Drug Profile

Research programme: muscular dystrophy therapeutics - Healx/Muscular Dystrophy UK

Latest Information Update: 28 Aug 2024

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At a glance

Orphan Drug Status

Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

No
New Molecular Entity No

28 Aug 2024 No recent reports of development identified for research development in Facioscapulohumeral-muscular-dystrophy in United Kingdom
15 Jul 2020 Healx signs collaborative research agreement with Muscular Dystrophy UK for development of therapeutics in Facioscapulohumeral muscular dystrophy
15 Jul 2020 Early research in Facioscapulohumeral muscular dystrophy in United Kingdom (unspecified route)

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