| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 486.39K | 1.50M | 583.23K | 0.00 | 0.00 | 0.00 |
| Gross Profit | -6.27M | -7.86M | 576.18K | -16.40M | -271.68K | -229.61K |
| EBITDA | -13.65M | -14.30M | -14.28M | -37.37M | -36.86M | -53.25M |
| Net Income | -13.04M | -12.96M | -14.29M | -112.66M | -36.54M | -53.92M |
Balance Sheet | ||||||
| Total Assets | 14.32M | 23.98M | 22.65M | 30.16M | 56.82M | 92.81M |
| Cash, Cash Equivalents and Short-Term Investments | 13.72M | 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 | 2.68M | 4.67M | 4.39M | 4.51M | 7.32M | 15.41M |
| Stockholders Equity | 11.64M | 19.31M | 18.26M | 25.64M | 49.51M | 77.40M |
Cash Flow | ||||||
| Free Cash Flow | -13.44M | -13.57M | -12.27M | -25.01M | -37.69M | -41.83M |
| Operating Cash Flow | -13.44M | -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 | 933.07K | 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% | |
45 Neutral | $8.34M | -0.36 | -70.67% | ― | 6.29% | 7.42% | |
40 Underperform | $7.64M | -0.57 | -74.72% | ― | -62.75% | 23.87% | |
34 Underperform | $7.49M | -0.16 | -189.72% | ― | ― | 70.57% | |
28 Underperform | $6.93M | >-0.01 | -563.25% | ― | ― | 80.34% | |
25 Underperform | $5.80M | -0.02 | -655.85% | ― | ― | -389.35% |
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.