3 completed, 3 recruiting. 2 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 2 | Completed 1, Recruiting 1 |
Follow Muscular Dystrophy, Emery-Dreifuss: new trials by email Literature Review of Muscular Dystrophy, Emery-Dreifuss trials Research Report on Muscular Dystrophy, Emery-Dreifuss
Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.
| Trial | Phase | Status | Sponsor | Enrollment | Start | Updated |
|---|---|---|---|---|---|---|
| Modifying Factors in Striated Muscle Laminopathies Skin Biopsy, Muscle biopsy - Laminopathies, Emery Dreifuss Muscular Dystrophy 2 | Not applicable | Recruiting | Institut National de la Santé Et de la Recherche Médicale, France | 40 | 2022-09-08 | 2026-03-04 |
| Changes of Motor Function Tests in Congenital Myopathy Subjects Treated With Oral Salbutamol as Compared to no Treatment Salbutamol (as Salbutamol Sulfate) 2 Mg Oral Tablet, Salbutamol Only Product in Oral Dose Form - Congenital Myopathy, Neuromuscular Diseases | Not applicable | Completed | Vastra Gotaland Region | 18 | 2021-10-25 | 2025-06-19 |
| A Model for Healthy Aging: Moscow Centenarians (AGE-100) Aging | Completed | Pirogov Russian National Research Medical University | 100 | 2016-10-01 | 2021-03-23 | |
| Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies) Laminopathies, Emerinopathies | Recruiting | Pitié-Salpêtrière Hospital | 800 | 2013-07-11 | 2026-09-21 | |
| Congenital Muscle Disease Study of Patient and Family Reported Medical Information Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency, Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy) | Recruiting | Cure CMD | 4000 | 2009-09-01 | 2021-08-09 | |
| Clinical Studies of Progeria Progeria | Completed | National Human Genome Research Institute (NHGRI) | 15 | 2004-10-14 | 2019-11-15 |
Autosomal Emery-Dreifuss Muscular Dystrophy (4) · Laminopathies (2) · Musculoskeletal Diseases (2) · Myotonia Congenita (2) · Neuromuscular Diseases (2) · Aging, Premature (1) · Atherosclerosis (1) · Cardiomyopathy, Dilated (1) · Epilepsy (1) · Intellectual Disability (1) · Lipodystrophy (1) · Muscular Dystrophies (1) · Muscular Dystrophies, Limb-Girdle (1) · Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency (1)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities (6) · Genetic Diseases, Inborn (6) · Muscular Diseases (6) · Muscular Disorders, Atrophic (6) · Nervous System Diseases (6) · Muscular Dystrophies (5) · Musculoskeletal Diseases (4) · Neuromuscular Diseases (4) · Genetic Diseases, X-Linked (3) · Cardiovascular Diseases (2) · Heredodegenerative Disorders, Nervous System (2) · Laminopathies (2) · Myotonic Disorders (2) · Neurodegenerative Diseases (2)
Albuterol (1) · Dosage Forms (1) · Tablets (1)
Cure CMD (1) · Institut National de la Santé Et de la Recherche Médicale, France (1) · National Human Genome Research Institute (NHGRI) (1) · Pirogov Russian National Research Medical University (1) · Pitié-Salpêtrière Hospital (1) · Vastra Gotaland Region (1)
France (2) · United States (2) · Russia (1) · Sweden (1)
Gisele Bonne, PhD (1) · Gustavo Dziewczapolski, PhD (1) · Karim Wahbi, MD, PhD (1) · Niklas Darin, M.D (1) · Olga N. Tkacheva, Professor (1) · Rabah Ben Yaou, MD (1) · William A Gahl, M.D. (1)
PMID 18256394, PMID 31155932, PMID 41790128
2019 (1)