Taysha Gene Therapies, Inc., a clinical-stage biotechnology company, focuses on developing and commercializing adeno-associated virus-based gene therapies for the treatment of severe monogenic diseases of the central nervous system. The company primarily develops TSHA-120 for the treatment of giant axonal neuropathy; TSHA-102 for the treatment of Rett syndrome; TSHA-121 for the treatment of CLN7 disease; TSHA-118 for the treatment of CLN1 disease; TSHA-105 for the treatment of SLC13A5 deficiency; TSHA-113 for the treatment of tauopathies; TSHA-106 for the treatment of angelman syndrome; and TSHA-114 for the treatment of fragile X syndrome. The company has research, collaboration, and license agreement with The University of Texas Southwestern Medical Center. Taysha Gene Therapies, Inc. was incorporated in 2019 and is headquartered in Dallas, Texas.
Market Momentum | Analysts set price targets ranging from $5 to $7, reflecting optimism in Taysha's potential to capture significant market share in rare disease treatments |
Financial Fortitude | $312.8M cash balance supports operations into 2028, with analysts projecting potential revenues exceeding $2B for Rett syndrome treatment |
Regulatory Fast Track | FDA alignment on pivotal trial design and RMAT designation accelerate Taysha's path to potential approval, bypassing traditional development stages |
Promising Pipeline | Taysha's TSHA-102 for Rett syndrome shows 100% response rate in trials, positioning the company as a frontrunner in gene therapy for CNS disorders |
Metrics to compare | TSHA | Sector Sector - Average of metrics from a broad group of related Healthcare sector companies | Relationship RelationshipTSHAPeersSector | |
|---|---|---|---|---|
P/E Ratio | −13.6x | −8.8x | −0.5x | |
PEG Ratio | −2.76 | −0.27 | 0.00 | |
Price / Book | 6.0x | 3.2x | 2.6x | |
Price / LTM Sales | 151.5x | 18.4x | 3.2x | |
Upside (Analyst Target) | 144.2% | 61.6% | 47.6% | |
Fair Value Upside | Unlock | −7.8% | 6.1% | Unlock |