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Home » Taysha Gene Therapies to End Development of TSHA-120 After FDA Feedback
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Taysha Gene Therapies to End Development of TSHA-120 After FDA Feedback

News RoomBy News RoomSeptember 21, 20230 Views0
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By Ben Glickman

Taysha Gene Therapies will discontinue development of its TSHA-120 program to treat giant axonal neuropathy after receiving feedback from the U.S. Food and Drug Administration.

The Dallas-based gene-therapy developer said that it had received Type C meeting feedback from the FDA. Chief Executive Sean Nolan said that the feedback…

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