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NCT07486934
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +18 more
- Locations
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- UCSD - Altman Clinical and Translational Research Institute La Jolla, California, United States
- Rare Disease Research, LLC Atlanta, Georgia, United States
- IU Health Neuroscience Center Indianapolis, Indiana, United States
- Roy Blunt NextGen Precision Health Institute Columbia, Missouri, United States
Recruiting
Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1) Extension
NCT07700225
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +20 more
- Locations
-
- Virginia Commonwealth University Richmond, Virginia, United States
NCT06708468
- Conditions
- Charcot Marie Tooth Disease (CMT), Charcot-Marie-Tooth Disease, Congenital Abnormalities, +20 more
- Locations
-
- Haukeland University Hospital Bergen, Norway
- Helse Møre and Romsdal HF (Molde Hospital) Molde, Norway
- Namsos Hospital Namsos, Norway
- Oslo University Hospital Oslo, Norway
NCT05224778
- Conditions
- CDM, Congenital Myotonic Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
- Locations
-
- University of California, Los Angeles Los Angeles, California, United States
- University of Kansas Medical Center Fairway, Kansas, United States
- University of Rochester Medical Center Rochester, New York, United States
- Virginia Commonwealth University Richmond, Virginia, United States
NCT03981575
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +11 more
- Locations
-
- University of California, San Diego La Jolla, California, United States
- University of California, Los Angeles Los Angeles, California, United States
- University of Colorado - Denver Denver, Colorado, United States
- University of Florida Gainesville, Florida, United States
NCT06185764
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +15 more
- Locations
-
- Stanford Neuromuscular Research San Carlos, California, United States
- University of Florida Clinical Research Center Gainesville, Florida, United States
- University of Kansas Medical Center Fairway, Kansas, United States
- Boston Children's Hospital Boston, Massachusetts, United States
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
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
- Locations
-
- University of Florida, 2004 Mowry Road - Site Number: 8400005 Gainesville, Florida, United States
- University of South Florida - Neuromuscular Research, 13330 USF Laurel Drive - Site Number: 8400001 Tampa, Florida, United States
- Columbia University Medical Center - Neurological Institute, 710 W. 168th, 2nd floor, suite 204 - Site Number : 8400003 New York, United States
- Virginia Commonwealth University Medical Center- Site Number : 8400006 Richmond, Virginia, United States
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
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
NCT05481879
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Stanford University Stanford, California, United States
- University of Florida College of Medicine Gainesville, Florida, United States
- Indiana University School of Medicine Indianapolis, Indiana, United States
- University of Iowa Iowa City, Iowa, United States
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
NCT06147414
- Conditions
- Abnormalities, Multiple, Anemia, Anemia, Hemolytic, +78 more
- Locations
-
- Hôpital Cochin, Maternité Port-Royal, service de Gynécologie obstétrique Paris, France
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
NCT07502989
- Conditions
- Congenital Myopathy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Distal Myopathies, +16 more
- Locations
-
- Beth Israel Deaconess Medical Center Boston, Massachusetts, United States
NCT07505342
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Genetic Diseases, Inborn, +11 more
- Locations
-
- University of Rochester Rochester, New York, United States
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
NCT00272883
- Conditions
- Central Core Disease, Centronuclear Myopathy, Congenital Fiber Type Disproportion, +19 more
- Locations
-
- Genetics Division, Boston Children's Hospital Boston, Massachusetts, United States
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
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