| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 4.71M | 4.71M | 0.00 | 5.27M | 0.00 | 0.00 |
| Gross Profit | 3.59M | 3.59M | -966.00K | 4.75M | -740.00K | -249.00K |
| EBITDA | -12.71M | -12.71M | -7.06M | -12.19M | -3.75M | -14.90M |
| Net Income | -12.27M | -12.27M | -5.86M | -11.94M | -2.06M | -15.48M |
Balance Sheet | ||||||
| Total Assets | 23.09M | 23.09M | 23.58M | 30.27M | 49.06M | 8.82M |
| Cash, Cash Equivalents and Short-Term Investments | 16.89M | 16.89M | 14.82M | 19.92M | 28.73M | 41.11M |
| Total Debt | 16.27M | 16.27M | 19.87M | 21.13M | 18.92M | 15.39M |
| Total Liabilities | 26.93M | 26.93M | 27.08M | 36.50M | 29.57M | 1.17M |
| Stockholders Equity | -3.83M | -3.83M | -3.50M | -6.23M | 18.11M | 19.48M |
Cash Flow | ||||||
| Free Cash Flow | -6.12M | -6.12M | -15.84M | -8.34M | -8.55M | -4.80M |
| Operating Cash Flow | -6.11M | -6.11M | -15.66M | -8.14M | -7.80M | -4.77M |
| Investing Cash Flow | -1.54M | -1.54M | 178.00K | 81.00K | -741.00K | -13.00K |
| Financing Cash Flow | 9.73M | 9.73M | 10.39M | -746.00K | 46.08M | 46.08M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
56 Neutral | £31.15M | -3.73 | -204.29% | ― | 3.31% | 21.91% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | £34.79M | -4.43 | -46.84% | ― | ― | ― | |
48 Neutral | £121.94M | -8.98 | ― | ― | ― | -94.12% | |
47 Neutral | £27.61M | -5.93 | -202.14% | ― | ― | 23.76% | |
41 Neutral | £91.36M | -5.94 | -209.34% | ― | 198.49% | -26.66% | |
37 Underperform | £41.47M | -2.02 | ― | ― | 63.25% | 8.94% |
Scancell Holdings has announced positive updated data from its SCOPE Phase 2 trial, demonstrating that its iSCIB1+ therapy, in combination with standard checkpoint inhibitors, significantly improves progression-free survival (PFS) in patients with advanced melanoma. The PFS rate of 74% at 16 months surpasses the standard of care’s 50% at 11.5 months, and early overall survival data shows a 14% improvement. These results support further development of iSCIB1+ for late-stage trials, with regulatory feedback aligning on trial design and endpoints. The announcement positions Scancell favorably in the immunotherapy market, potentially redefining the standard of care for melanoma and enhancing patient outcomes.
Scancell Holdings announced positive Phase 2 trial results for their iSCIB1+ Immunobody® DNA active immunotherapy in treating late-stage melanoma, presented at the SITC 2025 meeting. The trial showed a progression-free survival rate of 78% at 11 months, significantly higher than the historical 46% with existing therapies, positioning iSCIB1+ as a transformative treatment option. The company plans to accelerate development, including regulatory discussions and randomized studies set to begin in 2026, potentially expanding treatment to 80% of late-stage melanoma patients.
Scancell Holdings announced that all resolutions at their Annual General Meeting were passed, marking a positive step for the company. This development supports Scancell’s ongoing efforts in advancing their immunotherapy platforms, which could enhance their position in the biotechnology industry and benefit stakeholders by potentially offering innovative cancer treatments.