| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 6.31M | 8.33M | 15.45M | 2.50M | 0.00 | 0.00 |
| Gross Profit | 6.31M | 8.33M | 15.45M | 2.50M | -492.00K | -9.00K |
| EBITDA | -100.30M | -87.95M | -105.20M | -159.73M | -172.78M | -59.97M |
| Net Income | -99.93M | -89.30M | -111.57M | -166.01M | -175.46M | -43.00M |
Balance Sheet | ||||||
| Total Assets | 316.55M | 160.36M | 172.73M | 126.28M | 213.96M | 258.88M |
| Cash, Cash Equivalents and Short-Term Investments | 297.34M | 139.04M | 143.94M | 87.88M | 149.10M | 251.25M |
| Total Debt | 16.51M | 63.56M | 61.11M | 59.93M | 63.09M | 0.00 |
| Total Liabilities | 97.56M | 88.84M | 97.79M | 125.33M | 118.57M | 7.58M |
| Stockholders Equity | 218.99M | 71.53M | 74.94M | 949.00K | 95.38M | 251.30M |
Cash Flow | ||||||
| Free Cash Flow | -85.16M | -81.60M | -80.39M | -113.26M | -138.60M | -39.81M |
| Operating Cash Flow | -84.68M | -81.22M | -73.02M | -88.39M | -117.04M | -30.73M |
| Investing Cash Flow | -344.00K | -363.00K | -7.35M | -24.93M | -21.55M | -9.08M |
| Financing Cash Flow | 224.68M | 76.68M | 136.39M | 52.10M | 39.08M | 291.06M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
55 Neutral | $1.34B | ― | -81.20% | ― | 16.74% | 59.89% | |
54 Neutral | $1.18B | -3.52 | -46.24% | ― | -76.27% | 22.77% | |
52 Neutral | $1.17B | ― | -64.93% | ― | -36.36% | -945.72% | |
52 Neutral | $894.38M | ― | -23.56% | ― | 22367.80% | -5.15% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $784.06M | ― | -154.81% | ― | 739.42% | 24.90% | |
33 Underperform | $1.06B | ― | -109.12% | ― | ― | 7.58% |
Taysha Gene Therapies’ recent earnings call conveyed a predominantly positive sentiment, driven by notable clinical and regulatory advancements with their TSHA-102 program. The company celebrated significant milestones, such as the Breakthrough Therapy designation and promising clinical data, although these achievements were balanced by increased expenses and net loss.
On November 4, 2025, Taysha Gene Therapies announced amendments to its Sales Agreement, increasing the aggregate offering amount to $212 million, and terminating its agreement with Leerink Partners LLC. The company also reported significant progress in its TSHA-102 program for Rett syndrome, including receiving FDA Breakthrough Therapy designation and finalizing pivotal trial protocols, positioning it to expedite its Biologics License Application submission. Taysha regained full rights to the TSHA-102 program, enhancing its strategic flexibility, and appointed David McNinch as Chief Commercial Officer to strengthen its commercial leadership.
The most recent analyst rating on (TSHA) stock is a Buy with a $13.00 price target. To see the full list of analyst forecasts on Taysha Gene Therapies stock, see the TSHA Stock Forecast page.
The REVEAL Adult Study, officially titled ‘An Open-label, Randomized, Dose-escalation- and Dose-expansion Study of the Safety and Preliminary Efficacy of a Single Intrathecal Administration of TSHA-102, an AAV9-Delivered Gene Therapy, in the Treatment of Adult Females With Rett Syndrome,’ aims to assess the safety and preliminary efficacy of TSHA-102 in adult females with Rett syndrome. This study is significant as it explores a potential gene therapy treatment for a condition with limited therapeutic options.
On October 16, 2025, Taysha Gene Therapies announced it has regained full rights to its lead TSHA-102 program for Rett syndrome after the expiration of a 2022 Option Agreement with Astellas. This development allows Taysha strategic flexibility to advance the program, which has shown promising safety and efficacy data, received FDA Breakthrough Therapy designation, and is poised for a pivotal trial this quarter, highlighting a significant market opportunity given the unmet medical need in Rett syndrome.
The most recent analyst rating on (TSHA) stock is a Buy with a $6.00 price target. To see the full list of analyst forecasts on Taysha Gene Therapies stock, see the TSHA Stock Forecast page.
On October 9, 2025, Taysha Gene Therapies presented new supplemental data from Part A of the REVEAL Phase 1/2 trials for TSHA-102 in Rett syndrome at the 54th CNS Annual Meeting. The analysis showed 100% of patients achieved developmental milestones and additional skill gains, reinforcing TSHA-102’s potential impact on activities of daily living. This suggests a broad and consistent therapeutic effect across core domains of Rett syndrome, which could significantly influence treatment approaches and improve patient and caregiver experiences.
The most recent analyst rating on (TSHA) stock is a Buy with a $14.00 price target. To see the full list of analyst forecasts on Taysha Gene Therapies stock, see the TSHA Stock Forecast page.
On October 2, 2025, Taysha Gene Therapies announced that the FDA granted Breakthrough Therapy designation to TSHA-102 for Rett syndrome, based on positive clinical evidence from their REVEAL Phase 1/2 trials. The company also finalized alignment with the FDA on the pivotal trial protocol and statistical analysis plan, aiming to expedite the Biologics License Application submission, with patient enrollment expected to begin in Q4 2025.
The most recent analyst rating on (TSHA) stock is a Buy with a $13.00 price target. To see the full list of analyst forecasts on Taysha Gene Therapies stock, see the TSHA Stock Forecast page.
Taysha Gene Therapies, Inc. recently held its earnings call, revealing a mixed sentiment. While the company showcased strong progress in clinical trials and regulatory alignment, indicating a positive trajectory, it also faced financial challenges due to increased expenses and net loss.
Taysha Gene Therapies, Inc. is a clinical-stage biotechnology company specializing in adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system, with a focus on developing transformative medicines for conditions like Rett syndrome.