Example: Heart Attack

Clinical Trials on Centronuclear Myopathy

Total 6 results

NCT04743557

Not yet recruiting

Early Phase Human Drug Trial to Investigate DYN101 in Participants 2 to 17 Years With Centronuclear Myopathies

Conditions: Centronuclear Myopathy
NCT04033159

Recruiting

Early Phase Human Drug Trial to Investigate Dynamin 101 (DYN101) in Patients ≥ 16 Years With Centronuclear Myopathies

Conditions: Centronuclear Myopathy
NCT03351270

Recruiting

Prospective Natural History Study of Patients With Myotubular Myopathy and Other CentroNuclear Myopathies

Conditions: Centronuclear Myopathy
NCT00272883

Recruiting

Molecular and Genetic Studies of Congenital Myopathies

Conditions: Central Core Disease, Centronuclear Myopathy, Congenital Fiber Type Disproportion, Multiminicore Disease, Myotubular Myopathy, Nemaline Myopathy, Rigid Spine Muscular Dystrophy, Undefined Congenital Myopathy
NCT04064307

Recruiting

Myotubular and Centronuclear Myopathy Patient Registry

Conditions: Myotubular Myopathy, Myotubular Myopathy 1, Myotubular (Centronuclear) Myopathy, Centronuclear Myopathy, Centronuclear Myopathy, X-Linked, X-linked Myotubular Myopathy
NCT01403402

Unknown status

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Conditions: Congenital Muscular Dystrophy (Including Unspecified/Undiagnosed), Dystroglycanopathy, Congenital Fiber Type Disproportion, Rigid Spine Muscular Dystrophy, Congenital Myopathy (Including Unspecified/Undiagnosed), Collagen VI CMD (Ullrich CMD, Intermediate, Bethlem Myopathy), Laminin Alpha 2 Related Congenital Muscular Dystrophy, LAMA2-CMD/Merosin Deficient/MDC1A, Walker-Warburg Syndrome, Muscle-Eye-Brain Disease, Fukuyama/Fukutin Related Muscular Dystrophy, Integrin Alpha 7 Deficiency, Integrin Alpha 9 Deficiency, LMNA-CMD/Lamin A/C/Laminopathy, SEPN1-Related Myopathy, Bethlem Myopathy, Actin Aggregation Myopathy, Cap Disease, Central Core Disease, Centronuclear Myopathy, Core Rod Myopathy, Hyaline Body Myopathy, Multiminicore Myopathy, Myotubular Myopathy, Nemaline Myopathy, Tubular Aggregate Myopathy, Zebra Body Myopathy, Reducing Body Myopathy, Spheroid Body Myopathy, LGMD1B (LMNA), LGMD1E (DES), LGMD2G (TCAP), LGMD2H (TRIM32), LGMD2I (FKRP), LGMD2J (TTN), LGMD2K (POMT1), LGMD2M (FKTN), LGMD2N (POMT2), LGMD2O (POMGnT1), LGMD2P (DAG1), LGMD2Q (PLEC1), LGMD2R (DES), LGMD2S (TRAPPC11), LGMD2T (GMPPB), LGMD2U (ISPD), LGMD2V (GAA), Ullrich Congenital Muscular Dystrophy, Titinopathy, Choline Kinase B Receptor, Emery-Dreifuss Muscular Dystrophy, RYR1 Related Myopathy, SYNE1/Nesprin Related Muscular Dystrophy, Telethonin Related Muscular Dystrophy (TCAP/Titin-Cap), Congenital Myasthenic Syndrome, Escobar Syndrome, Myofibrillar Myopathy, Malignant Hyperthermia, Alpha-Dystroglycan Related Muscular Dystrophy (DAG1, DPM1, DPM2, DPM3, FKRP, FKTN), Alpha-Dystroglycan Related Muscular Dystrophy (GAA, ISPD, LARGE, POMT1, POMT2, POMGnT1), Alpha-Dystroglycan Related Muscular Dystrophy (Unspecified/Undiagnosed/Other)