Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 81.71M | 57.80M | 176.23M | 111.30M | 110.70M | 118.19M |
Gross Profit | 79.58M | 57.80M | 154.04M | 99.19M | 101.26M | -62.45M |
EBITDA | -56.86M | -89.09M | -240.71M | -189.17M | -173.90M | -123.87M |
Net Income | -63.31M | -97.94M | -257.83M | -192.28M | -178.30M | -121.12M |
Balance Sheet | ||||||
Total Assets | 97.56M | 101.64M | 165.32M | 562.51M | 721.92M | 938.55M |
Cash, Cash Equivalents and Short-Term Investments | 38.34M | 41.92M | 81.00M | 277.63M | 376.55M | 641.42M |
Total Debt | 23.46M | 30.57M | 38.10M | 43.11M | 48.08M | 42.09M |
Total Liabilities | 77.96M | 78.86M | 82.43M | 267.55M | 346.58M | 441.18M |
Stockholders Equity | 19.60M | 22.77M | 82.89M | 294.96M | 375.34M | 497.37M |
Cash Flow | ||||||
Free Cash Flow | -36.19M | -67.41M | -246.00M | -243.80M | -256.53M | 155.16M |
Operating Cash Flow | -35.90M | -67.14M | -224.84M | -223.63M | -233.25M | 169.88M |
Investing Cash Flow | 1.53M | 37.52M | 153.53M | 59.28M | 248.20M | -271.63M |
Financing Cash Flow | 43.54M | 28.38M | 14.59M | 84.66M | 32.86M | 153.10M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
52 Neutral | 394.17M | -2.27 | -31.51% | ― | ― | ― | |
51 Neutral | $170.44M | ― | -298.41% | ― | 565.52% | 79.44% | |
46 Neutral | 128.17M | -1.42 | ― | ― | -100.00% | 62.82% | |
45 Neutral | 688.71M | -7.12 | ― | ― | ― | 20.37% | |
38 Underperform | 309.88M | -2.17 | ― | ― | ― | -5.57% | |
30 Underperform | 180.54M | -2.60 | ― | ― | ― | -4.60% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On September 4, 2025, Sangamo Therapeutics announced updated clinical data from its Phase 1/2 STAAR study of isaralgagene civaparvovec, a gene therapy for Fabry disease, presented at ICIEM2025 in Kyoto. The study showed promising results, with patients demonstrating stable cardiac function and significant improvements in disease severity and quality of life. The company is preparing a Biologics License Application for accelerated approval, targeting submission in early 2026, contingent on securing additional funding. These developments could enhance Sangamo’s position in the gene therapy market and offer new treatment options for Fabry disease patients.
On June 24, 2025, Sangamo Therapeutics, Inc. announced positive topline results from its Phase 1/2 STAAR study of isaralgagene civaparvovec, a gene therapy for Fabry disease. The study showed significant improvements in kidney function and quality of life measures, with a favorable safety profile. These results support the potential of isaralgagene civaparvovec as a one-time treatment for Fabry disease, paving the way for a Biologics Licensing Application under the Accelerated Approval pathway by early 2026.
On June 12, 2025, Sangamo Therapeutics, Inc. held its annual meeting where stockholders approved significant amendments to the 2018 Equity Incentive Plan. This included increasing the number of shares available for issuance and the number of shares for incentive stock options. The meeting also saw the election of directors, approval of executive compensation, and ratification of Ernst & Young LLP as the company’s independent auditor. These decisions reflect Sangamo’s strategic focus on expanding its equity incentives to attract and retain talent, which could enhance its competitive position in the biotech industry.