3 recruiting. .
Follow Muscular Dystrophy, Limb-Girdle, Type 2M: new trials by email Literature Review of Muscular Dystrophy, Limb-Girdle, Type 2M trials Research Report on Muscular Dystrophy, Limb-Girdle, Type 2M
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 |
|---|---|---|---|---|---|---|
| Long-Term Development of Muscular Dystrophy Outcome Assessments LGMD1B, LGMD1C | Recruiting | Virginia Commonwealth University | 1000 | 2023-10-18 | 2025-11-18 | |
| 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 Trial Readiness for the Dystroglycanopathies Muscular Dystrophy | Recruiting | Katherine Mathews | 190 | 2006-04-01 | 2025-07-30 |
Walker-Warburg Syndrome (3) · Muscular Dystrophies (2) · Muscular Dystrophies, Limb-Girdle (2) · Muscular Dystrophy, Limb-Girdle, Type 2G (2) · Muscular Dystrophy, Limb-Girdle, Type 2I (2) · Epilepsy (1) · Intellectual Disability (1) · Limb-Girdle Muscular Dystrophy, Type 1G (1) · Limb-girdle muscular dystrophy type 2A (1) · Limb-girdle muscular dystrophy type 2F (1) · Limb-girdle muscular dystrophy, type 1B (1) · Limb-girdle muscular dystrophy, type 2B (1) · Limb-girdle muscular dystrophy, type 2C (1) · Limb-girdle muscular dystrophy, type 2E (1)
Cobblestone Lissencephaly (3) · Congenital Abnormalities (3) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (3) · Eye Diseases (3) · Eye Diseases, Hereditary (3) · Genetic Diseases, Inborn (3) · Lissencephaly (3) · Malformations of Cortical Development (3) · Malformations of Cortical Development, Group II (3) · Muscular Diseases (3) · Muscular Disorders, Atrophic (3) · Nervous System Diseases (3) · Nervous System Malformations (3) · Heredodegenerative Disorders, Nervous System (2) · Musculoskeletal Diseases (2)
Cure CMD (1) · Katherine Mathews (1) · Virginia Commonwealth University (1)
United States (3)
Gustavo Dziewczapolski, PhD (1) · Katherine Mathews, M.D. (1) · Kevin Campbell, Ph.D. (1) · Nicholas Johnson, MD (1) · Steven A. Moore, M.D. Ph.D. (1)
PMID 20646909, PMID 21220724, PMID 25568299, PMID 26310427, PMID 27872178, PMID 28087826, PMID 29101272, PMID 29759639, PMID 31041397, PMID 32115343, PMID 32764098, PMID 32914449, PMID 33501999, PMID 34857438, PMID 36399172, PMID 37247532, PMID 40245099, PMID 41486779
U54NS053672 (1)