Merosin Deficient Congenital Muscular Dystrophy: Clinical Trials

5 trials for Merosin Deficient Congenital Muscular Dystrophy, newest first

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3 recruiting, 2 completed. 1 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable1Completed 1

Follow Merosin Deficient Congenital Muscular Dystrophy: new trials by email Literature Review of Merosin Deficient Congenital Muscular Dystrophy trials Research Report on Merosin Deficient 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
Characterization of the Natural History of LAMA2-RD and Identification of Novel Disease Biomarkers
Cardiac MRI - LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A), LAMA2-MD \(Merosin Deficient Congenital Muscular Dystrophy, MDC1A\)
RecruitingUniversità Vita-Salute San Raffaele452025-07-312025-08-15
Natural History Study of Children With LAMA2-related Dystrophies
Motor evaluations, Cognitive assessment, Pulmonary function test - Merosin Deficient Congenital Muscular Dystrophy
RecruitingInstitut de Myologie, France402024-12-052024-12-12
Spanish Natural History Study for LAMA2 Muscular Dystrophy
Motor function scales, MUSCLE ULTRASOUND, Muscle Elastography - LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A), Merosin Deficient CMD (Full or Partial)
RecruitingHospital Universitari Vall d'Hebron Research Institute1002021-07-272025-04-11
Retrospective Natural History Study of Infants and Toddlers With LAMA2-CMD
Merosin Deficient Congenital Muscular Dystrophy
CompletedProthelia, Inc.752020-04-242022-02-07
Fat and Glucose Metabolism in Fed and Fasted State in Patients With Low Skeletal Muscle Mass
Fasting - Spinal Muscular Atrophy, Merosin Deficient Congenital Muscular Dystrophy
Not applicableCompletedCopenhagen University Hospital, Rigshospitalet132017-05-292019-05-31

Narrower conditions

Muscular dystrophy congenital, merosin negative (5)  ·  Muscular Atrophy, Spinal (1)  ·  Muscular Dystrophies (1)

Broader conditions

Nervous System Diseases (2)  ·  Neuromuscular Diseases (2)  ·  Central Nervous System Diseases (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Genetic Diseases, Inborn (1)  ·  Motor Neuron Disease (1)  ·  Muscular Diseases (1)  ·  Muscular Disorders, Atrophic (1)  ·  Musculoskeletal Diseases (1)  ·  Neurodegenerative Diseases (1)  ·  Spinal Cord Diseases (1)

Interventions

Angptl4 protein, mouse (1)  ·  Mental Status and Dementia Tests (1)  ·  Nutritional Status (1)  ·  Quality of Life (1)  ·  Respiratory Physiological Phenomena (1)  ·  Respiratory Rate (1)

Sponsors

Copenhagen University Hospital, Rigshospitalet (1)  ·  Hospital Universitari Vall d'Hebron Research Institute (1)  ·  Institut de Myologie, France (1)  ·  Prothelia, Inc. (1)  ·  Università Vita-Salute San Raffaele (1)

Countries

Denmark (1)  ·  France (1)  ·  Italy (1)  ·  Spain (1)  ·  United States (1)

Top investigators

Alan Beggs, PhD (1)  ·  Gustavo Dziewczapolski, PhD (1)  ·  Oscar H Mayer, MD (1)  ·  Rachel Alvarez, BS (1)  ·  Reghan Foley, MD (1)

Results publications

PMID 25307854, PMID 31794464