Compare FTRE & TSHA Stocks: Price Trends, ML Decisions, Charts, Trends, Technical Analysis and more.
Current Price
Current Price
| Metric | FTRE | TSHA |
|---|---|---|
| Founded | 1996 | 2019 |
| Country | United States | United States |
| Employees | N/A | N/A |
| Industry | Medical Specialities | Biotechnology: Pharmaceutical Preparations |
| Sector | Health Care | Health Care |
| Exchange | Nasdaq | Nasdaq |
| Market Cap | 1.9B | 1.7B |
| IPO Year | 2023 | 2020 |
| Metric | FTRE | TSHA |
|---|---|---|
| Price | $21.51 | $4.33 |
| Analyst Decision | Buy | Strong Buy |
| Analyst Count | 13 | 13 |
| Target Price | ★ $20.67 | $13.00 |
| AVG Volume (30 Days) | 1.3M | ★ 3.1M |
| Earning Date | 10-29-2026 | 11-03-2026 |
| Dividend Yield | N/A | N/A |
| EPS Growth | N/A | ★ 5.56 |
| EPS | N/A | ★ N/A |
| Revenue | ★ $2,723,400,000.00 | $9,773,000.00 |
| Revenue This Year | N/A | N/A |
| Revenue Next Year | $3.05 | $1,023.00 |
| P/E Ratio | ★ N/A | N/A |
| Revenue Growth | 1.00 | ★ 17.28 |
| 52 Week Low | $8.55 | $3.69 |
| 52 Week High | $21.39 | $7.30 |
| Indicator | FTRE | TSHA |
|---|---|---|
| Relative Strength Index (RSI) | 65.64 | 28.58 |
| Support Level | $15.94 | N/A |
| Resistance Level | N/A | $4.72 |
| Average True Range (ATR) | 1.08 | 0.26 |
| MACD | 0.14 | -0.03 |
| Stochastic Oscillator | 55.38 | 8.75 |
Fortrea is a global, late-stage contract research organization that provides comprehensive phase 1 through phase 4 clinical trial management, clinical pharmacology, and patient access solutions. The company works with emerging and large biopharma, medical device, and diagnostic companies to run their clinical trials as a functional-service provider, full-service provider, and offers hybrid trials. In 2023, Fortrea was formed as an independent, publicly traded company after Labcorp spun off its clinical development business, which it acquired via its purchase of Covance in 2015 for $6.1 billion.
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.