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Myotonic Dystrophy

Clinical trial condition

Myotonic Dystrophy

Explore clinical trials studying Myotonic Dystrophy. Study availability and eligibility vary by location and protocol.

107 public trials 35 recruiting studies

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Myotonic Dystrophy trial results

Recruiting

Remote Assessments and Genetic Determinants of Congenital and Childhood Myotonic Dystrophy

NCT07630389

Conditions: Childhood DM1, Congenital DM1, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +13 more
Locations: University of Rochester Rochester, New York, United States

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Recruiting

Efficacy, Safety, and Tolerability of Zeleciment Rostudirsen (DYNE-251) Administered Intravenously Every 4 Weeks in Ambulatory Participants With Duchenne Muscular Dystrophy (FORZETTO)

NCT07608432

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DMD, Duchenne Muscular Dystrophy (DMD), +21 more
Locations: Rare Disease Research, LLC Hillsborough, North Carolina, United States

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Recruiting

Assessment of a Portable Digital Device for Quantified Analysis of Markerless Walking in Volunteers With Neuromuscular Diseases or Asymptomatic Volunteers

NCT07321977

Conditions: Central Nervous System Diseases, Charcot-Marie-Tooth, Charcot-Marie-Tooth Disease, +25 more
Locations: Centre d'Exploration et d'Évaluation Neuromusculaire Paris, France

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Recruiting

A Clinical Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1

NCT06667453

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: University of Calgary Calgary, Alberta, Canada

Ottawa Hospital Research Institute (OHRI) Ottawa, Ontario, Canada

CIUSSS du Saguenay-Lac-Saint-Jean Chicoutimi, Quebec, Canada

Montreal Neurological Institute Montreal, Quebec, Canada

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Recruiting

Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

NCT06147414

Conditions: Abnormalities, Multiple, Anemia, Anemia, Hemolytic, +78 more
Locations: Hôpital Cochin, Maternité Port-Royal, service de Gynécologie obstétrique Paris, France

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Recruiting

Investigating Exercise in Myotonic Dystrophy Type 2 (DM2)

NCT06716931

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
Locations: Neuromuscular Diagnostic Center. Massachusetts General Hospital Boston, Massachusetts, United States

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Recruiting

Remote Assessments and Genetic Determinants of Myotonic Dystrophy

NCT07505342

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +11 more
Locations: University of Rochester Rochester, New York, United States

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Recruiting

An Open-Label Extension Study of PGN-EDODM1 in People With Myotonic Dystrophy Type 1 (FREEDOM-OLE)

NCT07220603

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: University of Calgary Calgary, Alberta, Canada

Ottawa Hospital Research Institute Ottawa, Ontario, Canada

CIUSSS du Saguenay-Lac-Saint-Jean Saguenay, Canada

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Recruiting

Evaluation of the Role of miR-1 in the Pathogenesis and as a Biomarker in Muscular Dystrophies and Congenital Myopathies

NCT07415837

Conditions: Congenital Myopathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne / Becker Muscular Dystrophy, +16 more
Locations: CHU de Clermont-Ferrand Clermont-Ferrand, France

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Recruiting

Study of ATX-01 in Participants With DM1

NCT06300307

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: UCLA Los Angeles, California, United States

University of Florida Gainesville, Florida, United States

University of Iowa Health Care - Department of Neurology Iowa City, Iowa, United States

University of Kansas Medical Center, Department of Neurology Fairway, Kansas, United States

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