| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 429.00M | 316.00M | 617.00M | 1.09B | 559.00M |
| Gross Profit | 171.00M | 185.00M | 337.00M | 662.00M | 374.00M |
| EBITDA | -822.00M | -1.75B | -635.00M | -1.94B | -1.92B |
| Net Income | -876.00M | -1.94B | -1.11B | -2.55B | -2.48B |
Balance Sheet | |||||
| Total Assets | 2.15B | 1.36B | 2.23B | 3.13B | 3.14B |
| Cash, Cash Equivalents and Short-Term Investments | 1.39B | 886.00M | 728.00M | 803.00M | 714.00M |
| Total Debt | 159.00M | 25.00M | 60.00M | 37.00M | 84.00M |
| Total Liabilities | 392.00M | 206.00M | 354.00M | 472.00M | 557.00M |
| Stockholders Equity | 1.75B | 1.16B | 1.88B | 2.66B | 2.59B |
Cash Flow | |||||
| Free Cash Flow | -847.00M | -1.03B | -359.00M | -2.48B | -2.64B |
| Operating Cash Flow | -847.00M | -1.03B | -359.00M | -2.07B | -2.47B |
| Investing Cash Flow | -81.00M | 0.00 | 2.00M | -418.00M | -164.00M |
| Financing Cash Flow | 1.43B | 1.18B | 275.00M | 2.57B | 361.00M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
66 Neutral | ¥15.07B | 16.38 | ― | ― | -5.41% | ― | |
64 Neutral | ¥6.40B | 11.74 | ― | 3.21% | 4.25% | ― | |
52 Neutral | ¥11.96B | -1.92 | ― | ― | -50.27% | -3.33% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | ¥8.08B | -8.59 | -90.96% | ― | 243.16% | -23.00% | |
48 Neutral | ¥6.27B | -7.40 | ― | ― | 56.17% | -11.63% | |
41 Neutral | ¥4.90B | -2.08 | ― | ― | ― | 47.43% |
Solasia Pharma has provided an update on its oncology and supportive care pipeline alongside its 2025 results, highlighting progress in marketed products and early-stage technology projects. The company is advancing nucleic acid medicine for peritoneal dissemination, RNA editing-based gene therapy, novel antibody modification drug discovery, and fluorescent probe technologies through collaborations with multiple research partners.
In China, Solasia’s antiemetic patch Sancuso has resumed supply following a manufacturing site transfer, with a new licensing deal granting MAAB manufacturing and marketing rights across Greater China and commercial sales slated to start in early 2027. The drug’s competitive positioning was reinforced by Phase III data published in The Oncologist, showing superiority over palonosetron in preventing delayed chemotherapy-induced nausea and vomiting.
For its lymphoma drug DARVIAS, Solasia is expanding global reach via out-licensing, including approvals for sales in Japan, ongoing NDAs in Colombia and Peru, and new commercialization rights in 13 Eastern European countries under a Managed Access Program. The company is also pursuing indication expansions into EBV-positive B-cell lymphoma and breast cancer, supported by recent scientific presentations on efficacy reassessment and mechanism of action, underscoring its strategy to broaden the clinical and commercial footprint of its key oncology asset.
The most recent analyst rating on (JP:4597) stock is a Hold with a Yen29.00 price target. To see the full list of analyst forecasts on Solasia Pharma KK stock, see the JP:4597 Stock Forecast page.
Solasia Pharma reported a 35.4% year-on-year increase in consolidated sales to ¥429 million for the fiscal year ended December 31, 2025, but continued to post an operating loss of ¥861 million and a net loss attributable to owners of the parent of ¥876 million. Despite the ongoing losses, the company’s equity position strengthened, with total assets rising to ¥2,145 million, equity attributable to owners of the parent increasing to ¥1,752 million, and cash and cash equivalents climbing to ¥1,387 million, supported by financing activities and a capital structure that remains largely equity-based.
Management again opted against paying dividends for 2025 and maintained a zero-dividend forecast for 2026, signaling a priority on preserving cash to fund operations and development activities. Solasia also refrained from issuing a numerical earnings forecast for the year ending December 31, 2026, citing difficulty in providing a reasonable estimate, which may leave investors with limited visibility into the company’s near-term earnings trajectory even as its balance sheet shows improved liquidity and capital adequacy.
