| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 435.83M | 233.18M | 145.24M | 212.02M | 227.49M | 198.32M |
| Gross Profit | 248.20M | 181.88M | 133.79M | 204.43M | 220.71M | 192.19M |
| EBITDA | -41.90M | -265.77M | -326.25M | -299.42M | -186.68M | -143.95M |
| 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 | 215.34M |
| 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 | -68.55M | -338.69M | -322.28M | -214.85M | -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 |
|---|---|---|---|---|---|---|---|
| ― | $3.10B | ― | -28.17% | ― | 129.21% | 80.35% | |
| ― | $2.90B | ― | -31.46% | ― | 254.45% | 48.06% | |
| ― | $3.15B | ― | -410.78% | ― | 114.22% | 77.02% | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
| ― | $2.40B | ― | -86.34% | ― | 30.14% | -10.08% | |
| ― | $2.10B | ― | -10.10% | ― | ― | ― | |
| ― | $3.22B | ― | -26.36% | ― | ― | -22.19% |
Travere Therapeutics, Inc. recently held its earnings call, revealing a strong quarter marked by significant growth in FILSPARI sales, potential FDA approval for new indications, and successful manufacturing advancements. Despite these achievements, the company faces challenges from seasonal trends and a competitive market landscape.
Travere Therapeutics, Inc. is a biopharmaceutical company focused on developing and delivering therapies for rare diseases, with a notable emphasis on nephroprotective treatments.
Travere Therapeutics, Inc. is conducting a clinical study titled ‘A Multicenter, Open-label Single Arm Study to Evaluate the Safety and Efficacy of Sparsentan in Posttransplant Immunoglobulin A Nephropathy (IgAN) or Focal Segmental Glomerulosclerosis (FSGS) (SPARX)’. The study aims to assess the safety and efficacy of sparsentan tablets in treating proteinuria in patients who have undergone kidney transplantation, with a focus on IgAN and FSGS conditions.
Travere Therapeutics, Inc. is conducting a clinical study titled A Phase 2, Open-Label, Single-Arm, Cohort Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sparsentan Treatment in Pediatric Subjects With Selected Proteinuric Glomerular Diseases. The study aims to assess the safety, efficacy, and tolerability of sparsentan, focusing on its impact on proteinuria in children with specific kidney conditions over a 108-week period. This research is significant as it targets rare pediatric kidney diseases, potentially offering a new treatment option.
Study Overview: Travere Therapeutics, Inc. is conducting a Phase 3 long-term extension study titled ENSEMBLE to assess the safety, tolerability, and efficacy of Pegtibatinase in participants aged 5 to 65 with classical homocystinuria (HCU) due to cystathionine beta synthase deficiency. This study aims to provide crucial data on the long-term effects of Pegtibatinase, a promising treatment for this rare genetic disorder.
Travere Therapeutics, Inc. is conducting a study titled ‘A Multicenter, Observational, Prospective, Natural History Study of Homocystinuria Due to Cystathionine Beta-synthase Deficiency in Pediatric and Adult Patients (ACAPPELLA)’. The study aims to understand the clinical progression of homocystinuria in patients aged 1 to 65 under current management practices, providing valuable insights into this condition.
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.
The most recent analyst rating on (TVTX) stock is a Buy with a $47.00 price target. To see the full list of analyst forecasts on Travere Therapeutics stock, see the TVTX Stock Forecast page.
Travere Therapeutics, Inc. recently held its earnings call, showcasing a robust commercial performance for its leading product, FILSPARI. The call highlighted significant growth in sales, positive clinical data, and international expansion efforts. Despite challenges such as potential generic competition for THIOLA and regulatory uncertainties for FILSPARI’s approval in FSGS, the overall sentiment was optimistic, driven by FILSPARI’s strong market performance and potential.
Travere Therapeutics, Inc. is a biopharmaceutical company focused on developing and delivering life-changing therapies for patients with rare diseases. The company recently reported its second quarter 2025 financial results, highlighting significant growth in net product sales, particularly for its drug FILSPARI (sparsentan), which saw a 165% increase year-over-year.