Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
43.26M | 25.38M | 17.50M | 12.41M | 5.48M | Gross Profit |
31.45M | 15.06M | 6.62M | 4.96M | 1.72M | EBIT |
-63.32M | -49.60M | -48.59M | -45.81M | -35.85M | EBITDA |
-48.99M | -49.78M | -47.88M | -45.42M | -35.53M | Net Income Common Stockholders |
-45.31M | -43.27M | -40.49M | -39.41M | -32.55M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
147.33M | 54.03M | 71.14M | 73.54M | 37.45M | Total Assets |
202.63M | 93.82M | 107.50M | 96.19M | 85.97M | Total Debt |
117.00K | 272.00K | 446.00K | 137.00K | 341.00K | Net Debt |
-121.21M | -53.76M | -54.37M | -73.40M | -27.11M | Total Liabilities |
68.61M | 76.77M | 85.43M | 87.67M | 76.91M | Stockholders Equity |
-134.02M | 17.05M | 22.07M | 8.53M | 9.06M |
Cash Flow | Free Cash Flow | |||
-67.85M | -39.40M | -45.90M | 5.47M | -11.29M | Operating Cash Flow |
-67.64M | -39.35M | -45.46M | 6.81M | -10.78M | Investing Cash Flow |
-21.97M | 16.43M | -16.54M | 8.68M | 9.62M | Financing Cash Flow |
142.09M | 25.16M | 43.05M | 30.71M | 15.43M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
68 Neutral | $144.91B | 18.55 | 9.05% | 6.46% | 8.77% | 272.80% | |
67 Neutral | $7.41B | 32.02 | 19.71% | ― | 52.97% | ― | |
59 Neutral | $36.86B | ― | -414.62% | ― | 22.97% | 38.54% | |
49 Neutral | $6.90B | 0.78 | -53.24% | 2.46% | 20.86% | 1.26% | |
48 Neutral | $13.06B | ― | -28.77% | ― | -52.75% | 25.00% | |
47 Neutral | $162.84M | ― | -99.23% | ― | -40.10% | -16.60% | |
47 Neutral | $2.03B | ― | -600.68% | ― | -98.62% | -86.21% |
Silence Therapeutics reported its financial results for the year ending December 31, 2024, highlighting strong clinical execution and pipeline advancements. The company plans to prioritize investment in siRNA programs targeting rare conditions, with a focus on the divesiran program for polycythemia vera (PV) and the zerlasiran program for cardiovascular disease. Silence ended the year with $147 million in cash, and its decision to delay the zerlasiran Phase 3 study until a partner is secured extends its cash runway into 2027. The company received positive regulatory feedback for the zerlasiran study design and anticipates full enrollment in the SANRECO Phase 2 study of divesiran by the end of 2025.
Silence Therapeutics will transition to filing reports as a U.S. domestic issuer starting January 1, 2025, which entails using more detailed and prompt SEC forms compared to those for a foreign private issuer. This change reflects the company’s growth and could impact its transparency and engagement with stakeholders, as it also utilizes multiple channels to disseminate material information broadly.