Drug Profile

Research programme: ataxia targeted gene therapy - Lacerta Therapeutics

Latest Information Update: 30 Jun 2023

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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

22 May 2023 Lacerta Therapeutics has patents pending for 'compositions and methods for treatment of friedreichs ataxia' in USA, Europe, Japan, Canda, Australia
22 May 2023 Early research in Friedreich's ataxia in USA (Parenteral) (Lacerta Therapeutics website, May 2023)

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