4 recruiting, 3 unknown, 1 completed. 2 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 2 | Unknown 2 |
Follow Malformations of Cortical Development, Group II: new trials by email Literature Review of Malformations of Cortical Development, Group II trials Research Report on Malformations of Cortical Development, Group II
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 | |
| Functional Tests to Resolve Unsolved Rare Diseases. Rares. Ex-vivo approach concerning 25 patients, In-vitro approach concerning 25 patients - Intellectual Disability, Rubinstein-Taybi Syndrome | Not applicable | Unknown | University Hospital, Bordeaux | 50 | 2023-01-30 | 2024-02-21 |
| 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 | |
| Epilepsy Phenome/Genome Project Epilepsy, Localization-related Epilepsy | Completed | University of California, San Francisco | 4150 | 2007-11-01 | 2018-11-13 | |
| 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) · Epilepsy (3) · Muscular Dystrophies, Limb-Girdle (3) · Muscular Dystrophy, Limb-Girdle, Type 2I (3) · Muscular Dystrophy, Limb-Girdle, Type 2M (3) · Intellectual Disability (2) · Lissencephaly (2) · Muscular Dystrophies (2) · Muscular Dystrophy, Limb-Girdle, Type 2G (2) · Periventricular Nodular Heterotopia (2) · Polymicrogyria (2) · Albinism (1) · Choristoma (1) · Classical Lissencephalies and Subcortical Band Heterotopias (1) · Cognition Disorders (1)
Congenital Abnormalities (8) · Congenital, Hereditary, and Neonatal Diseases and Abnormalities (8) · Nervous System Diseases (8) · Nervous System Malformations (8) · Genetic Diseases, Inborn (7) · Malformations of Cortical Development (7) · Eye Diseases (5) · Eye Diseases, Hereditary (5) · Musculoskeletal Diseases (5) · Brain Diseases (4) · Central Nervous System Diseases (4) · Cobblestone Lissencephaly (4) · Lissencephaly (4) · Muscular Diseases (4)
Phlebotomy (1)
Cure CMD (1) · Harvard University Faculty of Medicine (1) · Katherine Mathews (1) · Newcastle University (1) · Universitair Ziekenhuis Brussel (1) · University Hospital, Bordeaux (1) · University of California, San Francisco (1) · Virginia Commonwealth University (1)
United States (5) · Argentina (1) · Australia (1) · Belgium (1) · France (1) · United Kingdom (1)
Christopher A. Walsh, M.D., Ph.D. (1) · Daniel Lowenstein, MD (1) · Gustavo Dziewczapolski, PhD (1) · Katherine Mathews, M.D. (1) · Kevin Campbell, Ph.D. (1) · Nicholas Johnson, MD (1) · Ruben Kuzniecky, 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 32917807, PMID 33501999, PMID 34857438, PMID 36399172, PMID 37247532, PMID 40245099, PMID 41486779
U54NS053672 (1)