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Results for “LAMA2-related Muscular Dystrophy”

16 trials

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Showing 16 of 16 results

Not applicableLooking for participantsNCT00313677
What this trial is testing

Clinical Trial Readiness for the Dystroglycanopathies

Who this might be right for
Muscular Dystrophy
Katherine Mathews 190
Not applicableWithdrawnNCT01952028
What this trial is testing

LAMA2-related Muscular Dystrophy Brain Study

Who this might be right for
LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A)
Cure CMD
Not applicableStudy completedNCT03970135
What this trial is testing

Fat and Glucose Metabolism in Fed and Fasted State in Patients With Low Skeletal Muscle Mass

Who this might be right for
Spinal Muscular AtrophyMerosin Deficient Congenital Muscular Dystrophy
Rigshospitalet, Denmark 13
Not applicableLooking for participantsNCT06924125
What this trial is testing

Spanish Natural History Study for LAMA2 Muscular Dystrophy

Who this might be right for
LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A)Merosin Deficient CMD (Full or Partial)Merosin Deficient Congenital Muscular Dystrophy+2 more
Hospital Universitari Vall d'Hebron Research Institute 100
Not applicableLooking for participantsNCT06503367
What this trial is testing

Observation Study in Patients Age 0-5 Years With LAMA2-related Congenital Muscular Dystrophy

Who this might be right for
LAMA2-MD \(Merosin Deficient Congenital Muscular Dystrophy, MDC1A\)
Nationwide Children's Hospital 44
Not applicableStudy completedNCT04299321
What this trial is testing

Retrospective Natural History Study of Infants and Toddlers With LAMA2-CMD

Who this might be right for
Merosin Deficient Congenital Muscular Dystrophy
Prothelia, Inc. 75
Not applicableLooking for participantsNCT05394506
What this trial is testing

Modifying Factors in Striated Muscle Laminopathies

Who this might be right for
LaminopathiesEmery Dreifuss Muscular Dystrophy 2LMNA-Related Congenital Muscular Dystrophy+1 more
Institut National de la Santé Et de la Recherche Médicale, France 40
Not applicableLooking for participantsNCT06132750
What this trial is testing

A 5-year Natural History Study in LAMA2-related Muscular Dystrophy and SELENON-related Myopathy.

Who this might be right for
LAMA2-related Muscular DystrophySELENON-related Myopathy
Radboud University Medical Center 40
Not applicableUnknownNCT04020159
What this trial is testing

Global Registry for COL6-related Dystrophies

Who this might be right for
Bethlem MyopathyUllrich Congenital Muscular Dystrophy 1, Digenic, Col6A1/Col6A2Ullrich Congenital Muscular Dystrophy 1, Autosomal Recessive+4 more
Newcastle-upon-Tyne Hospitals NHS Trust 1,000
Not applicableLooking for participantsNCT06354790
What this trial is testing

Natural History Study of Children With LAMA2-related Dystrophies

Who this might be right for
Merosin Deficient Congenital Muscular Dystrophy
Institut de Myologie, France 40
Not applicableNo Longer AvailableNCT05154851
What this trial is testing

HBCMD01- Expanded Access for the Treatment of Congenital Muscular Dystrophy.

Who this might be right for
Congenital Muscular Dystrophy Due to Lamin A/C Mutation
Hope Biosciences Research Foundation
Not applicableStudy completedNCT04478981
What this trial is testing

The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2

Who this might be right for
MDC1ASELENON-related Myopathy
Radboud University Medical Center 38
Testing effectiveness (Phase 2)Study completedNCT01438788
What this trial is testing

Low Protein Diet in Patients With Collagen VI Related Myopathies

Who this might be right for
Bethlem MyopathyUllrich Congenital Muscular Dystrophy
Istituto Ortopedico Rizzoli 8
Not applicableUnknownNCT04001595
What this trial is testing

Global FKRP Registry

Who this might be right for
LGMD2ILGMDR9Limb Girdle Muscular Dystrophy+4 more
Newcastle University 1,000
Not applicableLooking for participantsNCT01403402
What this trial is testing

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Who this might be right for
Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) DeficiencyAlpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)+49 more
Cure CMD
Not applicableLooking for participantsNCT07125040
What this trial is testing

Characterization of the Natural History of LAMA2-RD and Identification of Novel Disease Biomarkers

Who this might be right for
LAMA2-MD (Merosin Deficient Congenital Muscular Dystrophy, MDC1A)LAMA2-MD \(Merosin Deficient Congenital Muscular Dystrophy, MDC1A\)Merosin Deficient CMD (Full or Partial)+1 more
Università Vita-Salute San Raffaele 45
4,000