Duchenne Muscular Dystrophy

DMD is a fatal genetic disease that occurs in approximately 1 in 5,000 males with one third of cases arising in boys with no familial history of the disease.

Our utrophin modulation programme is a potential disease-modifying approach to treat all patients with DMD.

Duchenne Muscular Dystrophy image boy

C. difficile Infection

Infection caused by the bacterium C. difficile is a major healthcare threat in hospitals, long-term care homes, and increasingly in the wider community.

We are developing ridinilazole (SMT19969), a highly selective antibiotic that has the potential to treat CDI and reduce disease recurrence, the primary clinical issue.

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Publications

We regularly publish data on our drug programmes in peer-reviewed journals and gives presentations at leading international conferences. This section provides access to this information.

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