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TSHA-121 is a gene therapy investigational drug developed using adeno-associated virus (AAV) vector technology, indicated for the treatment of neurological disorders[5]. Specific disease indications, mechanism of action, and agent composition have not been disclosed in publicly available sources[5][7]. TSHA-121 was initially developed by The University of Texas Southwestern Medical Center and its most advanced R&D status is preclinical or early-phase clinical investigation[5].
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