Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | EBIT |
-36.20M | -52.36M | -42.59M | -65.45M | -55.78M | -26.86M | EBITDA |
-35.78M | -52.27M | -42.06M | -64.82M | -55.16M | -26.25M | Net Income Common Stockholders |
-35.80M | -51.21M | -41.05M | -65.26M | -54.71M | -25.70M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
1.08M | 9.25M | 46.96M | 79.13M | 122.39M | 97.60M | Total Assets |
2.46M | 12.99M | 51.03M | 82.53M | 126.26M | 100.48M | Total Debt |
0.00 | 1.01M | 1.30M | 574.00K | 1.07M | 1.53M | Net Debt |
-844.83K | -8.24M | -35.67M | -38.54M | -116.32M | -78.31M | Total Liabilities |
1.36M | 15.89M | 13.29M | 8.29M | 7.35M | 6.55M | Stockholders Equity |
1.10M | -2.90M | 37.74M | 74.24M | 118.92M | 93.93M |
Cash Flow | Free Cash Flow | ||||
-37.18M | -44.62M | -32.35M | -43.52M | -33.97M | -21.66M | Operating Cash Flow |
-37.18M | -44.59M | -32.32M | -43.30M | -33.89M | -21.56M | Investing Cash Flow |
1.96M | 9.96M | 30.07M | -35.21M | 12.63M | -17.37M | Financing Cash Flow |
27.46M | 6.91M | 116.00K | 226.00K | 58.81M | 103.45M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
65 Neutral | $568.85M | 131.14 | 0.53% | ― | 13.13% | ― | |
51 Neutral | $108.86M | ― | -669.49% | ― | ― | ― | |
51 Neutral | $5.20B | 3.26 | -40.34% | 2.93% | 17.68% | 1.94% | |
42 Neutral | $72.59M | ― | -184.69% | ― | ― | 0.10% | |
34 Underperform | $108.22M | ― | -138.82% | ― | ― | -18.03% | |
32 Underperform | $8.37M | ― | 391.94% | ― | ― | 79.63% |
Aptose Biosciences has reported its year-end 2024 results and highlighted significant advancements in its tuspetinib-based triple drug therapy for AML. The ongoing TUSCANY clinical trial has shown promising results, achieving complete remissions in difficult-to-treat AML patients. The company has also signed a debt conversion agreement with Hanmi Pharmaceutical and entered a cooperative research agreement with the National Cancer Institute to further develop tuspetinib. These developments are expected to enhance Aptose’s position in the oncology market and provide additional funding for its clinical programs.
Aptose Biosciences has reported promising early results from their TUSCANY trial, involving the TUS+VEN+AZA triplet therapy for newly diagnosed AML patients. The trial, which uses a combination of tuspetinib, venetoclax, and azacitidine, has shown complete remissions in patients with TP53-mutated and FLT3-wildtype AML, demonstrating favorable safety and efficacy. These results indicate a potential new frontline treatment for a diverse group of AML patients, enhancing Aptose’s position in the oncology field and offering hope for stakeholders.