Drug Profile

Research programme: neuromuscular disorders therapeutics - Genea Biocells

Latest Information Update: 28 Dec 2022

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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 Yes

No development reported Muscular dystrophies; Myotonic dystrophy; Spinal muscular atrophy

28 Dec 2022 No recent reports of development identified for research development in Muscular-dystrophies in USA
28 Dec 2022 No recent reports of development identified for research development in Myotonic dystrophy in USA
28 Dec 2022 No recent reports of development identified for research development in Spinal-muscular-atrophy in USA

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