Drug Profile

Research programme: CNS targeted gene therapies - Lacerta Therapeutics

Latest Information Update: 28 Jun 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 Cardiomyopathies; CNS disorders; Glycogen storage disease type II; Multiple sclerosis

28 Jun 2024 No recent reports of development identified for preclinical development in Cardiomyopathies in USA (Parenteral)
28 Jun 2024 No recent reports of development identified for research development in Multiple-sclerosis in USA (Parenteral)
28 Sep 2022 No recent reports of development identified for research development in CNS-disorders in USA (Parenteral)

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