Miyoshi myopathy: Clinical Trials

6 trials for Miyoshi myopathy, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

3 completed, 1 enrolling by invitation, 1 unknown, 1 withdrawn. 1 Phase 2, 1 Phase 3.

By phase and status

PhaseTrialsStatus
Phase 21Completed 1
Phase 31Completed 1

Follow Miyoshi myopathy: new trials by email Literature Review of Miyoshi myopathy trials Research Report on Miyoshi myopathy

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
Clinical, Immunological, Morphological and Genetic Characteristics of Patients With Dysferlinopathy (LGMD R2) in the RF
Dysferlinopathy, Miyoshi Myopathy
Enrolling by invitationArtgen Biotech1002020-01-152025-06-27
Clinical Outcome Study for Dysferlinopathy
Dysferlinopathy, LGMD2B Now Classified as LGMDR2
UnknownNewcastle-upon-Tyne Hospitals NHS Trust2002012-09-012022-07-26
Dysferlinopathy Protein in Peripheral Blood Monocytes.
Protein analysis - Muscular Dystrophies, Limb-Girdle Muscular Dystrophy Type 2B
CompletedFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau1492012-02-012024-07-18
Evaluation of Limb-Girdle Muscular Dystrophy
Becker Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Type 2A (Calpain-3 Deficiency)
CompletedCooperative International Neuromuscular Research Group602009-04-012014-03-07
Genetic Study of Familial and Sporadic ALS/Motor Neuron Disease, Miyoshi Myopathy and Other Neuromuscular Disorders
Amyotrophic Lateral Sclerosis, Frontotemporal Dementia
WithdrawnUniversity of Massachusetts, Worcester2009-01-012024-09-19
Deflazacort in Dysferlinopathies
deflazacort, placebo - LGMD2B, Miyoshi Myopathy
Phase 2 / Phase 3CompletedLudwig-Maximilians - University of Munich252003-09-012015-09-02

Narrower conditions

Muscular Dystrophies (5)  ·  Limb-girdle muscular dystrophy, type 2B (4)  ·  Dysferlinopathy (3)  ·  Amyotrophic Lateral Sclerosis (1)  ·  Amyotrophic lateral sclerosis 1 (1)  ·  Frontotemporal Dementia (1)  ·  Motor Neuron Disease (1)  ·  Muscular Dystrophies, Limb-Girdle (1)  ·  Muscular Dystrophy, Duchenne (1)  ·  Myopathy, Distal, with Anterior Tibial Onset (1)

Broader conditions

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (5)  ·  Genetic Diseases, Inborn (5)  ·  Muscular Diseases (5)  ·  Muscular Disorders, Atrophic (5)  ·  Musculoskeletal Diseases (5)  ·  Nervous System Diseases (5)  ·  Neuromuscular Diseases (5)  ·  Brain Diseases (1)  ·  Central Nervous System Diseases (1)  ·  Dementia (1)  ·  Frontotemporal Lobar Degeneration (1)  ·  Genetic Diseases, X-Linked (1)  ·  Mental Disorders (1)  ·  Metabolic Diseases (1)  ·  Neurocognitive Disorders (1)

Interventions

Adrenal Cortex Hormones (1)  ·  deflazacort (1)

Sponsors

Artgen Biotech (1)  ·  Cooperative International Neuromuscular Research Group (1)  ·  Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau (1)  ·  Ludwig-Maximilians - University of Munich (1)  ·  Newcastle-upon-Tyne Hospitals NHS Trust (1)  ·  University of Massachusetts, Worcester (1)

Countries

United States (3)  ·  Spain (2)  ·  Chile (1)  ·  Denmark (1)  ·  France (1)  ·  Germany (1)  ·  Italy (1)  ·  Japan (1)  ·  Russia (1)  ·  South Korea (1)  ·  United Kingdom (1)

Top investigators

Carolina Tesi-Rocha, M.D. (1)  ·  Maggie C. Walter, MD (1)  ·  Meredith K James (1)  ·  Robert H Brown Jr., D Phil,MD (1)  ·  Roman Deev, PhD (1)  ·  Susan Sparks, M.D., Ph.D. (1)  ·  Volker Straub (1)

Results publications

PMID 19251627, PMID 19734901, PMID 20582942, PMID 20685689, PMID 20801717, PMID 21438137, PMID 22801503, PMID 23152587, PMID 23406536, PMID 29378789, PMID 29735511, PMID 30626655, PMID 35047756, PMID 37553796, PMID 38365661, PMID 39973465