Clinical Trials on Muscular Dystrophy, Emery-Dreifuss

Total 731 results

Institut National de la Santé Et de la Recherche...

Recruiting

Modifying Factors in Striated Muscle Laminopathies (LMNAModifier)

Laminopathies | Emery Dreifuss Muscular Dystrophy 2 | LMNA-Related Congenital Muscular Dystrophy | Dilated Cardiomyopathy-1A

France
Pitié-Salpêtrière Hospital

Recruiting

Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies) (OPALE)

Laminopathies | Emerinopathies

France
Cure CMD

Recruiting

Congenital Muscle Disease Study of Patient and Family Reported Medical Information (CMDPROS)

Emery-Dreifuss Muscular Dystrophy | Congenital Myasthenic Syndrome | Limb-Girdle Muscular Dystrophy | Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency | Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy) and other conditions

United States
Myotonic Dystrophy Foundation

Recruiting

Myotonic Dystrophy Family Registry (MDFR)

Myotonic Dystrophy | Myotonic Dystrophy 1 | Steinert's Disease | Congenital Myotonic Dystrophy | PROMM (Proximal Myotonic Myopathy) | Steinert Disease | Dystrophia Myotonica 1 | Myotonic Dystrophy 2 | Dystrophia Myotonica | Dystrophia Myotonica 2 | Myotonia Dystrophica | Myotonic Dystrophy, Congenital | Myotonic... and other conditions

United States
University Hospital, Montpellier

Unknown

Endomysial Fibrosis, Muscular Inflammatory Response and Calcium Homeostasis Dysfunction in Duchenne Muscular Dystrophy

Duchenne Muscular Distrophy (DMD)

France
Avidity Biosciences, Inc.

Recruiting

Phase 1/2 Study of AOC 1020 in Adults With Facioscapulohumeral Muscular Dystrophy (FSHD) (FORTITUDE)

Muscular Dystrophies | Muscular Dystrophy, Facioscapulohumeral | FSHD | Facio-Scapulo-Humeral Dystrophy | FMD | Facioscapulohumeral Muscular Dystrophy 1 | FSHD2 | FSHD1 | FMD2 | Fascioscapulohumeral Muscular Dystrophy | Fascioscapulohumeral Muscular Dystrophy Type 1 | Fascioscapulohumeral Muscular Dystrophy... and other conditions

United States, United Kingdom, Canada
Wyeth is now a wholly owned subsidiary of Pfizer

Completed

Study Evaluating MYO-029 in Adult Muscular Dystrophy

Becker Muscular Dystrophy | Facioscapulohumeral Muscular Dystrophy | Limb-Girdle Muscular Dystrophy

United States
Massachusetts General Hospital
University of Pittsburgh; Boston Children's Hospital; Brigham and Women's Hospital and other collaborators

Recruiting

Biomarker Development for Muscular Dystrophies

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy | Myotonic Dystrophy | Facioscapulohumeral Muscular Dystrophy

United States
University of North Carolina, Chapel Hill
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) and other collaborators

Completed

Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy

Muscular Dystrophies | Duchenne Muscular Dystrophy | Becker Muscular Dystrophy | Limb-Girdle Muscular Dystrophy

United States
Boston Children's Hospital
National Institute of Neurological Disorders and Stroke (NINDS)

Recruiting

Molecular Analysis of Patients With Neuromuscular Disease

Limb-girdle Muscular Dystrophy | Neuromuscular; Disorder, Hereditary | Duchenne/Becker Muscular Dystrophy

United States
University of Rochester
National Institute of Neurological Disorders and Stroke (NINDS)

Recruiting

Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry

Muscular Dystrophy | Myotonic Dystrophy Type 2 | Myotonic Dystrophy Type 1 | Myotonic Dystrophy | Facioscapulohumeral Muscular Dystrophy | Steinert's Disease | Congenital Myotonic Dystrophy | PROMM (Proximal Myotonic Myopathy) | Myotonic Muscular Dystrophy

United States
Rigshospitalet, Denmark

Completed

Muscle MRI in Becker Muscular Dystrophy and in Limb-girdle Muscular Dystrophy Type 2I

Becker Muscular Dystrophy | Limb-Girdle Muscular Dystrophy Type 2I

Denmark
University Hospital of North Norway
University of Tromso; Norwegian Muscle Disease Association (FFM); Norwegian National... and other collaborators

Active, not recruiting

Limb-Girdle Muscular Dystrophy Type 2I in Norway

Muscular Dystrophies | Limb Girdle Muscular Dystrophy | Limb Girdle Muscular Dystrophy, Type 2I | Limb Girdle Muscular Dystrophy R9 FKRP-related

Norway
Laurent Servais
SYSNAV

Recruiting

Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study

Duchenne Muscular Dystrophy | Fascioscapulohumeral Muscular Dystrophy

Belgium
Virginia Commonwealth University
Edgewise Therapeutics, Inc.

