Taysha outlines 2026 BLA submission path for TSHA-102 as pivotal trial enrollment advances

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Taysha Gene Therapies is advancing its pivotal clinical trial for TSHA-102, a gene therapy for Rett syndrome, with patient enrollment progressing. The company has outlined a plan for a Biologics License Application (BLA) submission in 2026 to the FDA, following discussions and encouraging interim data. This strategy aims to bring the potential treatment to patients sooner by leveraging existing data.

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