Drug Profile

Research programme: gene therapies - Myosana Therapeutics

Alternative Names: Non-viral Duchenne muscular dystrophy gene therapy - Myosana Therapeutics

Latest Information Update: 28 May 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

No development reported Duchenne muscular dystrophy; Neuromuscular disorders

28 May 2024 No recent reports of development identified for research development in Duchenne muscular dystrophy in USA (Parenteral)
28 May 2024 No recent reports of development identified for research development in Neuromuscular-disorders in USA (Parenteral)
22 Apr 2020 Early research in Duchenne muscular dystrophy in USA (Parenteral)

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