| Breakdown | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | May 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 0.00 | 587.00K | 542.00K | 219.00K | 690.86K |
| Gross Profit | 0.00 | -134.00K | -51.00K | 55.00K | 517.72K |
| EBITDA | -1.38M | -2.94M | -2.59M | -900.00K | -322.29K |
| Net Income | -1.59M | -3.12M | -2.71M | -954.00K | -274.29K |
Balance Sheet | |||||
| Total Assets | 3.20M | 2.43M | 4.94M | 3.13M | 2.77M |
| Cash, Cash Equivalents and Short-Term Investments | 757.00K | 155.00K | 1.64M | 598.00K | 209.00K |
| Total Debt | 0.00 | 34.00K | 22.00K | 950.00K | 654.00K |
| Total Liabilities | 119.00K | 408.00K | 385.00K | 2.32M | 1.22M |
| Stockholders Equity | 3.08M | 2.03M | 4.55M | 812.00K | 1.54M |
Cash Flow | |||||
| Free Cash Flow | -1.13M | -1.47M | -3.08M | -255.00K | -15.00K |
| Operating Cash Flow | -1.13M | -1.24M | -2.36M | -254.00K | 1.00K |
| Investing Cash Flow | -337.00K | -232.00K | -718.00K | -1.00K | -16.00K |
| Financing Cash Flow | 2.08M | 0.00 | 4.13M | 800.00K | 199.00K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
74 Outperform | £6.56B | 20.02 | 24.91% | 1.29% | -0.32% | -3.96% | |
70 Outperform | £179.65M | 10.69 | 6.13% | 1.02% | 14.49% | 76.33% | |
66 Neutral | £7.40B | 29.17 | 13.46% | 1.93% | -6.93% | 18.57% | |
63 Neutral | $10.79B | 15.43 | 7.44% | 2.01% | 2.89% | -14.66% | |
62 Neutral | £555.19M | 28.89 | 8.04% | 4.87% | -7.30% | -59.71% | |
61 Neutral | £87.96M | -2.99 | -17.46% | ― | 21.17% | -237.25% | |
50 Neutral | £16.34M | ― | -62.23% | ― | ― | ― |
Solvonis Therapeutics has selected SVN‑114 as the lead candidate in its Post‑Traumatic Stress Disorder discovery programme, following preclinical work showing balanced modulation of serotonin, dopamine and noradrenaline systems. The compound comes from the company’s proprietary SVN‑SDN‑14 series, designed to enhance pro‑social behaviour and improve engagement with therapy in patients with PTSD, a condition with limited effective pharmacological options.
SVN‑114 is supported by international composition‑of‑matter patent applications covering both the chemical class and its therapeutic uses, giving Solvonis a strong intellectual property position in trauma‑related psychiatric disorders. Management and scientific leadership say the decision marks a key milestone for the company’s CNS discovery platform and could help position Solvonis for first‑ or best‑in‑class treatments in a large, underserved and growing global mental‑health market.
The most recent analyst rating on (GB:SVNS) stock is a Hold with a £0.26 price target. To see the full list of analyst forecasts on Solvonis Therapeutics stock, see the GB:SVNS Stock Forecast page.
Solvonis Therapeutics has expanded development of its investigational compound SVN‑015 into depression after preclinical studies in validated rodent behavioural models showed antidepressant‑like activity comparable to the widely used SSRI fluoxetine following 14 days of once‑daily dosing. SVN‑015, a novel serotonin‑dopamine reuptake inhibitor designed for once‑daily oral use at home, is being positioned as a potential new class of antidepressant particularly for patients with inadequate response to SSRIs, targeting symptoms such as anhedonia and reduced motivation, and its progress adds to Solvonis’s broader CNS franchise, which also includes NIDA‑backed work in stimulant use disorders and could strengthen the company’s positioning and partnering prospects in the competitive market for mood and addiction therapies.
The most recent analyst rating on (GB:SVNS) stock is a Hold with a £0.27 price target. To see the full list of analyst forecasts on Solvonis Therapeutics stock, see the GB:SVNS Stock Forecast page.
Solvonis Therapeutics has received a Notice of Allowance from the U.S. Patent and Trademark Office covering a novel series of compounds within its SVN-SDN-14 PTSD discovery programme, bolstering the intellectual property position of this early-stage asset as the company moves toward selecting a lead candidate in the first quarter of 2026. The newly protected compounds are designed to modulate serotonin, dopamine and noradrenaline pathways while offering improved pharmacokinetic control through predictable metabolic deactivation, a feature the company says could translate into safer, more flexible dosing and greater real-world clinical utility, strengthening both the scientific validation and commercial prospects of Solvonis’s PTSD franchise in the competitive CNS therapeutics landscape.
The most recent analyst rating on (GB:SVNS) stock is a Hold with a £0.32 price target. To see the full list of analyst forecasts on Solvonis Therapeutics stock, see the GB:SVNS Stock Forecast page.
Solvonis Therapeutics reported broad progress across its CNS pipeline as it heads into what it describes as a catalyst-rich 2026, highlighting advancement of its lead alcohol use disorder (AUD) and PTSD programmes alongside AI-driven discovery efforts. Lead candidate SVN-001 is moving through a potentially pivotal Phase 3 trial for severe AUD in a large, underserved UK and EU population, while SVN-002, an esketamine oral thin film for moderate-to-severe AUD, is being prepared for a U.S. Phase 2b trial via an FDA 505(b)(2) pathway that could materially reduce development time and cost. The company also secured external validation for its AI-enabled platform with SVN-015’s acceptance into the U.S. National Institute on Drug Abuse’s Addiction Treatment Discovery Program, which brings NIDA-funded preclinical work and potential access to further non-dilutive NIH development funding for stimulant use disorder. Meanwhile, PTSD candidate SVN-SDN-14 is nearing lead selection ahead of IND-enabling studies, and Solvonis says the integration of Awakn Life Sciences earlier in 2025 has created a more diversified CNS platform, positioning the group with multiple regulatory, preclinical and partnering milestones that could enhance both its industry standing in addiction psychiatry and its long-term value proposition for shareholders.