Atsena Therapeutics granted US FDA fast track designation for ATSN-201 gene therapy to treat X-linked retinoschisis

Atsena Therapeutics

12 March 2025 - Marks third FDA designation for ATSN-201, which has also received rare paediatric disease designation and orphan drug designation.

Atsena Therapeutics today announced that the US FDA has granted fast track designation for ATSN-201 for the treatment of X-linked retinoschisis.

Read Atsena Therapeutics press release

Michael Wonder

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Michael Wonder