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Research

Every day Muscular Dystrophy UK is working towards a future with effective treatments and ultimately cures for all muscle-wasting conditions and where there are no limits in life for people who are affected. We believe in this vision this as passionately now as we did when we were established in 1959.
A teenage boy assists a researcher wearing a lab coat and gloves with some testing in a laboratory.
A researcher wearing safety goggles and a lab coat conducts tests in a laboratory.
Our research
Find out about our pioneering research into muscle-wasting conditions.
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A seated researcher in a green lab coat in discussion with three colleagues wearing white lab coats.
Understanding research
Research can be complex and at times confusing. So we’ve brought together some useful resources to help you understand how research works.
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For researchers
Funding opportunities and resources for researchers
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researcher
Get involved in research
From lay panels to clinical trials, find out how to get involved in research into muscle-wasting conditions
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Research news

News-Update
US FDA advisory committee votes on Sarepta SRP-9001 gene therapy to treat Duchenne muscular dystrophy ahead of a FDA’s final decision
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News-Update
UK sites are now recruiting people with FSHD to take part in a clinical trial
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Breaking news
Breaking News
NICE publishes final guidance recommending access to Duchenne muscular dystrophy treatment Translarna
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