| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 678.55K | 1.50M | 583.23K | 0.00 | 0.00 | 0.00 |
| Gross Profit | 819.30K | 1.48M | 576.18K | -186.44K | -271.68K | -229.61K |
| EBITDA | -14.79M | -12.94M | -14.28M | -112.48M | -36.86M | -53.25M |
| Net Income | -13.85M | -12.96M | -14.29M | -224.88M | -36.54M | -53.92M |
Balance Sheet | ||||||
| Total Assets | 17.31M | 23.98M | 22.65M | 30.16M | 56.82M | 92.81M |
| Cash, Cash Equivalents and Short-Term Investments | 16.53M | 22.85M | 21.61M | 28.79M | 53.08M | 89.02M |
| Total Debt | 0.00 | 0.00 | 0.00 | 0.00 | 190.47K | 335.16K |
| Total Liabilities | 3.90M | 4.67M | 4.39M | 4.51M | 7.32M | 15.41M |
| Stockholders Equity | 14.14M | 19.31M | 18.26M | 25.64M | 49.51M | 77.40M |
Cash Flow | ||||||
| Free Cash Flow | -12.74M | -13.57M | -12.27M | -25.01M | -37.69M | -41.83M |
| Operating Cash Flow | -12.74M | -13.56M | -12.18M | -25.01M | -37.69M | -41.80M |
| Investing Cash Flow | -209.00 | -15.48K | -93.09K | 0.00 | 0.00 | -25.71K |
| Financing Cash Flow | 573.98K | 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 |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $8.91M | -0.41 | -67.73% | ― | -2.06% | 64.86% | |
40 Underperform | $9.15M | ― | -67.54% | ― | -34.07% | 23.79% | |
34 Underperform | $9.76M | ― | -165.56% | ― | ― | 58.67% | |
28 Underperform | $7.67M | >-0.01 | -563.25% | ― | ― | 80.34% | |
25 Underperform | $7.12M | -0.03 | -244.31% | ― | ― | -146.64% |
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.