| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 435.83M | 233.18M | 145.24M | 109.46M | 131.84M | 198.32M |
| Gross Profit | 425.49M | 225.43M | 133.79M | 105.04M | 128.02M | 192.19M |
| EBITDA | -22.58M | -265.77M | -326.25M | -299.42M | -184.46M | -145.16M |
| Net Income | -88.54M | -321.55M | -111.40M | -278.48M | -180.09M | -169.43M |
Balance Sheet | ||||||
| Total Assets | 538.58M | 594.13M | 788.91M | 672.59M | 776.63M | 607.44M |
| Cash, Cash Equivalents and Short-Term Investments | 254.53M | 370.70M | 566.85M | 450.25M | 552.88M | 361.59M |
| Total Debt | 329.75M | 401.58M | 404.78M | 407.49M | 261.99M | 244.03M |
| Total Liabilities | 465.02M | 535.05M | 588.10M | 629.73M | 474.52M | 396.23M |
| Stockholders Equity | 73.56M | 59.08M | 200.81M | 42.85M | 302.11M | 211.21M |
Cash Flow | ||||||
| Free Cash Flow | -80.33M | -338.69M | -321.61M | -214.66M | -38.94M | -162.59M |
| Operating Cash Flow | -58.61M | -237.47M | -280.02M | -186.29M | -14.79M | -42.74M |
| Investing Cash Flow | 52.42M | 99.33M | 55.78M | -32.55M | -137.62M | -61.33M |
| Financing Cash Flow | 78.97M | 139.42M | 218.75M | 117.57M | 231.68M | 127.71M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
60 Neutral | $3.47B | -78.36 | -28.17% | ― | 129.21% | 80.35% | |
60 Neutral | $3.30B | ― | -28.35% | ― | 182.44% | 47.21% | |
56 Neutral | $3.03B | -31.80 | -410.78% | ― | 114.22% | 77.02% | |
52 Neutral | $2.44B | -2.45 | -91.06% | ― | -32.98% | -18.46% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $2.07B | -4.25 | -16.45% | ― | ― | ― | |
43 Neutral | $3.30B | -16.88 | -34.78% | ― | ― | -34.96% |
On September 10, 2025, Travere Therapeutics announced that the FDA has decided an advisory committee is no longer needed for the review of the supplemental New Drug Application for FILSPARI in treating FSGS. The application remains under review with a target action date of January 13, 2026. If approved, FILSPARI would be the first medication indicated for FSGS, a serious kidney disorder. The drug has shown promising results in reducing proteinuria in clinical trials, which is significant for patients as it lowers the risk of kidney failure. The studies supporting FILSPARI’s application demonstrated its efficacy and safety, with results published in the New England Journal of Medicine indicating a meaningful clinical benefit.