| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 56.00K | 113.00K | 2.85M | 9.65M | 2.94M | 2.14M |
| Gross Profit | -682.00K | 113.00K | 2.84M | 4.23M | -2.50M | -973.00K |
| EBITDA | -12.03M | -17.62M | -14.12M | -34.78M | -26.69M | -16.40M |
| Net Income | -17.02M | -52.84M | -24.95M | -36.94M | -26.32M | -18.89M |
Balance Sheet | ||||||
| Total Assets | 29.24M | 48.27M | 73.19M | 92.65M | 47.00M | 67.46M |
| Cash, Cash Equivalents and Short-Term Investments | 12.64M | 12.87M | 16.63M | 41.78M | 26.19M | 47.91M |
| Total Debt | 20.40M | 22.93M | 23.51M | 62.94M | 1.70M | 2.04M |
| Total Liabilities | 29.09M | 38.99M | 51.39M | 74.21M | 5.78M | 5.53M |
| Stockholders Equity | 144.00K | 9.28M | 21.80M | 18.44M | 41.22M | 61.93M |
Cash Flow | ||||||
| Free Cash Flow | -13.55M | -23.94M | -16.13M | -17.03M | -21.82M | -12.31M |
| Operating Cash Flow | -13.51M | -23.60M | -14.87M | -16.43M | -20.51M | -10.64M |
| Investing Cash Flow | 8.77M | -1.43M | -9.00M | -25.04M | 18.70M | -21.90M |
| Financing Cash Flow | 666.00K | 26.09M | -1.30M | 56.90M | 232.00K | 51.65M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
56 Neutral | £30.77M | -3.69 | -204.29% | ― | 3.31% | 21.91% | |
55 Neutral | £319.99M | 9.27 | 15.04% | ― | 1231.50% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | £137.51M | -25.00 | ― | ― | ― | -94.12% | |
46 Neutral | £4.01M | -4.75 | -153.80% | ― | ― | -616.67% | |
42 Neutral | £225.26M | ― | ― | ― | ― | ― | |
41 Neutral | £89.04M | -5.79 | -209.34% | ― | 198.49% | -26.66% |
Avacta Group plc has secured U.S. Food and Drug Administration clearance for its Investigational New Drug application for FAP-Exatecan (AVA6103), the company’s second pre|CISION® medicine and its first peptide drug conjugate using the potent topoisomerase I inhibitor exatecan. The IND approval allows Avacta to advance AVA6103 from preclinical work into a Phase 1 clinical trial in the U.S., expected to start later in the first quarter of 2026, assessing safety, preliminary efficacy and dose in adults with pancreatic, cervical, gastric and small cell lung cancers using two dosing schedules, with initial data anticipated in the second half of 2026. Management frames the rapid 24‑month progression from program inception to IND as an important validation of the pre|CISION® platform and its sustained-release mechanism, which is designed to enhance anti-tumor activity while limiting toxicities seen with exatecan alone, potentially strengthening Avacta’s position in next-generation oncology therapeutics and providing clinical proof-of-concept that could support broader application of its capping group and linker technologies across multiple payloads.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £51.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.
Avacta reported strong operational and R&D progress in 2025, highlighting encouraging efficacy and safety data from its faridoxorubicin (AVA6000) Phase 1b expansion cohorts in salivary gland cancer and continued enrollment to refine trial design for later-stage studies. The company advanced its second pre|CISION® program, FAP-Exd (AVA6103), with supportive pharmacology data, a Phase 1 trial set to start in early 2026 across multiple U.S. specialty oncology centers in four AI-selected tumor types, and the introduction of new platform innovations including a sustained-release mechanism and a dual-payload delivery technology. Financially, Avacta raised £22.5m in equity during 2025 and ended the year with £16.9m in cash and equivalents, providing funding into the third quarter of 2026 to reach key data readouts for both AVA6000 and AVA6103 while it continues active partnering discussions that could shape the design, funding and risk profile of its subsequent pivotal trials and broader pipeline development.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £53.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.
Avacta Group plc has appointed Strand Hanson Limited as its Nominated Adviser with immediate effect, a key governance and regulatory role for companies listed on AIM, and confirmed that its issued share capital stands at 440,415,495 ordinary shares for the purposes of disclosure and transparency rules. The company also provided additional regulatory disclosures regarding past directorships of board member Richard Hughes in several companies that later entered administration, ensuring compliance with AIM Rule 17 and offering investors fuller visibility over the board’s historical corporate involvements.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £53.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.
Avacta Group plc has released promising preclinical pharmacology data for FAP-Exd (AVA6103), a tumor-activated drug designed to deliver a highly potent topoisomerase I inhibitor directly to tumors. Key findings highlighted include enhanced tumor-specific cytotoxicity, sustained drug release over five days within tumors, and durable antitumor responses in preclinical models—signifying potential benefits over conventional therapies. The use of AI in clinical trial design has further optimized development and selection of patient populations, positioning the drug for a fast-track Phase 1 trial in early 2026, with significant implications for addressing unmet needs in oncology.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £81.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.
Avacta Group PLC announced promising Phase 1b clinical trial results for its drug faridoxorubicin (AVA6000) in treating salivary gland cancer (SGC), showing a 90% disease control rate across Phase 1a and 1b trials. The trial demonstrated clinically meaningful tumor shrinkage and prolonged progression-free survival, reinforcing the potential of Avacta’s pre|CISION® platform to provide new treatment options for SGC and other solid tumors, with further data expected in the first half of 2026.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £81.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.
Avacta Group plc announced preliminary clinical data from its Phase 1b trial of Faridoxorubicin in patients with salivary gland cancer, with detailed results to be presented on December 17, 2025. This announcement marks a significant step in Avacta’s efforts to advance its PDC technology, potentially improving treatment outcomes and positioning the company as a leader in targeted cancer therapies.
The most recent analyst rating on (GB:AVCT) stock is a Hold with a £81.00 price target. To see the full list of analyst forecasts on Avacta Group plc stock, see the GB:AVCT Stock Forecast page.