| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 282.08M | 179.28M | 116.88M | 120.24M | 149.24M | 108.62M |
| Gross Profit | 262.62M | 160.63M | 109.77M | 118.49M | 148.15M | 107.73M |
| EBITDA | 124.33M | 28.51M | -16.98M | -53.87M | -11.29M | -27.68M |
| Net Income | 113.30M | 17.48M | -25.09M | -58.57M | -17.91M | -29.74M |
Balance Sheet | ||||||
| Total Assets | 242.53M | 163.98M | 117.22M | 134.28M | 167.33M | 110.38M |
| Cash, Cash Equivalents and Short-Term Investments | 137.14M | 77.32M | 56.93M | 58.21M | 124.97M | 57.33M |
| Total Debt | 60.88M | 59.97M | 60.58M | 41.55M | 30.57M | 39.09M |
| Total Liabilities | 124.92M | 160.69M | 145.87M | 147.90M | 136.95M | 76.35M |
| Stockholders Equity | 117.61M | 3.29M | -28.64M | -13.62M | 30.37M | 34.03M |
Cash Flow | ||||||
| Free Cash Flow | 68.14M | 31.07M | -20.74M | -74.21M | 5.25M | -53.45M |
| Operating Cash Flow | 68.18M | 31.47M | -5.74M | -73.76M | 5.88M | -52.19M |
| Investing Cash Flow | -77.92M | 4.13M | -4.30M | 72.78M | -80.04M | 47.47M |
| Financing Cash Flow | 6.64M | -11.64M | 18.37M | 6.55M | 62.67M | 12.57M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
78 Outperform | $754.91M | 6.74 | 220.06% | ― | 79.13% | 2798.12% | |
54 Neutral | $738.59M | -4.18 | -76.88% | ― | 91.30% | 30.69% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $425.18M | -6.17 | -45.92% | ― | 1255.21% | 74.58% | |
47 Neutral | $476.14M | ― | -34.63% | ― | -23.43% | -9.84% | |
44 Neutral | $584.48M | -1.82 | -2888.70% | ― | 33.79% | -26.37% | |
39 Underperform | $477.76M | -3.01 | ― | ― | -80.09% | 60.14% |
On December 7, 2025, Rigel Pharmaceuticals announced updated data from its ongoing Phase 1b study of R289, an oral prodrug, in patients with relapsed or refractory lower-risk myelodysplastic syndrome (MDS). The study, presented at the 67th ASH Annual Meeting, showed that R289 was generally well tolerated and demonstrated preliminary efficacy, with 33% of evaluable transfusion-dependent patients achieving red blood cell transfusion independence. These results underscore the potential of R289 as a treatment option for lower-risk MDS patients, with further clinical trials anticipated in the second half of 2026.