| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 61.52M | 210.78M | 129.01M | 0.00 | 0.00 | 0.00 |
| Gross Profit | 23.16M | 210.78M | 129.01M | 0.00 | 0.00 | -326.00K |
| EBITDA | -113.78M | 47.01M | -321.00K | -95.35M | -50.01M | -26.20M |
| Net Income | -103.45M | 65.63M | -6.68M | -94.62M | -51.16M | -26.52M |
Balance Sheet | ||||||
| Total Assets | 412.90M | 526.32M | 469.19M | 252.06M | 305.83M | 43.53M |
| Cash, Cash Equivalents and Short-Term Investments | 326.84M | 420.00M | 351.97M | 188.71M | 291.06M | 39.05M |
| Total Debt | 52.40M | 59.21M | 68.23M | 25.94M | 0.00 | 0.00 |
| Total Liabilities | 72.18M | 97.64M | 226.83M | 39.50M | 7.12M | 85.02M |
| Stockholders Equity | 340.72M | 428.68M | 242.36M | 212.55M | 298.72M | -41.49M |
Cash Flow | ||||||
| Free Cash Flow | -129.80M | -44.72M | 134.19M | -96.67M | -55.44M | -27.89M |
| Operating Cash Flow | -127.91M | -41.56M | 139.80M | -93.79M | -50.86M | -25.57M |
| Investing Cash Flow | 141.05M | -27.80M | -138.40M | -148.65M | -4.58M | -2.32M |
| Financing Cash Flow | 2.10M | 102.96M | 21.04M | 479.00K | 307.46M | 50.09M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
63 Neutral | $994.46M | -9.24 | -45.35% | ― | ― | 36.65% | |
59 Neutral | $158.96M | 7.36 | 19.23% | ― | ― | ― | |
52 Neutral | $404.36M | -4.32 | -27.11% | ― | -71.42% | -248.91% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $197.48M | -3.50 | -39.78% | ― | ― | -38.23% | |
44 Neutral | $225.81M | -1.33 | -59.98% | ― | -10.57% | 1.98% |
On January 8, 2026, Entrada Therapeutics reported significant 2025–early 2026 progress across its RNA-based pipeline for neuromuscular and ocular diseases, including completion of Cohort 1 dosing in the global Phase 1/2 MAD ELEVATE-44-201 study of ENTR-601-44 in Duchenne muscular dystrophy (DMD), transition to the open-label Phase 2 portion, and receipt of Rare Pediatric Disease Designation from the U.S. FDA in December 2025. The company has initiated dosing in the Phase 1/2 MAD ELEVATE-45-201 trial of ENTR-601-45, secured U.K. authorization to start a Phase 1/2 MAD study of ENTR-601-50 in DMD patients amenable to exon 50 skipping, plans regulatory filings for ENTR-601-51 in 2026, and continues to support Vertex’s ongoing global Phase 1/2 trial of VX-670 in myotonic dystrophy type 1, targeting completion of the MAD portion’s enrollment and dosing in the first half of 2026. Entrada also expanded into ophthalmology by selecting ENTR-801 in December 2025 as its first ocular clinical candidate for Usher syndrome type 2A, supported by robust preclinical data, and indicated that around 15,000 US and European patients may be addressable by exon 13 skipping; coupled with a reported cash runway into the third quarter of 2027 and a high-profile investor presentation scheduled for January 14, 2026 at the J.P. Morgan Healthcare Conference, these developments underscore the company’s intent to solidify its position as a leading player in RNA-based therapies for high-unmet-need genetic diseases.
The most recent analyst rating on (TRDA) stock is a Hold with a $7.50 price target. To see the full list of analyst forecasts on Entrada Therapeutics Inc stock, see the TRDA Stock Forecast page.