| 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 | $3.23B | -71.79 | -28.17% | ― | 129.21% | 80.35% | |
60 Neutral | $2.89B | -31.88 | -28.35% | ― | 182.44% | 47.21% | |
56 Neutral | $2.69B | -27.92 | -410.78% | ― | 114.22% | 77.02% | |
52 Neutral | $3.10B | ― | -34.78% | ― | ― | -34.96% | |
52 Neutral | $2.39B | -2.47 | -91.06% | ― | -32.98% | -18.46% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $2.29B | -4.58 | -16.45% | ― | ― | ― |
On January 13, 2026, Travere Therapeutics announced that the U.S. Food and Drug Administration extended the review timeline for the supplemental New Drug Application for FILSPARI in focal segmental glomerulosclerosis, moving the target action date to April 13, 2026 after the company submitted additional data to further characterize the drug’s clinical benefit. The FDA classified these new materials as a Major Amendment but did not request further safety or manufacturing information, and the filing rests on clinical evidence from the large Phase 3 DUPLEX study and Phase 2 DUET study, which showed significant reductions in proteinuria and clinically meaningful benefits versus irbesartan despite DUPLEX not meeting its primary eGFR slope endpoint, underscoring both the potential of FILSPARI to become the first indicated therapy for FSGS and the regulatory scrutiny around demonstrating long‑term kidney function outcomes in this rare disease population.
The most recent analyst rating on (TVTX) stock is a Hold with a $31.00 price target. To see the full list of analyst forecasts on Travere Therapeutics stock, see the TVTX Stock Forecast page.