Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 38.90M | 32.31M | 78.12M | 19.71M | 25.54M | 90.73M |
Gross Profit | 35.92M | 26.50M | 72.06M | 13.38M | 20.49M | -67.26M |
EBITDA | -225.89M | -233.11M | -163.12M | -219.61M | -188.09M | -130.88M |
Net Income | -236.86M | -237.09M | -153.22M | -220.43M | -192.50M | -115.98M |
Balance Sheet | ||||||
Total Assets | 210.58M | 341.59M | 499.15M | 514.32M | 677.48M | 572.60M |
Cash, Cash Equivalents and Short-Term Investments | 178.50M | 269.91M | 323.11M | 344.27M | 499.85M | 402.11M |
Total Debt | 77.81M | 35.03M | 36.54M | 43.95M | 26.38M | 26.14M |
Total Liabilities | 191.39M | 207.31M | 150.06M | 153.64M | 123.84M | 179.02M |
Stockholders Equity | 19.19M | 134.27M | 349.10M | 360.68M | 553.64M | 393.59M |
Cash Flow | ||||||
Free Cash Flow | -204.94M | -219.11M | -136.90M | -181.47M | -171.78M | -187.00M |
Operating Cash Flow | -201.36M | -210.28M | -132.18M | -177.35M | -163.80M | -179.84M |
Investing Cash Flow | 213.97M | 162.15M | -3.73M | 114.07M | -54.47M | -140.52M |
Financing Cash Flow | 61.49M | 56.03M | 118.04M | 1.28M | 282.11M | 224.12M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
64 Neutral | $227.17M | ― | -48.36% | ― | 334.10% | ― | |
51 Neutral | $7.93B | -0.35 | -43.30% | 2.25% | 22.54% | -2.22% | |
51 Neutral | $241.89M | ― | -188.58% | ― | -41.97% | -20.86% | |
39 Underperform | $139.92M | ― | -26.94% | ― | ― | 26.33% | |
39 Underperform | $268.24M | ― | -77.83% | ― | ― | 43.16% | |
39 Underperform | $346.46M | ― | -29.24% | ― | ― | -125.92% | |
33 Underperform | $262.35M | ― | -89.37% | ― | ― | 9.84% |
On September 2, 2025, Editas Medicine announced the nomination of EDIT-401 as its lead in vivo development candidate. EDIT-401 is designed to reduce LDL cholesterol levels by editing the LDLR gene, showing promising preclinical results with a significant reduction in LDL-C levels and increased LDLR protein expression. The company plans to focus on advancing EDIT-401 to human proof-of-concept and aims to submit an IND or CTA by mid-2026. Additionally, Editas confirmed its financial stability, projecting its cash runway to extend into the second quarter of 2027.
On June 12, 2025, Editas Medicine announced new in vivo data at the European Hematology Association 2025 Congress, demonstrating significant advancements in gene editing for sickle cell disease and beta thalassemia. The study showed that a single dose of their proprietary targeted lipid nanoparticle (tLNP) in non-human primates achieved a 58% mean on-target editing level in the HBG1/2 promoter region of hematopoietic stem cells, surpassing the therapeutic threshold. This development supports the potential of Editas’ approach to provide a novel treatment for these conditions, with favorable biodistribution and minimal liver targeting, enhancing the company’s position in the gene editing industry.