Recruiting

Defining Endpoints in Becker Muscular Dystrophy (GRASP-01-002)

Muscular Dystrophies | Becker Muscular Dystrophy | Muscular Dystrophy in Children | Muscular Dystrophy, Becker

United States, United Kingdom
Massachusetts General Hospital

Completed

Safety, Tolerability and Effects of L-Arginine in Boys With Dystrophinopathy on Corticosteroids

Duchenne Muscular Dystrophy | Dystrophinopathy | Becker's Muscular Dystrophy

United States
Cooperative International Neuromuscular Research...
National Institutes of Health (NIH)

Completed

Cardiac Magnetic Resonance in Children With Muscular Dystrophy

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy | Limb Girdle Muscular Dystrophy

United States
Cooperative International Neuromuscular Research...
United States Department of Defense

Completed

Clinical Trial of Coenzyme Q10 and Lisinopril in Muscular Dystrophies

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy | Limb Girdle Muscular Dystrophy

United States, Japan, Canada
Cooperative International Neuromuscular Research...
National Institutes of Health (NIH)

Completed

Cardiac Outcome Measures in Children With Muscular Dystrophy

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy | Limb Girdle Muscular Dystrophy

United States
Politecnico di Milano
IRCCS Eugenio Medea; Villa Beretta Rehabilitation Center

Completed

User-centred Assistive System for Arm Functions in Neuromuscular Subjects (USEFUL)

Muscular Dystrophies | Muscular Dystrophy, Duchenne | Muscular Dystrophy, Becker | Muscular Dystrophy, Limb-Girdle Type 2

Italy
Cooperative International Neuromuscular Research...
Carolinas Medical Center lead study site

Completed

Evaluation of Limb-Girdle Muscular Dystrophy

Becker Muscular Dystrophy | Limb-Girdle Muscular Dystrophy, Type 2A (Calpain-3 Deficiency) | Limb-Girdle Muscular Dystrophy, Type 2B (Miyoshi Myopathy, Dysferlin Deficiency) | Limb-Girdle Muscular Dystrophy, Type 2I (FKRP-deficiency)

United States
Centre Hospitalier Universitaire de Nice

Recruiting

Study to Evaluate the Efficacy and Safety of Satralizumab in FSHD1 (REINFORCE)

Facioscapulohumeral Muscular Dystrophy 1

France, Canada
Hoffmann-La Roche

Recruiting

A Study to Evaluate RO7204239 in Participants With Facioscapulohumeral Muscular Dystrophy (MANOEUVRE)

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, Denmark, United Kingdom, Italy
Fulcrum Therapeutics

Active, not recruiting

Efficacy and Safety of Losmapimod in Treating Participants With Facioscapulohumeral Muscular Dystrophy (FSHD) (REACH)

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, Spain, Italy, Denmark, Canada, Germany, France, Netherlands, United Kingdom
Fulcrum Therapeutics

Active, not recruiting

Efficacy and Safety of Losmapimod in Treating Subjects With Facioscapulohumeral Muscular Dystrophy (FSHD) With Open-Label Extension (OLE)

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, Canada, France, Spain
Fulcrum Therapeutics

Completed

Efficacy and Safety of Losmapimod in Subjects With Facioscapulohumeral Muscular Dystrophy (FSHD) (FSHD)

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, Canada, France, Spain
Avidity Biosciences, Inc.

Completed

Study of AOC 1001 in Adult Myotonic Dystrophy Type 1 (DM1) Patients (MARINA)

Myotonic Dystrophy | Myotonic Disorders | Myotonic Dystrophy Type 1 (DM1) | Myotonic Dystrophy 1 | Myotonic Muscular Dystrophy | DM1 | Dystrophy Myotonic | Steinert Disease

United States
Northwestern University

Completed

Weekly Steroids in Muscular Dystrophy (WSiMD)

Becker Muscular Dystrophy | Limb-girdle Muscular Dystrophy

United States
Centre Hospitalier Universitaire de Nice

Recruiting

New Clinical Outcome Measures to Remotely Evaluate Patients With FacioScapuloHumeral Muscular Dystrophy (PROGRESS-FSHD)

Type 1 Facioscapulohumeral Muscular Dystrophy

France
aTyr Pharma, Inc.

