4 recruiting, 2 unknown. 1 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Unknown 1 |
Follow Lissencephaly: new trials by email Literature Review of Lissencephaly trials Research Report on Lissencephaly
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 | |
| Combining Exome and Transcriptome Data to Unravel the Genetic Basis of the Lissencephalies Venipuncture and skin biopsy for RNA extraction - Classical Lissencephalies and Subcortical Band Heterotopias | Not applicable | Unknown | Universitair Ziekenhuis Brussel | 50 | 2022-01-01 | 2022-01-11 |
| Global FKRP Registry Patient Registry - LGMD2I, LGMDR9 | Unknown | Newcastle University | 1000 | 2013-11-01 | 2024-01-30 | |
| 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 | |
| Human Epilepsy Genetics--Neuronal Migration Disorders Study Brain Malformation, Neuronal Migration Disorder | Recruiting | Harvard University Faculty of Medicine | 3500 | 1996-04-01 | 2023-09-21 |
Walker-Warburg Syndrome (4) · Muscular Dystrophies, Limb-Girdle (3) · Muscular Dystrophy, Limb-Girdle, Type 2I (3) · Muscular Dystrophy, Limb-Girdle, Type 2M (3) · Epilepsy (2) · Muscular Dystrophies (2) · Muscular Dystrophy, Limb-Girdle, Type 2G (2) · Choristoma (1) · Classical Lissencephalies and Subcortical Band Heterotopias (1) · Cognition Disorders (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)
Congenital Abnormalities (6) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (6) · Malformations of Cortical Development (6) · Nervous System Diseases (6) · Nervous System Malformations (6) · Genetic Diseases, Inborn (5) · Malformations of Cortical Development, Group II (5) · Cobblestone Lissencephaly (4) · Eye Diseases (4) · Eye Diseases, Hereditary (4) · Muscular Diseases (4) · Muscular Disorders, Atrophic (4) · Musculoskeletal Diseases (4) · Neuromuscular Diseases (3)
Phlebotomy (1)
Cure CMD (1) · Harvard University Faculty of Medicine (1) · Katherine Mathews (1) · Newcastle University (1) · Universitair Ziekenhuis Brussel (1) · Virginia Commonwealth University (1)
United States (4) · Belgium (1) · United Kingdom (1)
Christopher A. Walsh, M.D., Ph.D. (1) · 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) · Volker Straub, MD, PhD (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)