| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 741.17M | 761.41M | 675.04M | 482.38M | 401.86M | 365.98M |
| Gross Profit | 727.78M | 748.43M | 664.16M | 475.89M | 396.47M | 360.70M |
| EBITDA | 72.46M | 68.35M | 138.29M | 108.32M | 113.89M | 127.95M |
| Net Income | 105.19M | 98.17M | 139.73M | 106.14M | 101.42M | 112.51M |
Balance Sheet | ||||||
| Total Assets | 823.61M | 836.65M | 840.55M | 621.52M | 583.43M | 423.76M |
| Cash, Cash Equivalents and Short-Term Investments | 421.68M | 372.15M | 383.33M | 368.22M | 431.67M | 223.53M |
| Total Debt | 6.36M | 6.11M | 6.94M | 151.00K | 1.14M | 526.00K |
| Total Liabilities | 191.71M | 188.85M | 160.96M | 114.81M | 81.59M | 47.95M |
| Stockholders Equity | 631.90M | 647.80M | 679.59M | 506.70M | 501.84M | 375.81M |
Cash Flow | ||||||
| Free Cash Flow | 162.57M | 141.78M | 195.90M | 126.90M | 119.91M | 167.42M |
| Operating Cash Flow | 162.85M | 142.00M | 198.07M | 127.04M | 120.32M | 167.89M |
| Investing Cash Flow | 17.24M | 69.76M | -177.60M | 90.91M | -114.33M | 136.13M |
| Financing Cash Flow | -193.71M | -220.37M | -28.35M | -148.72M | -17.28M | -302.59M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
73 Outperform | $10.56B | -28.64 | -9.06% | ― | 4.14% | -179.96% | |
67 Neutral | $3.84B | 41.68 | 16.47% | ― | 17.92% | -26.13% | |
55 Neutral | $20.27B | -20.23 | -60.76% | ― | -100.00% | -44.24% | |
53 Neutral | $6.58B | -31.79 | -240.36% | ― | 54.92% | 28.47% | |
52 Neutral | $8.69B | -46.00 | -275.50% | ― | 65.83% | 28.50% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $3.60B | -14.93 | -22.60% | ― | 74.91% | 31.54% |
On February 24, 2026, Corcept Therapeutics reported audited fourth-quarter and full-year 2025 results, with revenue rising to $202.1 million in the quarter and $761.4 million for the year, driven by stronger demand in its Cushing’s syndrome business despite supply and pharmacy transition constraints. Full-year 2025 net income declined to $99.7 million from $141.2 million in 2024, cash and investments fell to $532.4 million as the company spent $245.9 million on share repurchases, and management issued 2026 revenue guidance of $900 million to $1 billion, signaling confidence in long-term growth.
The company highlighted significant clinical and regulatory momentum, including ongoing engagement with the FDA following a Complete Response Letter for relacorilant in Cushing’s syndrome and active review of its NDA for relacorilant plus nab-paclitaxel in platinum-resistant ovarian cancer, supported by Phase 3 ROSELLA data showing a 35 percent reduction in risk of death. Across oncology, MASH and ALS, Corcept is advancing multiple mid- and late-stage trials — including the MONARCH Phase 2b MASH study, BELLA and other solid tumor programs, and a planned Phase 3 dazucorilant ALS trial — positioning the company for potential new indications that could broaden its revenue base and reinforce its standing in cortisol-modulating therapies.
The most recent analyst rating on (CORT) stock is a Buy with a $67.00 price target. To see the full list of analyst forecasts on Corcept Therapeutics stock, see the CORT Stock Forecast page.
On February 19, 2026, Corcept Therapeutics announced that the U.S. Court of Appeals for the Federal Circuit ruled Teva Pharmaceuticals’ marketing of a generic version of Korlym does not infringe two Corcept patents covering methods of safely co-administering Korlym with CYP3A4-inhibiting drugs commonly used by patients with Cushing’s syndrome. The decision upholds a December 2023 verdict from the Federal District Court for the District of New Jersey, potentially clearing a key legal hurdle for Teva’s generic Korlym product and raising competitive and revenue implications for Corcept’s flagship hypercortisolism therapy.
Corcept’s chief executive officer, Joseph K. Belanoff, M.D., expressed disappointment with the ruling, emphasizing that the asserted patents protect treatment methods relied on daily by physicians treating Cushing’s syndrome. He stated that the company will vigorously defend its intellectual property rights and is evaluating options for further judicial review, signaling an ongoing legal strategy as Corcept seeks to protect market exclusivity and manage the impact of generic competition on its Korlym franchise.
The most recent analyst rating on (CORT) stock is a Buy with a $100.00 price target. To see the full list of analyst forecasts on Corcept Therapeutics stock, see the CORT Stock Forecast page.
On January 22, 2026, Corcept Therapeutics reported that its pivotal Phase 3 ROSELLA trial of relacorilant plus nab-paclitaxel in patients with platinum-resistant ovarian cancer met its overall survival primary endpoint, with the combination reducing the risk of death by 35% versus nab-paclitaxel alone and extending median overall survival to 16.0 months from 11.9 months, without adding safety burden compared with chemotherapy alone. The trial, which previously met its progression-free survival primary endpoint and enrolled 381 patients across multiple regions, strengthens relacorilant’s clinical profile as an oral, biomarker-agnostic therapy that could reshape the treatment landscape for platinum-resistant ovarian cancer and supports Corcept’s ongoing regulatory reviews in the U.S. and Europe, as well as its broader development strategy for relacorilant and other cortisol modulators in solid tumors and hypercortisolism.
The most recent analyst rating on (CORT) stock is a Buy with a $90.00 price target. To see the full list of analyst forecasts on Corcept Therapeutics stock, see the CORT Stock Forecast page.
On December 31, 2025, Corcept Therapeutics announced that the U.S. Food and Drug Administration issued a Complete Response Letter for its New Drug Application seeking approval of relacorilant to treat patients with hypertension secondary to hypercortisolism, despite the agency acknowledging that the pivotal GRACE trial met its primary endpoint and that the GRADIENT trial provided confirmatory evidence. The FDA concluded it could not yet make a favorable benefit-risk assessment without additional evidence of effectiveness, a setback that delays U.S. commercialization of relacorilant in hypercortisolism even as the company continues to advance the drug for other indications, including platinum-resistant ovarian cancer, where it has an FDA PDUFA decision date set for July 11, 2026 and a marketing application under review in Europe.
The most recent analyst rating on (CORT) stock is a Hold with a $95.00 price target. To see the full list of analyst forecasts on Corcept Therapeutics stock, see the CORT Stock Forecast page.