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Results for “FKRP”

8 trials

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Showing 8 of 8 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
Early research (Phase 1)Active Not RecruitingNCT05224505
What this trial is testing

ATA-100 (Formerly GNT0006) Gene Therapy Trial in Patients With LGMDR9

Who this might be right for
LGMDR9
Atamyo Therapeutics 6
Not applicableStudy completedNCT00893334
What this trial is testing

Evaluation of Limb-Girdle Muscular Dystrophy

Who this might be right for
Becker Muscular DystrophyLimb-Girdle Muscular Dystrophy, Type 2A (Calpain-3 Deficiency)Limb-Girdle Muscular Dystrophy, Type 2B (Miyoshi Myopathy, Dysferlin Deficiency)+1 more
Cooperative International Neuromuscular Research Group 60
Not applicableUnknownNCT03930628
What this trial is testing

Limb-Girdle Muscular Dystrophy Type 2I in Norway

Who this might be right for
Limb Girdle Muscular Dystrophy, Type 2ILimb Girdle Muscular DystrophyMuscular Dystrophies+1 more
University Hospital of North Norway 106
Testing effectiveness (Phase 2)Looking for participantsNCT05230459
What this trial is testing

Evaluate the Safety of AB-1003 (Previously LION-101) in Subjects With Genetic Confirmation of LGMD2I/R9 (Part1)

Who this might be right for
Limb Girdle Muscular DystrophyLimb-Girdle Muscular Dystrophy Type 2LGMD2I+6 more
AskBio Inc 10
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 applicableStudy completedNCT04202627
What this trial is testing

Biomarker Development in LGMD2i

Who this might be right for
Muscular DystrophiesLimb Girdle Muscular Dystrophy
ML Bio Solutions, Inc. 101
4,000