Completed

Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Participants With Muscular Dystrophy

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, Netherlands, France, Italy
Grete Andersen, MD

Completed

High Intensity Training in Patients With Facioscapulohumeral Muscular Dystrophy (HIT-FSHD)

FSHD - Facioscapulohumeral Muscular Dystrophy

Denmark
aTyr Pharma, Inc.

Completed

Evaluate Safety and Biological Activity of ATYR1940 in Participants With Early Onset Facioscapulohumeral Muscular Dystrophy (FSHD)

Facioscapulohumeral Muscular Dystrophy (FSHD)

United States, France, Italy
Fulcrum Therapeutics

Active, not recruiting

Evaluation of Safety, Tolerability, and Changes in Biomarker and Clinical Outcome Assessments of Losmapimod for FSHD1 With Extension (FSHD)

Facioscapulohumeral Muscular Dystrophy 1

Netherlands
Allergy and Asthma Consultants, Wichita, Kansas
Aidan Foundation; Neil H. Riordan PhD

Completed

Allogeneic Human Umbilical Cord Mesenchymal Stem Cells for a Single Male Patient With Duchenne Muscular Dystrophy (DMD)

Duchenne's Muscular Dystrophy

United States
RSPR Pharma AB

Completed

CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

Sweden
National Institute of Neurological Disorders and...

Completed

Gentamicin Treatment of Muscular Dystrophy

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
Canan İpek

Unknown

Effects of Fear of Falling on Physical Performance and Quality of Life in Children With Duchenne Muscular Dystrophy

Neuromuscular Diseases | Duchenne Muscular Dystrophy | Dystrophy | Dystrophy, Muscular

Turkey
Arrowhead Pharmaceuticals

Recruiting

Study of ARO-DUX4 in Adult Patients With Facioscapulohumeral Muscular Dystrophy Type 1

Facio-Scapulo-Humeral Dystrophy

New Zealand
ML Bio Solutions, Inc.

Recruiting

Study to Evaluate the Efficacy and Safety of BBP-418 (Ribitol) in Patients With Limb Girdle Muscular Dystrophy 2I (LGMD2I) (Fortify)

Limb-Girdle Muscular Dystrophy Type 2I (LGMD2I)

United States, Netherlands, United Kingdom, Norway, Italy, Denmark, Australia
Linda Pax Lowes

Recruiting

Natural History of Limb Girdle Muscular Dystrophy Type 2A and Type 2E

Limb-Girdle Muscular Dystrophy Type 2A | Limb-Girdle Muscular Dystrophy, Type 2E

United States
CureDuchenne

Recruiting

CureDuchenne Link®: A Resource for Research (CDLink)

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
The Duchenne Registry
Parent Project Muscular Dystrophy

Recruiting

The Duchenne Registry

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
University Hospital, Montpellier

Unknown

Evaluation of Muscle miRNA as Biomarkers in Dystrophinopathies (biodystromirs)

Muscular Dystrophies | Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

France
aTyr Pharma, Inc.

Completed

Study to Evaluate the Long-Term Safety, Tolerability, and Biological Activity of ATYR1940 in Participants With Limb Girdle and Facioscapulohumeral Muscular Dystrophy (FSHD) (FSHD)

Facioscapulohumeral Muscular Dystrophy | Limb Girdle Muscular Dystrophy

United States, Denmark, Italy
Newcastle-upon-Tyne Hospitals NHS Trust

Recruiting

Global Registry for COL6-related Dystrophies

Bethlem Myopathy | Ullrich Congenital Muscular Dystrophy 1, Digenic, Col6A1/Col6A2 | Ullrich Congenital Muscular Dystrophy 1, Autosomal Recessive | Ullrich Congenital Muscular Dystrophy 1, Autosomal Dominant | Bethlem Myopathy 1, Autosomal Recessive | UCMD | BTHLM1

United Kingdom
Rigshospitalet, Denmark

Not yet recruiting

Follow-up Study on Female Carriers With DMD Gene Variants

Muscular Dystrophy | Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

Denmark
Ning Wang, MD., PhD.

Recruiting

A Registered Cohort Study on FSHD1

Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)

China
Nationwide Children's Hospital
Parent Project Muscular Dystrophy

Recruiting

Characterization of Clinical Skeletal and Cardiac Impairment in Carriers of DMD and BMD

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
University of Florida
Children's Hospital of Philadelphia; National Institute of Arthritis and Musculoskeletal... and other collaborators

Recruiting

Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

United States
Catholic University, Italy

Unknown

Ramipril Versus Carvedilol in Duchenne and Becker Patients

Duchenne Muscular Dystrophy | Becker Muscular Dystrophy

Italy

Clinical Trials on Muscular Dystrophy, Emery-Dreifuss

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