Congenital Muscular Dystrophy: Clinical Trials

6 trials for Congenital Muscular Dystrophy, newest first

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3 completed, 2 recruiting, 1 unknown. 2 Not applicable, 1 Phase 1, 1 Phase 4.

By phase and status

PhaseTrialsStatus
Not applicable2Completed 1, Recruiting 1
Phase 11Completed 1
Phase 41Completed 1

Follow Congenital Muscular Dystrophy: new trials by email Literature Review of Congenital Muscular Dystrophy trials Research Report on Congenital Muscular Dystrophy

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study
ActiMyo/Syde - Duchenne Muscular Dystrophy, Fascioscapulohumeral Muscular Dystrophy
Not applicableRecruitingCentre Hospitalier Universitaire de Liege3002020-07-102025-05-20
Swiss Registry for Neuromuscular Disorders
SMA, DMD
RecruitingUniversity of Bern20002018-06-202026-01-15
Congenital Muscular Dystrophy Ascending Multiple Dose Cohort Study Analyzing Pharmacokinetics at Three Dose Levels In Children and Adolescents With Assessment of Safety and Tolerability of Omigapil (CALLISTO)
Omigapil - Congenital Muscular Dystrophy
Phase 1CompletedSanthera Pharmaceuticals202014-12-012021-09-24
Global FKRP Registry
Patient Registry - LGMD2I, LGMDR9
UnknownNewcastle University10002013-11-012024-01-30
A Study to Test Lung Stretch Therapy (Hyperinsufflation) in Children With Collagen VI Muscular Dystrophy
Hyperinsufflation therapy - Congenital Muscular Dystrophy
Not applicableCompletedChildren's Hospital Medical Center, Cincinnati342013-04-012016-07-26
Flu Vaccine Study in Neuromuscular Patients 2011
2011-2012 seasonal flu vaccine Subcutaneous, 2011-2012 seasonal flu vaccine Intramuscular - Duchenne Muscular Dystrophy, Spinal Muscular Atrophy
Phase 4CompletedChildren's Hospital Medical Center, Cincinnati222011-08-012020-10-19

Narrower conditions

Muscular Dystrophy, Duchenne (2)  ·  Charcot-Marie-Tooth Disease (1)  ·  Influenza, Human (1)  ·  Muscular Atrophy, Spinal (1)  ·  Muscular Dystrophies, Limb-Girdle (1)  ·  Muscular Dystrophy, Facioscapulohumeral (1)  ·  Muscular Dystrophy, Limb-Girdle, Type 2I (1)  ·  Myopathies, Structural, Congenital (1)  ·  Myotonic Dystrophy (1)  ·  Walker-Warburg Syndrome (1)

Broader conditions

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (3)  ·  Genetic Diseases, Inborn (3)  ·  Muscular Diseases (3)  ·  Muscular Disorders, Atrophic (3)  ·  Muscular Dystrophies (3)  ·  Musculoskeletal Diseases (3)  ·  Nervous System Diseases (3)  ·  Neuromuscular Diseases (3)  ·  Congenital Abnormalities (2)  ·  Genetic Diseases, X-Linked (2)  ·  Nervous System Malformations (2)  ·  Neurodegenerative Diseases (2)  ·  Central Nervous System Diseases (1)  ·  Cobblestone Lissencephaly (1)  ·  Eye Diseases (1)

Interventions

Influenza Vaccines (1)  ·  dibenzo(b,f)oxepin-10-ylmethyl-methyl-prop-2-ynyl-amine (1)

Sponsors

Children's Hospital Medical Center, Cincinnati (2)  ·  Centre Hospitalier Universitaire de Liege (1)  ·  Newcastle University (1)  ·  Santhera Pharmaceuticals (1)  ·  University of Bern (1)

Countries

United States (2)  ·  Belgium (1)  ·  Czechia (1)  ·  Egypt (1)  ·  Hungary (1)  ·  Poland (1)  ·  Romania (1)  ·  Slovenia (1)  ·  Switzerland (1)  ·  United Kingdom (1)

Top investigators

Brenda Wong, MD (1)  ·  Claudia E Kuehni, Prof. MD (1)  ·  Raouf S Amin, MD (1)  ·  Volker Straub, MD, PhD (1)

Results publications

PMID 38915423

NIH funding

2018 (1), R34HL113390 (1)