase: Phase 2
243
Recruitment Status: Completed
194
Recruitment Status: Authorised-recruitment may ...
158
Phase: Phase 1
154
Recruitment Status: Recruiting
105
Medical Condition: Duchenne Muscular Dystrophy
88
Medical Condition: Duchenne Muscular Dystrophy ...
45
Recruitment Status: Terminated
38
Medical Condition: Duchenne muscular dystrophy
38
Phase: Phase 1, Phase 2
37
Muscular Dystrophy, Facioscapulohumeral
36
Medical Condition: Duchenne Muscular Dystrophy ...
34
Recruitment Status: Active, not recruiting
32
Recruitment Status: Complete: follow-up complete
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