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Results for “Hereditary Muscular Dystrophy”

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Showing 20 of 0 results

Testing effectiveness (Phase 2)Study completedNCT03218995
What this trial is testing

Study of Eteplirsen in Young Participants With Duchenne Muscular Dystrophy (DMD) Amenable to Exon 51 Skipping

Who this might be right for
Duchenne Muscular Dystrophy
Sarepta Therapeutics, Inc. 15
Large-scale testing (Phase 3)Study completedNCT01603407
What this trial is testing

Finding the Optimum Regimen for Duchenne Muscular Dystrophy

Who this might be right for
Duchenne Muscular Dystrophy
University of Rochester 196
Not applicableNot Yet RecruitingNCT06732011
What this trial is testing

Evaluation of Brain Dysfunction in Patients with Duchene Muscular Dystrophy

Who this might be right for
Duchenne Muscular Dystrophy
Assiut University 42
Testing effectiveness (Phase 2)Ended earlyNCT02606136
What this trial is testing

Trial of Pamrevlumab (FG-3019), in Non-Ambulatory Participants With Duchenne Muscular Dystrophy (DMD)

Who this might be right for
Duchenne Muscular Dystrophy
Kyntra Bio 21
Not applicableStudy completedNCT04018820
What this trial is testing

Effects of a 12-week Strength Training Program in Men With Myotonic Dystrophy Type 1

Who this might be right for
Myotonic Dystrophy 1
Élise Duchesne 11
Not applicableStudy completedNCT01689480
What this trial is testing

Prospective Study for 24-months of Physical Training Introduced in Lifestyle of Patients With FSHD : Tolerance, Sustainability and Efficiency of Unsupervised Training Program.

Who this might be right for
Muscular Dystrophy, Facioscapulohumeral
Centre Hospitalier Universitaire de Saint Etienne 15
Testing effectiveness (Phase 2)Ended earlyNCT00847379
What this trial is testing

Phase 2B Extension Study of Ataluren (PTC124) in Duchenne/Becker Muscular Dystrophy (DMD/BMD)

Who this might be right for
Duchenne Muscular DystrophyBecker Muscular Dystrophy
PTC Therapeutics 173
Early research (Phase 1)Ended earlyNCT06747273
What this trial is testing

Study to Evaluate the Safety, Tolerability, and Efficacy of SRP-9004 Administered by Systemic Infusion in Limb Girdle Muscular Dystrophy Type 2D/R3 Participants in the United States

Who this might be right for
Limb Girdle Muscular DystrophyLimb Girdle Muscular Dystrophy Type 2D/R3
Sarepta Therapeutics, Inc. 4
Not applicableLooking for participantsNCT00874783
What this trial is testing

Development of IPS from Donated Somatic Cells of Patients with Neurological Diseases

Who this might be right for
Neurodegenerative Disorders
Hadassah Medical Organization 120
Testing effectiveness (Phase 2)Study completedNCT02603562
What this trial is testing

Evaluate Safety and Biological Activity of ATYR1940 in Participants With Early Onset Facioscapulohumeral Muscular Dystrophy

Who this might be right for
Facioscapulohumeral Muscular Dystrophy (FSHD)
aTyr Pharma, Inc. 8
Not applicableActive Not RecruitingNCT05429736
What this trial is testing

Activating Spinal Circuits to Improve Walking, Balance, Strength, and Reduce Spasticity

Who this might be right for
Incomplete Spinal Cord InjurySpasticity, Muscle
Shepherd Center, Atlanta GA 28
Testing effectiveness (Phase 2)Active Not RecruitingNCT04433234
What this trial is testing

Long-term, Extension Study of DS-5141b in Patients With Duchenne Muscular Dystrophy

Who this might be right for
Duchenne Muscular Dystrophy
Daiichi Sankyo Co., Ltd. 8
Large-scale testing (Phase 3)Study completedNCT01557400
What this trial is testing

Study of Ataluren for Previously Treated Participants With Nonsense Mutation Duchenne/Becker Muscular Dystrophy (nmDBMD) in Europe, Israel, Australia, and Canada

Who this might be right for
Duchenne Muscular DystrophyBecker Muscular DystrophyDystrophinopathy
PTC Therapeutics 94
Early research (Phase 1)Study completedNCT02383511
What this trial is testing

Modified Diet Trial: A Study of SMT C1100 in Paediatric Patients With DMD Who Follow a Balanced Diet

Who this might be right for
Muscular Dystrophy, Duchenne
Summit Therapeutics 12
Not applicableWithdrawnNCT03161847
What this trial is testing

Natural History Study of Oculopharyngeal Muscular Dystrophy

Who this might be right for
Oculopharyngeal Muscular Dystrophy
University of New Mexico
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
Large-scale testing (Phase 3)Looking for participantsNCT05004129
What this trial is testing

Safety and Efficacy of Tideglusib in Congenital or Childhood Onset Myotonic Dystrophy

Who this might be right for
Congenital Myotonic Dystrophy
AMO Pharma Limited 76
Not applicableLooking for participantsNCT01484678
What this trial is testing

Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy

Who this might be right for
Duchenne Muscular DystrophyBecker Muscular Dystrophy
University of Florida 550
Not applicableNot Yet RecruitingNCT06579859
What this trial is testing

Development of a Registry to Assess Natural History in Duchenne Muscular Dystrophy

Who this might be right for
Duchenne Muscular Dystrophy
Fondazione Policlinico Universitario Agostino Gemelli IRCCS 200
Not applicableStudy completedNCT02729597
What this trial is testing

Tracking the Brain in Myotonic Dystrophies: a 5-year Longitudinal Follow-up Study

Who this might be right for
Myotonic Dystrophy 1Myotonic Dystrophy 2
University Hospital, Bonn 49
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