| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 2.35B | 22.98M | 1.40B |
| Gross Profit | -49.50M | -49.50M | -44.35M | 2.35B | 22.98M | 1.40B |
| EBITDA | -1.89B | -1.88B | -2.03B | 218.05M | -1.90B | -532.23M |
| Net Income | -1.93B | -1.93B | -2.02B | 168.35M | -1.95B | -582.45M |
Balance Sheet | ||||||
| Total Assets | 7.52B | 7.52B | 9.08B | 10.71B | 9.60B | 10.91B |
| Cash, Cash Equivalents and Short-Term Investments | 6.99B | 6.99B | 8.41B | 10.22B | 8.88B | 10.17B |
| Total Debt | 0.00 | 0.00 | 0.00 | 531.00K | 3.67M | 9.73M |
| Total Liabilities | 204.43M | 204.43M | 185.88M | 336.02M | 192.43M | 212.64M |
| Stockholders Equity | 7.31B | 7.31B | 8.89B | 10.37B | 9.40B | 10.70B |
Cash Flow | ||||||
| Free Cash Flow | 0.00 | -1.46B | -1.88B | 1.13B | -1.40B | -609.23M |
| Operating Cash Flow | 0.00 | -1.41B | -1.88B | 1.14B | -1.40B | -519.65M |
| Investing Cash Flow | 0.00 | -42.50M | -4.78M | -344.00K | -330.00K | -92.72M |
| Financing Cash Flow | 0.00 | 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 |
|---|---|---|---|---|---|---|---|
56 Neutral | ¥8.54B | 42.69 | ― | ― | 2.99% | -52.75% | |
54 Neutral | ¥22.01B | -54.84 | ― | ― | -5.65% | -469.19% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | ¥14.12B | -50.65 | ― | ― | 1.24% | -33.41% | |
47 Neutral | ¥10.06B | -9.53 | ― | ― | -42.49% | -2.37% | |
46 Neutral | ¥20.27B | 561.01 | ― | ― | -32.68% | ― | |
43 Neutral | ¥17.49B | -9.14 | ― | ― | ― | 11.34% |
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.
StemRIM Inc. has announced the upcoming registration of a medical use patent for Redasemtide, its flagship regeneration-inducing drug candidate, specifically for treating fatty liver and non-alcoholic steatohepatitis (NASH) in Japan. With no existing drug treatments for these rising lifestyle-related conditions, this move could position StemRIM as a leader in addressing unmet medical needs while bolstering its market reputation within regenerative medicine.
StemRIM Inc. reported its financial results for the three months ending October 31, 2025, showing a net loss, with no operating revenue recorded. The company continues to focus on the development of its regenerative medicine products, including Redasemtide, and anticipates significant cash outflows for research and development. Despite the financial challenges, StemRIM has secured sufficient funds for its R&D activities through 2028, indicating a strong commitment to its long-term development goals.
StemRIM Inc. has completed the issuance of new shares as restricted stock compensation, totaling 545,000 shares at an issue price of 278 yen per share, amounting to 151,510,000 yen. This strategic move is expected to enhance the company’s operational capabilities and strengthen its position in the biotech industry, potentially benefiting stakeholders by advancing its innovative regenerative medicine products.
StemRIM Inc. has announced the establishment of a voluntary Compensation Committee to enhance transparency and effectiveness in determining the compensation of its directors and executive officers. This move is expected to provide an objective perspective on compensation matters, thereby strengthening the company’s governance structure and potentially improving stakeholder confidence.
StemRIM Inc. has announced its business plan centered around ‘Regeneration-Inducing Medicine,’ which promises to revolutionize the treatment of refractory diseases by harnessing the body’s innate tissue repair capabilities. This development could significantly impact the biotech industry by offering new therapeutic options and improving patient outcomes globally.
StemRIM Inc. has announced the issuance of new shares as remuneration for restricted stock, amounting to 545,000 ordinary shares at 278 yen per share, totaling 151,510,000 yen. This move is part of a Restricted Stock Grant System aimed at enhancing the company’s long-term corporate value and aligning the interests of its directors and auditors with shareholders by sharing both the benefits and risks of stock price fluctuations.
StemRIM Inc. has announced the patent registration for its stem cell gene therapy technology, SR-GT1, aimed at treating dystrophic epidermolysis bullosa, a genetic skin disorder. This innovative approach involves modifying mesenchymal stem cells to produce type VII collagen, potentially offering a curative treatment. While the financial impact for the fiscal year ending July 31, 2026, is minimal, the company is preparing for clinical trials, marking a significant step in regenerative medicine.