Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 1.00M | 7.60M | 1.90M | Gross Profit |
0.00 | 0.00 | 900.00K | 7.40M | 1.90M | EBIT |
-31.51M | -37.87M | -41.95M | -25.29M | -16.98M | EBITDA |
-31.51M | 529.00K | -31.95M | -19.66M | -16.40M | Net Income Common Stockholders |
-30.88M | -37.34M | -40.65M | -20.70M | -16.76M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
13.99M | 2.53M | 17.13M | 21.36M | 35.30M | Total Assets |
19.43M | 6.22M | 20.94M | 26.27M | 46.05M | Total Debt |
1.00M | 906.00K | 945.00K | 808.00K | 991.00K | Net Debt |
-12.98M | -1.62M | -16.18M | -20.55M | -34.31M | Total Liabilities |
9.97M | 14.20M | 16.09M | 5.93M | 18.09M | Stockholders Equity |
9.46M | -7.98M | 4.85M | 20.35M | 27.96M |
Cash Flow | Free Cash Flow | |||
-35.40M | -36.91M | -28.31M | -26.02M | -10.42M | Operating Cash Flow |
-35.40M | -31.41M | -23.81M | -26.02M | -10.42M | Investing Cash Flow |
0.00 | -5.50M | -4.50M | 0.00 | 0.00 | Financing Cash Flow |
46.76M | 22.32M | 24.08M | 12.07M | 38.44M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
52 Neutral | $117.17M | ― | -23.91% | ― | -13.92% | -2.86% | |
51 Neutral | $5.35B | 3.41 | -40.48% | 2.89% | 17.92% | 2.25% | |
51 Neutral | $133.31M | ― | -4147.88% | ― | ― | 60.51% | |
48 Neutral | $143.25M | ― | -54.21% | ― | -78.55% | -0.92% | |
42 Neutral | $83.87M | ― | -337.30% | ― | 45.30% | 45.67% | |
36 Underperform | $78.68M | ― | -95.69% | ― | ― | 23.55% | |
33 Underperform | $132.26M | ― | -98.10% | ― | -58.64% | -40.05% |
On January 23, 2025, SELLAS Life Sciences Group announced positive interim results from its Phase 3 REGAL trial evaluating galinpepimut-S (GPS) for acute myeloid leukemia (AML). The Independent Data Monitoring Committee (IDMC) recommended the trial continue without modifications, citing GPS’s safety and efficacy in surpassing futility criteria and showing a promising median survival rate for patients. With fewer than 50% of patients deceased after a median follow-up of 13.5 months, these results indicate a potential shift in standard care for AML, pending further data upon reaching 80 events. The company is preparing for regulatory submissions, indicating potential transformative impacts on treatment options available for AML patients.