Lexeo Therapeutics granted FDA fast track designation and orphan drug designation for LX2020, an AAV based gene therapy candidate for PKP2 arrhythmogenic cardiomyopathy

Lexeo Therapeutics

18 December 2023 - Lexeo Therapeutics today announced the US FDA has granted fast track designation and orphan drug designation to LX2020, the company’s AAVrh10 based gene therapy candidate designed to intravenously deliver a functional PKP2 gene to cardiac muscle for the treatment of arrhythmogenic cardiomyopathy caused by mutations in the PKP2 gene (PKP2-ACM).

LX2020 is an AAVrh10 based gene therapy candidate designed to intravenously deliver a functional PKP2 gene to cardiac muscle for the treatment of PKP2-ACM.

Read Lexeo Therapeutics press release

Michael Wonder

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Michael Wonder

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US , Gene therapy , Fast track