Drug Profile

DYST 201

Alternative Names: DYST-201; Huntington’s disease gene therapy - Dystrogen Therapeutics

Latest Information Update: 03 Dec 2019

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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

29 Nov 2019 Discontinued - Preclinical for Huntington's disease in USA (Intrathecal) (Dystrogen Therapeutics pipeline, November 2019)
05 Apr 2019 Preclinical trials in Huntington's disease in USA (Intrathecal) before April 2019 (Dystrogen Therapeutics pipeline, April 2019)

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