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| Found 69 studies with search of: | "Muscular Dystrophy" |
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Recruiting |
Evaluation of Limb-Girdle Muscular Dystrophy
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| 2 | Active, not recruiting |
Phase 2b Study of PTC124 in Duchenne/Becker Muscular Dystrophy (DMD/BMD)
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| 3 | Completed |
Gentamicin Treatment of Muscular Dystrophy
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| 4 | Active, not recruiting |
Phase 2b Extension Study of Ataluren (PTC124) in Duchenne/Becker Muscular Dystrophy (DMD/BMD)
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| 5 | Recruiting |
Study of Ataluren (PTC124®) in Nonambulatory Patients With Nonsense-Mutation-Mediated Duchenne/Becker Muscular Dystrophy (nmDMD/BMD)
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| 6 | Active, not recruiting |
The Efficacy of Using Far Infrared Radiation to Manage Muscular Dystrophies
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| 7 | Recruiting |
Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy
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| 8 | Recruiting |
Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry
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| 9 | Recruiting |
Test-Retest Reliability of Pulmonary Function Tests in Patients With Duchenne's Muscular Dystrophy
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| 10 | Completed |
High-Dose Prednisone in Duchenne Muscular Dystrophy
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| 11 | Recruiting |
Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)
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| 12 | Recruiting |
A Clinical Evaluation of FKRP Muscular Dystrophy
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| 13 | Completed |
Safety and Efficacy Study of PTC124 in Duchenne Muscular Dystrophy
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| 14 | Recruiting |
Ramipril Versus Carvedilol in Duchenne and Becker Patients
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| 15 | Active, not recruiting |
Safety Study of Mini-Dystrophin Gene to Treat Duchenne Muscular Dystrophy
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| 16 | Active, not recruiting |
Arrhythmias in Myotonic Muscular Dystrophy
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| 17 | Recruiting |
The Preventive Efficacy of Carvedilol on Cardiac Dysfunction in Duchenne Muscular Dystrophy
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| 18 | Active, not recruiting |
Phase 2a Extension Study of Ataluren (PTC124) in Duchenne Muscular Dystrophy (DMD)
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| 19 | Active, not recruiting |
Safety and Efficacy Study of Antisense Oligonucleotides in Duchenne Muscular Dystrophy
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| 20 | Completed |
Efficacy and Tolerability of Idebenone in Boys With Cardiac Dysfunction Associated With Duchenne Muscular Dystrophy
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