Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
956.22K | 583.23K | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
939.77K | 576.18K | -186.44K | -271.68K | -229.61K | -170.25K | EBIT |
-14.77M | -15.47M | 38.18M | -38.04M | -52.15M | -31.04M | EBITDA |
-14.52M | -14.28M | -112.48M | -36.86M | -53.25M | -27.89M | Net Income Common Stockholders |
-13.51M | -14.29M | -224.88M | -36.54M | -53.92M | -26.41M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
65.68M | 21.61M | 28.79M | 53.08M | 89.02M | 130.09M | Total Assets |
66.02M | 22.65M | 30.16M | 56.82M | 92.81M | 133.61M | Total Debt |
0.00 | 0.00 | 0.00 | 190.47K | 335.16K | 544.95K | Net Debt |
-65.68M | -21.61M | -28.79M | -52.89M | -88.68M | -129.54M | Total Liabilities |
117.46M | 5.70M | 4.51M | 7.32M | 15.41M | 9.36M | Stockholders Equity |
-51.44M | 18.26M | 25.64M | 49.51M | 77.40M | 124.24M |
Cash Flow | Free Cash Flow | ||||
-6.41M | -12.27M | -25.01M | -37.69M | -41.83M | -26.74M | Operating Cash Flow |
-13.81M | -12.18M | -25.01M | -37.69M | -41.80M | -26.71M | Investing Cash Flow |
― | -93.09K | 0.00 | 0.00 | -25.71K | -30.90K | Financing Cash Flow |
14.58M | 5.14M | 682.97K | 1.75M | 150.95K | 92.58M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
59 Neutral | $3.88B | ― | -31.41% | ― | 49.59% | 24.92% | |
53 Neutral | $932.65M | ― | -50.50% | ― | ― | 4.28% | |
51 Neutral | $13.32M | ― | -60.22% | ― | 130.31% | 86.90% | |
49 Neutral | $6.84B | 0.05 | -53.14% | 2.48% | 24.49% | -3.26% | |
45 Neutral | $591.93M | ― | -42.91% | ― | ― | 2.90% | |
45 Neutral | $6.91M | ― | -30.36% | ― | ― | 86.52% | |
39 Underperform | $65.44M | ― | -29.23% | ― | ― | 21.33% |
Aprea Therapeutics has announced promising preliminary safety results for its WEE1 inhibitor, APR-1051, showcased at an international oncology conference. The Phase 1 trial indicates APR-1051 is safe and well-tolerated without serious side effects, presenting potential as a treatment for advanced solid tumors. With ongoing trials in the U.S., the company is optimistic about further exploring APR-1051’s therapeutic potential, aiming for more efficacy data in 2025.