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TAYSHA GENE THERAPIES INC (TSHA)

Health Care · Gene therapy / AAV-based therapeutics for rare neurological disorders · NASDAQ

Clinical-stage gene therapy company developing an AAV9-based treatment (TSHA-102) for Rett syndrome with early-stage clinical data showing functional gains in treated patients.

What TAYSHA GENE THERAPIES INC does

Taysha Gene Therapies is a clinical-stage biotechnology company developing AAV-based gene therapies for severe monogenic diseases of the central nervous system. The company's lead program, TSHA-102, is in development for the treatment of Rett syndrome, a rare neurodevelopmental disorder caused by MECP2 loss-of-function mutations. TSHA-102 is currently being evaluated in Phase 1/2 clinical trials (REVEAL and ASPIRE) with the goal of demonstrating safety and efficacy for approval across a broad patient population aged 2 years and older.

Themes: ["rare genetic disease / neurogenetic disorders","gene therapy / AAV-based therapeutics","CNS disorders","Rett syndrome"]

Fundamentals

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Key risks (from latest filing)

["Clinical failure: TSHA-102 may not meet efficacy endpoints in pivotal trials (REVEAL Part B, ASPIRE), jeopardizing regulatory approval for Rett syndrome.","Manufacturing and supply: As a cell and gene therapy manufacturer, the company faces operational complexity, regulatory scrutiny, and potential supply chain constraints that could delay or limit treatment availability.","Capital requirements: The company is unprofitable with declining cash reserves ($276.6M as of Q1 2026 vs. $319.8M at year-end 2025) and will require additional funding to complete clinical development and commercialization, which may involve dilutive equity financing or unfavorable debt terms."]

See TSHA's biggest risks from its latest 10-Q →

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Fundamentals: Finnhub, as of 2026-07-10. Filings: SEC EDGAR. Prices are delayed daily-close data.

Last updated 2026-07-09.

Informational only — NOT financial advice. All figures are delayed daily-close data from SEC EDGAR & Finnhub, shown with their as-of date.