Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
1.43M | 1.66M | 8.23M | 1.33M | 29.57M | 7.89M | Gross Profit |
1.28M | 1.51M | 7.87M | 1.12M | 29.40M | 7.89M | EBIT |
-25.88M | -28.88M | -24.84M | -30.28M | -627.00K | -17.93M | EBITDA |
-20.22M | -24.35M | -23.06M | -29.46M | -449.00K | -17.93M | Net Income Common Stockholders |
-30.81M | -34.35M | -32.48M | -34.07M | 376.00K | -18.03M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
13.63M | 20.02M | 28.92M | 48.26M | 30.44M | 17.29M | Total Assets |
19.67M | 25.13M | 34.02M | 51.30M | 42.90M | 19.32M | Total Debt |
619.00K | 703.00K | 43.00M | 1.28M | 675.00K | 1.98M | Net Debt |
-13.01M | -19.32M | 14.08M | -46.97M | -29.76M | -15.31M | Total Liabilities |
65.58M | 63.98M | 49.93M | 40.70M | 4.93M | 10.56M | Stockholders Equity |
-45.91M | -38.85M | -15.91M | 10.61M | 37.98M | 8.76M |
Cash Flow | Free Cash Flow | ||||
-23.60M | -25.68M | -19.91M | -13.61M | -10.73M | -13.18M | Operating Cash Flow |
-22.68M | -24.70M | -18.14M | -13.37M | -10.73M | -13.12M | Investing Cash Flow |
-590.00K | -638.00K | -1.78M | -246.00K | 0.00 | -55.00K | Financing Cash Flow |
1.54M | 16.44M | 414.00K | 31.33M | 23.78M | 7.87M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
52 Neutral | $5.19B | 3.04 | -44.64% | 2.82% | 16.45% | -0.53% | |
44 Neutral | $93.04M | ― | -122.69% | ― | ― | 20.91% | |
43 Neutral | $68.30M | ― | 91.63% | ― | -55.47% | 24.92% | |
41 Neutral | $46.17M | ― | -127.99% | ― | ― | 37.54% | |
37 Underperform | $257.60M | ― | -141.69% | ― | ― | -17.06% | |
36 Underperform | $83.38M | ― | -55.14% | ― | -99.43% | -69.40% | |
35 Underperform | $74.06M | ― | -101.34% | ― | ― | 21.40% |
On March 27, 2025, Clearside Biomedical announced its financial results for the fourth quarter and full year 2024, alongside a corporate update. The company reported a decrease in license and other revenue, attributing it to prior year milestone payments, and a net loss increase due to reduced revenue. Clearside highlighted its successful End-of-Phase 2 meeting with the FDA for CLS-AX in wet AMD, and its Asia-Pacific partner’s regulatory progress for ARCATUS® in China. The company also noted multiple collaborations and advancements in its suprachoroidal delivery platform, including Phase 3 plans for diabetic retinopathy and ocular oncology trials, positioning itself for potential pipeline expansion and strategic partnerships.