Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
767.39K | 1.50M | 583.23K | 0.00 | 0.00 | 0.00 |
Gross Profit | |||||
756.66K | 1.48M | 576.18K | -186.44K | -271.68K | -229.61K |
EBIT | |||||
-15.26M | -14.32M | -15.47M | 38.18M | -38.04M | -52.15M |
EBITDA | |||||
-15.24M | -12.94M | -14.28M | -112.48M | -36.86M | -53.25M |
Net Income Common Stockholders | |||||
-14.08M | -12.96M | -14.29M | -224.88M | -36.54M | -53.92M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
19.28M | 22.85M | 21.61M | 28.79M | 53.08M | 89.02M |
Total Assets | |||||
20.22M | 23.98M | 22.65M | 30.16M | 56.82M | 92.81M |
Total Debt | |||||
0.00 | 0.00 | 0.00 | 0.00 | 190.47K | 335.16K |
Net Debt | |||||
-19.28M | -22.85M | -21.61M | -28.79M | -52.89M | -88.68M |
Total Liabilities | |||||
4.67M | 4.67M | 5.70M | 4.51M | 7.32M | 15.41M |
Stockholders Equity | |||||
15.55M | 19.31M | 18.26M | 25.64M | 49.51M | 77.40M |
Cash Flow | Free Cash Flow | ||||
-9.61M | -13.57M | -12.27M | -25.01M | -37.69M | -41.83M |
Operating Cash Flow | |||||
-13.15M | -13.56M | -12.18M | -25.01M | -37.69M | -41.80M |
Investing Cash Flow | |||||
0.00 | -15.48K | -93.09K | 0.00 | 0.00 | -25.71K |
Financing Cash Flow | |||||
-30.82K | 14.82M | 5.14M | 682.97K | 1.75M | 150.95K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
56 Neutral | $9.16M | 4.67 | -41.13% | ― | ― | ― | |
54 Neutral | $5.34B | 3.27 | -45.10% | 3.30% | 16.80% | 0.02% | |
51 Neutral | $3.37M | ― | -205.75% | ― | 2552.29% | 60.70% | |
49 Neutral | $8.89M | ― | -451.34% | ― | ― | -57.84% | |
48 Neutral | $18.87M | ― | -362.79% | ― | 32.45% | 39.31% | |
40 Underperform | $9.79M | ― | -59.80% | ― | 157.63% | 40.52% | |
39 Underperform | $7.21M | ― | -285.79% | ― | ― | 23.65% |
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.