Drug Profile

Research programme: neuromuscular gene therapies - Locanabio

Latest Information Update: 28 Oct 2024

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At a glance

Originator Locanabio
Class Gene therapies
Mechanism of Action RNA modulators

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
Available For Licensing Yes

Highest Development Phases

No development reported Inborn genetic disorders; Myotonic dystrophy

Most Recent Events

28 Oct 2024 No recent reports of development identified for preclinical development in Myotonic dystrophy in USA (IM, Injection)
28 Oct 2024 No recent reports of development identified for preclinical development in Myotonic dystrophy in USA (Parenteral, Injection)
28 Jun 2023 No recent reports of development identified for research development in Inborn genetic disorders in USA (Parenteral, Injection)

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