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Taysha Gene Therapies/$TSHA

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About Taysha Gene Therapies

Taysha Gene Therapies Inc is a clinical-stage biotechnology company focused on advancing AAV-based gene therapies for the treatment of severe monogenic diseases of the central nervous system, or CNS. The company's clinical program TSHA-102 is in development for the treatment of Rett syndrome, a rare neurodevelopmental disorder with no approved disease-modifying therapies that address the genetic root cause of the disease. The Company views its operations and manages its business as a single operating segment, the gene therapy segment, which is the business of developing AAV-based gene therapies for the treatment of rare monogenic diseases of the central nervous system.
Ticker
$TSHA
Sector
Health
Primary listing
NASDAQ
Employees
99

TSHA Metrics

BasicAdvanced
$1.3B
-
-$0.41
1.19
-

What the Analysts think about TSHA

Analyst ratings (Buy, Hold, Sell) for Taysha Gene Therapies stock.
Analyst projections of the future price of Taysha Gene Therapies stock.

Bulls say / Bears say

In the 12-patient Part A cohort, all participants had gained or regained at least one developmental milestone by 12 months, and milestone gains continued to increase with longer follow-up. Taysha also reported no treatment-related serious adverse events or dose-limiting toxicities across 29 treated patients as of June. (GlobeNewswire)
Dosing is complete in the 17-patient REVEAL pivotal trial, and Taysha says the FDA has aligned on a pathway that could allow a six-month interim analysis to support a BLA. Interim results and FDA feedback are expected in the first half of 2027, creating a clear regulatory catalyst. (GlobeNewswire)
Taysha reported $455.4 million in cash at the end of June and expects its runway to extend into the second half of 2028. It has also secured Catalent as its primary commercial manufacturing partner, helping prepare supply if TSHA-102 is approved. (StockTitan, Investing News Network)
The efficacy evidence is still based on a small early-stage cohort: Part A had 12 patients, while the pivotal study is a 17-patient, single-arm trial. Without a concurrent control group, results may be sensitive to patient variation and the choice of milestone endpoint. (GlobeNewswire, BioSpace)
The regulatory timeline remains dependent on future milestones: pivotal interim results and FDA feedback are not expected until the first half of 2027, while manufacturing qualification was still targeted for completion in the fourth quarter of 2026. Delays or unfavourable feedback could push back a filing and any launch. (GlobeNewswire, Last10K)
The company funded much of its longer runway through a $230 million follow-on offering that included common shares and pre-funded warrants, diluting existing holders. Meanwhile, its second-quarter net loss widened to $46.6 million from $26.9 million a year earlier as research and development costs rose. (StockTitan)
Data summarised monthly by Lightyear AI. Last updated on 5 Oct 2026.

TSHA Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

TSHA Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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