| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 7.50M | 0.00 | 0.00 | 9.43M | 18.44M |
| Gross Profit | 0.00 | -2.56M | -167.51M | 9.43M | 18.44M |
| EBITDA | -342.35M | -235.86M | -210.51M | -127.74M | -78.09M |
| Net Income | -345.91M | -234.33M | -182.39M | -125.37M | -78.88M |
Balance Sheet | |||||
| Total Assets | 633.16M | 798.14M | 964.80M | 754.15M | 572.01M |
| Cash, Cash Equivalents and Short-Term Investments | 548.89M | 626.90M | 638.08M | 592.09M | 551.77M |
| Total Debt | 7.94M | 9.02M | 10.90M | 10.44M | 8.26M |
| Total Liabilities | 51.40M | 43.24M | 36.88M | 32.65M | 21.97M |
| Stockholders Equity | 633.16M | 754.90M | 927.92M | 721.50M | 550.03M |
Cash Flow | |||||
| Free Cash Flow | -279.92M | -184.46M | -150.94M | -101.32M | -71.55M |
| Operating Cash Flow | -279.12M | -181.39M | -145.33M | -98.43M | -69.50M |
| Investing Cash Flow | 218.00M | 165.00M | -117.17M | -296.00M | -246.77M |
| Financing Cash Flow | 117.11M | 12.13M | 353.52M | 278.47M | 447.54M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
63 Neutral | $3.60B | -9.91 | -45.14% | ― | ― | -38.30% | |
62 Neutral | $5.64B | -10.34 | -69.35% | ― | ― | -27.70% | |
52 Neutral | $3.91B | -10.63 | -47.34% | ― | ― | -126.16% | |
52 Neutral | $2.32B | -9.89 | -42.14% | ― | ― | 9.60% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $4.52B | -13.62 | -218.04% | ― | ― | -31.71% | |
46 Neutral | $2.26B | -4.01 | -656.54% | ― | 20.63% | 8.09% |
On Feb. 26, 2026, Xenon Pharmaceuticals reported its fourth-quarter and full-year 2025 results, highlighting heavy investment in late-stage development of azetukalner across epilepsy and neuropsychiatric indications. The company is advancing multiple Phase 3 programs, including X-TOLE2 and X-TOLE3 in focal onset seizures, X-ACKT in primary generalized tonic-clonic seizures, and X-NOVA and X-CEED in depression and bipolar disorder, supported by 48‑month open-label data showing sustained seizure reduction and long-term safety.
Xenon is also progressing early-stage NaV1.7 and KV7 candidates XEN1701 and XEN1120 in Phase 1 pain studies and continuing IND-enabling work on a NaV1.1 program for Dravet syndrome, while its partnered NaV1.2/NaV1.6 inhibitor with Neurocrine remains in Phase 1. To fund this pipeline, the company raised $242.2 million via at-the-market equity sales, ending 2025 with $586 million in cash and pro forma liquidity of $716 million, which it expects will support operations into the second half of 2027 despite a 2025 net loss of $345.9 million driven by expanded R&D and higher operating costs.
The most recent analyst rating on (XENE) stock is a Buy with a $62.00 price target. To see the full list of analyst forecasts on Xenon stock, see the XENE Stock Forecast page.
On November 24, 2025, Xenon Pharmaceuticals Inc. amended its 2025 Inducement Equity Incentive Plan to increase the number of shares reserved for issuance from 775,000 to 900,000. This adjustment is intended to facilitate the granting of various stock-related incentives to new or returning employees without requiring shareholder approval, in line with Nasdaq Listing Rule 5635(c)(4).
The most recent analyst rating on (XENE) stock is a Buy with a $44.00 price target. To see the full list of analyst forecasts on Xenon stock, see the XENE Stock Forecast page.