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 | ||||
15.74M | 9.25M | 46.96M | 79.13M | 122.39M | 97.60M | Total Assets |
16.87M | 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 |
-15.30M | -8.24M | -35.67M | -38.54M | -116.32M | -78.31M | Total Liabilities |
2.79M | 15.89M | 13.29M | 8.29M | 7.35M | 6.55M | Stockholders Equity |
14.08M | -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 |
---|---|---|---|---|---|---|---|
70 Outperform | C$606.06M | 138.41 | 0.53% | ― | 13.13% | ― | |
51 Neutral | $110.45M | ― | -669.49% | ― | ― | ― | |
49 Neutral | $6.85B | 0.81 | -52.91% | 2.50% | 19.94% | 1.20% | |
47 Neutral | $73.46M | ― | -184.69% | ― | ― | 0.10% | |
35 Underperform | $10.31M | ― | 391.94% | ― | ― | 60.95% | |
31 Underperform | $112.61M | ― | -158.52% | ― | ― | -21.76% |
Aptose Biosciences announced the dosing of the first patients in the TUSCANY Phase 1/2 trial, which explores tuspetinib in combination with venetoclax and azacitidine as a frontline triplet therapy for newly diagnosed acute myeloid leukemia (AML) patients. This triplet therapy aims to address diverse AML populations and improve response rates and survival while minimizing toxicities, potentially expanding its application to a broader range of AML patients.
Aptose Biosciences has partnered with the National Cancer Institute to develop tuspetinib for acute myeloid leukemia and myelodysplastic syndromes as part of the myeloMATCH precision medicine trials. The collaboration aims to enhance treatment options for these blood cancers through targeted drug combinations, offering new hope for patients. This initiative highlights tuspetinib’s potential in treating challenging genetic cases of AML and MDS.
Aptose Biosciences has launched the TUSCANY Phase 1/2 study to test a new triplet therapy for newly diagnosed acute myeloid leukemia (AML) patients. This innovative treatment combines tuspetinib with azacitidine and venetoclax, aiming to offer an effective frontline therapy for AML patients who cannot undergo intensive chemotherapy. The trial is being conducted across several sites in the United States, with potential to impact a broad range of AML cases.
Aptose Biosciences is advancing the development of its promising drug tuspetinib as part of a triplet therapy for acute myeloid leukemia (AML), showing strong clinical activity and a unique safety profile. The company has secured a $10 million loan from Hanmi Pharmaceutical to support the clinical development of tuspetinib, with plans for a new co-development collaboration. Tuspetinib has demonstrated potential to address unmet needs in AML treatment by avoiding common toxicities associated with other therapies.