| Breakdown | Jul 2025 | Jul 2024 | Jul 2023 | Jul 2022 | Jul 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 0.00 | 0.00 | 2.35B | 22.98M | 1.40B |
| Gross Profit | -49.50M | -44.35M | 2.30B | 0.00 | 0.00 |
| EBITDA | -1.92B | -2.03B | 190.18M | -1.93B | -550.13M |
| Net Income | -1.93B | -2.02B | 168.35M | -1.95B | -582.45M |
Balance Sheet | |||||
| Total Assets | 7.52B | 9.09B | 10.72B | 9.61B | 10.93B |
| Cash, Cash Equivalents and Short-Term Investments | 6.99B | 8.41B | 10.22B | 8.88B | 10.17B |
| Total Debt | 0.00 | 0.00 | 531.00K | 3.67M | 6.73M |
| Total Liabilities | 210.27M | 194.06M | 348.51M | 207.74M | 231.10M |
| Stockholders Equity | 7.31B | 8.89B | 10.37B | 9.40B | 10.70B |
Cash Flow | |||||
| Free Cash Flow | -1.46B | -1.88B | 1.14B | -1.40B | -608.70M |
| Operating Cash Flow | -1.41B | -1.88B | 1.14B | -1.40B | -519.65M |
| Investing Cash Flow | -42.50M | -4.78M | -344.00K | -330.00K | -92.72M |
| Financing Cash Flow | 41.25M | 78.97M | 202.60M | 112.86M | 109.32M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
57 Neutral | ¥7.96B | 59.41 | ― | 1.24% | -14.78% | -95.53% | |
56 Neutral | ¥16.02B | 120.78 | ― | ― | 1.24% | -33.41% | |
54 Neutral | ¥24.81B | -34.16 | ― | ― | -5.65% | -469.19% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | ¥53.60B | -13.30 | ― | ― | -82.33% | 47.73% | |
49 Neutral | ¥12.00B | -8.14 | ― | ― | -42.49% | -2.37% | |
43 Neutral | ¥18.55B | -11.30 | ― | ― | ― | 11.34% |
StemRIM Inc. released presentation materials outlining its financial results for the six months ended January 31, 2026 and provided an overview of management indicators, financial summaries, and key business highlights. The update also detailed progress in research and development, advances in its regeneration-inducing medicine platform, IP strategy, and business development activities, indicating continued execution of its growth and innovation plans in regenerative therapeutics.
The most recent analyst rating on (JP:4599) stock is a Hold with a Yen299.00 price target. To see the full list of analyst forecasts on StemRIM Inc. stock, see the JP:4599 Stock Forecast page.
StemRIM reported no operating revenue and a net loss of ¥928 million for the six months to Jan. 31, 2026, narrowing slightly from the previous year’s ¥1,048 million loss as basic loss per share improved to ¥14.91. Total assets fell to ¥6,812 million and the equity ratio declined to 74.6%, while the company again declared no interim dividend and has withheld a full-year earnings forecast due to the volatility of milestone income.
Management said it will continue advancing its flagship Regeneration-Inducing Medicine candidate Redasemtide and subsequent pipeline assets toward clinical development and out-licensing, with forecast cash R&D spending of ¥1.3–1.7 billion and SG&A of ¥230–310 million in the current fiscal year. StemRIM noted potential upfront and milestone payments from new and existing partnerships but emphasized it has already secured sufficient funding to support its research and development activities through 2028, offering some visibility for investors despite ongoing losses and uncertain revenue timing.
The most recent analyst rating on (JP:4599) stock is a Hold with a Yen280.00 price target. To see the full list of analyst forecasts on StemRIM Inc. stock, see the JP:4599 Stock Forecast page.
StemRIM Inc. announced that a Japanese patent has been granted for a stem cell gene therapy technology, SR-GT1, designed to provide a curative treatment for dystrophic epidermolysis bullosa, a severe hereditary skin disorder caused by defects in type VII collagen. The patent covers the therapeutic approach of administering genetically corrected autologous mesenchymal stem cells into patients’ blisters, supporting long-term collagen production to restore skin integrity.
The newly secured intellectual property strengthens StemRIM’s technological base for treating recessive dystrophic epidermolysis bullosa and complements its existing portfolio developed with Osaka University. SR-GT1 is being produced as an investigational drug with support from Japan’s AMED, and preparations for an early transition to a physician-led clinical trial are progressing, though the company expects no material impact on earnings for the current fiscal year.
The most recent analyst rating on (JP:4599) stock is a Hold with a Yen302.00 price target. To see the full list of analyst forecasts on StemRIM Inc. stock, see the JP:4599 Stock Forecast page.
StemRIM Inc. has secured a forthcoming Canadian patent covering the use of its peptide drug candidate Redasemtide, an HMGB1 fragment peptide, as a therapeutic agent for a broad spectrum of cartilage disorders including osteoarthritis, meniscal damage, and certain forms of arthritis. The patent expands potential indications for Redasemtide in Canada and supports the company’s strategy to develop an intravenously administered, low-burden regenerative treatment that mobilizes mesenchymal stem cells to sites of cartilage injury, although StemRIM expects no material impact on its financial results for the fiscal year ending July 31, 2026.
By reinforcing Redasemtide’s intellectual property position in a key market, the move underpins StemRIM’s efforts to establish its regeneration-inducing platform in orthopedic and joint disease segments where current therapies are often limited and conditions are typically chronic and progressive. The additional protection may enhance the company’s competitive standing in cartilage repair therapies and provide long-term optionality for partnerships or future commercialization, while short-term financial effects remain minimal.
The most recent analyst rating on (JP:4599) stock is a Hold with a Yen281.00 price target. To see the full list of analyst forecasts on StemRIM Inc. stock, see the JP:4599 Stock Forecast page.
StemRIM Inc. announced that partner Shionogi & Co. has completed patient enrollment in a global Phase 2b clinical trial of Redasemtide (S‑005151), a peptide drug derived from StemRIM’s “Regeneration-Inducing Medicine” platform, for adults with acute ischemic stroke treated within 25 hours of onset. The trial, conducted across 18 countries including Japan, the U.S. and European states, is evaluating the efficacy and safety of Redasemtide versus placebo—with or without endovascular recanalization—using the 90-day modified Rankin Scale as the primary endpoint; the company noted the program is progressing as planned and is not expected to affect full-year earnings for the fiscal year ending July 2026, underscoring steady advancement of its lead regenerative therapeutic without near-term financial disruption.