Drug Profile

Research programme: repeat expansion disorders therapeutics - Triplet Therapeutics

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 Yes
Available For Licensing Yes

No development reported Huntington's disease; Myotonic dystrophy; Spinocerebellar degeneration

28 Aug 2024 No recent reports of development identified for preclinical development in Huntington's-disease in USA (Parenteral)
28 Jan 2024 No recent reports of development identified for research development in Myotonic dystrophy in USA (Parenteral)
28 Jan 2024 No recent reports of development identified for research development in Spinocerebellar-degeneration in USA (Parenteral)

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