The most recent analyst rating on (JP:4597) stock is a Hold with a Yen29.00 price target. To see the full list of analyst forecasts on Solasia Pharma KK stock, see the JP:4597 Stock Forecast page.
Solasia Pharma has updated investors on the status of its key pipeline and marketed products alongside its 2025 financial results, highlighting progress in commercialization and regional partnerships. In China, sales of Sancuso for chemotherapy-induced nausea and vomiting are now led by Lee’s Pharmaceutical following Solasia’s exit from direct sales, and a new license deal with MAAB will shift manufacturing and marketing rights across Greater China with commercial rollout targeted for 2027, supported by fresh Phase III data showing superiority over palonosetron.
For its oncology therapy DARVIAS, approved in Japan for relapsed or refractory peripheral T-cell lymphoma, Solasia is expanding its global reach through licensing in South America and Eastern Europe, where new NDAs have been filed or accepted and a fresh MAP-based commercialization agreement has been signed. The company is also pursuing indication expansion into EBV-positive B-cell lymphoma and breast cancer, and continues to invest in earlier-stage nucleic acid, gene therapy, antibody modification, and diagnostic probe projects, underscoring a strategy to broaden its oncology pipeline and strengthen long-term growth prospects.
The most recent analyst rating on (JP:4597) stock is a Hold with a Yen29.00 price target. To see the full list of analyst forecasts on Solasia Pharma KK stock, see the JP:4597 Stock Forecast page.
Solasia Pharma reported a 35.4% year-on-year increase in consolidated sales to ¥429 million for the fiscal year ended December 31, 2025, while narrowing its operating loss to ¥861 million and net loss attributable to owners of the parent to ¥876 million. The company strengthened its financial position with total assets rising to ¥2,145 million, equity attributable to owners of the parent climbing to ¥1,752 million, and cash and cash equivalents increasing to ¥1,387 million on the back of positive financing cash flow, though it maintained a zero-dividend policy and withheld a forecast for 2026 due to difficulty in providing a reasonable outlook.
The most recent analyst rating on (JP:4597) stock is a Hold with a Yen29.00 price target. To see the full list of analyst forecasts on Solasia Pharma KK stock, see the JP:4597 Stock Forecast page.
Solasia Pharma has signed a license agreement granting MAAB Pharma exclusive marketing and manufacturing rights for its antiemetic patch Sancuso in mainland China, Hong Kong, Macau and Taiwan, as part of a restructuring of its sales framework in the region. After the current commercialization agreement with Lee’s Pharmaceutical in mainland China expires at the end of 2026, sales activities will transfer to MAAB, which plans to establish local production to lower costs, while Solasia will receive staged contract payments tied to the business transfer and future royalties on sales, positioning MAAB as a key strategic partner for Solasia’s broader China business and potentially improving the product’s competitiveness and profitability in that market.
The most recent analyst rating on (JP:4597) stock is a Hold with a Yen29.00 price target. To see the full list of analyst forecasts on Solasia Pharma KK stock, see the JP:4597 Stock Forecast page.
Solasia Pharma has revised downward its full-year earnings forecast for the fiscal year ending December 2025, cutting projected sales revenue by ¥900 million to ¥400 million. The revision is driven primarily by delays in recognizing product sales of Sancuso in China due to extended customs and testing procedures following a manufacturing site change, the termination of a license agreement with FIREBIRD BIOLOGICS that eliminates expected upfront and milestone payments for DARVIAS and Episil, and the decision to exclude from its outlook any revenue tied to yet-unconcluded technology transfer and commercial license agreements for Sancuso in China beyond 2026. In addition, the company will return part of unrecognized upfront revenue from a Chinese Episil license with GenSci, though this will not affect profit or loss, underscoring that the main impact of these changes is a near-term revenue shortfall rather than an immediate hit to reported earnings, and highlighting ongoing uncertainty around the timing and structure of Solasia’s China-related partnership income.