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PubPharm (1.626)
1
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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2
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)
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| 2024
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3
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
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| 2024
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4
Upper Extremity Muscle Strength, Balance and Functional Skills in DMD : The Association Between Upper Extremity Muscle Strength, Balance and Functional Skills in Children With Duchenne Muscular Dystrophy
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| 2024
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5
Motor Outcomes to Validate Evaluations in FSHD (MOVE FSHD) : Motor Outcomes to Validate Evaluations in FSHD (MOVE FSHD)
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| 2024
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6
Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project [RIMUDI] : Rehabilitation in Muscular Dystrophies From the Hospital Facility to the Home: Pilot Project
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| 2024
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7
Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy : Pilot Study to Assess Biomarkers of Changes in Barrier Function of Skeletal Muscle in Patients With a Fragile Sarcolemmal Muscular Dystrophy
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| 2024
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8
Genetic and Physical Study of Childhood Nerve and Muscle Disorders : Clinical and Molecular Manifestations of Neuromuscular and Neurogenetic Disorders of Childhood
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| 2024
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9
At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions : A Multi-Site Tissue Repository Providing Annotated Biospecimens for Approved Investigator-Directed Biomedical Research Initiatives
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| 2024
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10
Study of Inherited Neurological Disorders : Clinical and Molecular Manifestations of Inherited Neurological Disorders
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Thema: 610
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Study Type: Interventional
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Muscular Dystrophies
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Recruitment Status: Not yet recruiting
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Phase: Phase 3
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Muscular Dystrophy, Duchenne
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Recruitment Status: Completed
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Study Type: Observational
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Phase: Phase 2
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Recruitment Status: Recruiting
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Recruitment Status: Authorised-recruitment may ...
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Phase: Phase 1
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Medical Condition: Duchenne Muscular Dystrophy
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Medical Condition: Duchenne Muscular Dystrophy ...
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Medical Condition: Duchenne muscular dystrophy
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Muscular Dystrophy, Facioscapulohumeral
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Muscular Dystrophies, Limb-Girdle
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Recruitment Status: Active, not recruiting
51
Recruitment Status: Terminated
50
Recruitment Status: Complete: follow-up complete
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