Current Projects

Every day Muscular Dystrophy UK is working towards a future with effective treatments and ultimately cures for all muscle-wasting and associated neuromuscular conditions. Learn about the research projects that we are currently funding.

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New concepts for the treatment of mitochondrial myopathies
Developing advanced molecular patch therapy for collagen VI-related congenital muscular dystrophy
Understanding the impact of additional genes in animal models of LAMA2-related dystrophies
Improving muscle function by reducing scarring and restoring dystrophin in Duchenne muscular dystrophy
Improving gene therapy for congenital myasthenic syndrome
Understanding why the effectiveness of molecular patch-based therapies varies in Duchenne muscular dystrophy
Developing a standardised set of measures to support airway clearance of secretions in people with neuromuscular conditions
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