| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 41.28M | 37.87M | 39.55M | 42.01M | 35.99M | 37.44M |
| Gross Profit | 34.88M | 31.28M | 33.49M | 32.89M | 27.17M | 28.79M |
| EBITDA | 2.68M | 182.42K | 2.49M | 332.92K | -857.83K | -1.56M |
| Net Income | -3.33M | -6.48M | -6.28M | -5.57M | -3.51M | -3.34M |
Balance Sheet | ||||||
| Total Assets | 65.90M | 75.58M | 81.78M | 92.93M | 84.46M | 96.46M |
| Cash, Cash Equivalents and Short-Term Investments | 15.20M | 17.96M | 18.32M | 19.76M | 27.04M | 24.75M |
| Total Debt | 10.24M | 20.57M | 18.43M | 20.96M | 16.06M | 19.26M |
| Total Liabilities | 40.10M | 53.04M | 52.52M | 56.95M | 41.86M | 49.59M |
| Stockholders Equity | 26.12M | 22.85M | 29.60M | 36.27M | 42.81M | 46.99M |
Cash Flow | ||||||
| Free Cash Flow | 6.71M | -791.90K | 5.64M | 6.38M | 5.99M | 3.30M |
| Operating Cash Flow | 6.83M | -612.19K | 6.09M | 8.45M | 6.34M | 5.42M |
| Investing Cash Flow | -1.66M | 57.84K | -105.69K | -13.67M | -501.89K | -1.76M |
| Financing Cash Flow | -7.44M | 196.90K | -7.42M | -2.06M | -3.55M | -7.12M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
53 Neutral | $76.04M | -2.47 | -24.48% | ― | 9.21% | 58.12% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $58.93M | -15.40 | -13.08% | ― | 12.21% | 69.91% | |
47 Neutral | $98.67M | -0.23 | -114.52% | ― | -86.05% | 24.17% | |
45 Neutral | $30.42M | -1.29 | -53.29% | ― | -65.77% | 38.61% | |
42 Neutral | $40.59M | -6.27 | -16.67% | ― | -23.60% | -179.33% | |
40 Underperform | $12.27M | -0.07 | ― | ― | ― | 52.39% |
On February 4, 2026, Cumberland Pharmaceuticals announced that the U.S. Food and Drug Administration granted Fast Track Designation to its oral thromboxane receptor antagonist ifetroban, which targets a fatal form of heart disease in Duchenne muscular dystrophy patients. The designation, which follows prior Orphan Drug and Rare Pediatric Disease status for ifetroban and is supported by positive Phase 2 data showing a 5.4% improvement in left ventricular ejection fraction over 12 months, is expected to accelerate regulatory interactions and review, potentially strengthening Cumberland’s position in rare disease cardiology and offering new hope in an area where no approved therapies currently exist for DMD-related heart disease.
The most recent analyst rating on (CPIX) stock is a Hold with a $4.00 price target. To see the full list of analyst forecasts on Cumberland Pharmaceuticals stock, see the CPIX Stock Forecast page.