| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | -2.78M | -8.55M | -9.19M | -9.53M | -8.87M | -1.41M |
| EBITDA | -196.23M | -277.76M | -169.81M | -122.13M | -87.82M | -50.99M |
| Net Income | -216.42M | -285.52M | -179.67M | -130.27M | -96.70M | -52.30M |
Balance Sheet | ||||||
| Total Assets | 820.20M | 796.34M | 765.26M | 585.43M | 622.90M | 605.30M |
| Cash, Cash Equivalents and Short-Term Investments | 197.98M | 208.24M | 166.30M | 120.17M | 271.88M | 325.60M |
| Total Debt | 148.91M | 128.22M | 36.81M | 2.13M | 3.23M | 4.86M |
| Total Liabilities | 178.47M | 173.25M | 71.85M | 29.41M | 31.15M | 22.72M |
| Stockholders Equity | 641.73M | 623.10M | 693.41M | 556.02M | 591.75M | 582.59M |
Cash Flow | ||||||
| Free Cash Flow | -253.43M | -264.51M | -257.38M | -238.47M | -147.57M | -145.00M |
| Operating Cash Flow | -213.39M | -222.37M | -203.28M | -110.18M | -51.61M | -47.79M |
| Investing Cash Flow | -46.90M | -42.14M | -65.88M | -135.34M | -105.82M | -96.83M |
| Financing Cash Flow | 383.63M | 306.11M | 315.59M | 93.81M | 103.71M | 260.35M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
76 Outperform | kr3.25B | 5.12 | 167.77% | ― | 2687.51% | ― | |
64 Neutral | kr1.33B | 10.54 | 81.19% | ― | ― | ― | |
58 Neutral | kr3.36B | -6.49 | -71.87% | ― | -91.85% | -6.65% | |
56 Neutral | kr1.27B | -10.90 | -58.41% | ― | ― | 48.14% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | kr892.06M | -2.99 | ― | ― | 131.20% | 32.28% | |
42 Neutral | kr1.04B | -4.26 | -35.03% | ― | ― | 25.14% |
Xspray Pharma’s Q3 2025 report highlights significant developments, including achieving bioequivalence for its XS003 product at a reduced dosage compared to the reference drug Tasigna, and securing a license agreement with Handa Therapeutics for commercialization in the US and Asian markets. Additionally, the company raised approximately SEK 161 million through a heavily oversubscribed share issue and extended the maturity of an existing loan, enhancing its financial position.
Xspray Pharma AB announced that the FDA has accepted its New Drug Application for XS003, an improved formulation of nilotinib for treating chronic myeloid leukemia, with a PDUFA date set for June 18, 2026. This development signifies a major milestone for the company, potentially enhancing its market position in the U.S. oncology sector, with expectations of improved patient adherence due to reduced food effect and manufacturing processes already familiar to the FDA.