4 completed, 1 recruiting, 1 withdrawn. 1 Not applicable.
| Phase | Trials | Status |
|---|---|---|
| Not applicable | 1 | Completed 1 |
Follow Cure CMD: new trials by email
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 |
|---|---|---|---|---|---|---|
| Retrospective Natural History Study of Infants and Toddlers With LAMA2-CMD Merosin Deficient Congenital Muscular Dystrophy | Completed | Prothelia, Inc. | 75 | 2020-04-24 | 2022-02-07 | |
| LAMA2-related Muscular Dystrophy Brain Study LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A) | Withdrawn | Cure CMD | 2013-11-01 | 2018-03-07 | ||
| A Study to Test Lung Stretch Therapy (Hyperinsufflation) in Children With Collagen VI Muscular Dystrophy Hyperinsufflation therapy - Congenital Muscular Dystrophy | Not applicable | Completed | Children's Hospital Medical Center, Cincinnati | 34 | 2013-04-01 | 2016-07-26 |
| Myotubular Myopathy Event Study X-linked Myotubular Myopathy | Completed | Cure CMD | 33 | 2013-04-01 | 2018-03-07 | |
| Myotubular Myopathy Genetic Testing Study Genetic Testing - Myotubular Myopathy | Completed | Cure CMD | 23 | 2013-03-01 | 2018-03-07 | |
| 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 |
Muscular dystrophy congenital, merosin negative (2) · Myopathies, Structural, Congenital (2) · Myotonia Congenita (2) · Epilepsy (1) · Intellectual Disability (1) · Muscular Dystrophies, Limb-Girdle (1) · Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency (1) · Muscular Dystrophy, Emery-Dreifuss (1) · Muscular Dystrophy, Limb-Girdle, Type 2G (1) · Muscular Dystrophy, Limb-Girdle, Type 2M (1) · Musculoskeletal Diseases (1) · Myasthenic Syndromes, Congenital (1) · Neuromuscular Diseases (1) · Respiratory Aspiration (1) · Seizures (1)
Base Sequence (1) · Genetic Testing (1)
United States (6)
Gustavo Dziewczapolski, PhD (2) · Alan Beggs, PhD (1) · Anne Rutkowski, MD (1) · Anne Rutkowski, MD, PhD (1) · Elizabeth DeChene, MS, GCG (1) · James Dowling, MD, PhD (1) · Joseph Hornyak, MD, PhD (1) · Oscar H Mayer, MD (1) · Rachel Alvarez, BS (1) · Raouf S Amin, MD (1) · Reghan Foley, MD (1) · Sabine de Chastonay, PhD (1) · Soma Das, PhD (1)
PMID 20434914, PMID 25307854, PMID 31794464
R34HL113390 (1)