Price history
¥362Latest+6.8%
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Business overview
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Key numbersShowing 8 of 18
PER
11.18How many years of earnings it would take to buy the stock. The market average is generally considered to be around 15.PBR
6.84How many times the company's net assets? Around 1x is generally considered a benchmark.ROE
61.1%Earning power. A figure above 10% is generally considered good.Dividend yield
0.0%The annual dividend as a percentage of the share price.Market capitalization
¥46bnShare price × number of shares. The value of the entire company.Equity ratio
66.7%The proportion of assets funded by money that does not have to be repaid.Operating margin
12.3%The percentage of revenue remaining from the company’s core business.Revenue growth (3 years)
67.6%The average annual growth in sales over the past three years.What to watch next
Further progress in the regional sales expansion and indication expansion of core products, including TDM-621/PuraStat and TDM-644/PuraLift, including developments involving regulators, insurance coverage and reimbursement
Impact HighLikelihood Medium
Progress in the European marketing authorization application process for the next-generation hemostatic material TDM-623, including approval, non-approval or conditions
Medium term, within the typical range from application to approvalImpact HighLikelihood Low
Development milestones for the novel peptide hemostatic material identified in 2026 as a potential future core product, including concrete details regarding clinical trials and marketing authorization applications
Impact MediumLikelihood Medium
Clarification of updates to and continuation of the European sales structure, including FUJIFILM Europe's exclusive distribution rights, and the terms of the distribution agreement
Depending on the timing of the contract renewalImpact MediumLikelihood Medium
The pace of dilution from capital measures such as convertible bonds and stock acquisition rights, and the stability of funding, including the operation of commitment lines
Impact HighLikelihood High
What to watch next
Who owns itTop holders total 11.2%
Listed holders 11.2%Everyone else 88.8%
J.P. Morgan Securities Japan Co., Ltd.2.02%
BNY GCM CLIENT ACCOUNT JPRD AC ISG (UK)1.76%
Nagano Keiji (永野 恵嗣)1.45%
楽天証券株式会社1.26%
松本 松二1.09%
山田 祥美0.81%
Nomura Securities Co., Ltd.0.79%
Ishii Yoshiaki (石井 良明)0.68%
2 other listed holders1.31%
| Holder | Ownership (%) |
|---|---|
| J.P. Morgan Securities Japan Co., Ltd. | 2.02 |
| BNY GCM CLIENT ACCOUNT JPRD AC ISG (UK) | 1.76 |
| Nagano Keiji (永野 恵嗣) | 1.45 |
| 楽天証券株式会社 | 1.26 |
| 松本 松二 | 1.09 |
| 山田 祥美 | 0.81 |
| Nomura Securities Co., Ltd. | 0.79 |
| Ishii Yoshiaki (石井 良明) | 0.68 |
| 2 other listed holders | 1.31 |
This company's documents
Filings
Timely disclosures
- 2026-10-22Notice Regarding Selection for Inclusion in the TOPIX Next-tier Index Constituents
- 2026-09-10Consolidated Financial Results for the First Quarter of the Fiscal Year Ending April 2027 (Japanese GAAP)
- 2026-07-30Business Plan and Growth Potential
- 2026-07-22Notice Regarding the Finalization of the Terms of the Stock Options (Share Acquisition Rights)
- 2026-07-21Notice Regarding the Issuance of Stock Options (Share Acquisition Rights)
- 2026-07-17Questions Regarding the Briefing on the Full-Year Financial Results for the Fiscal Year Ending April 2026 and the Medium-Term Management Plan
- 2026-07-01Notice of Convocation of the 2026 Annual General Meeting of Shareholders and Meeting Materials
- 2026-06-26Notice Regarding the Streamlining of Approvals for PureLift
16 more
- 2026-06-22Notice Regarding the Issuance of Stock Options (Share Acquisition Rights)
- 2026-06-22Policy on Responses to Large-Scale Purchases of Our Shares and Other Securities
- 2026-06-12(Correction) Partial correction to the "Summary of Financial Results for the Fiscal Year Ended April 2026 (Japanese GAAP) (Consolidated)"
- 2026-06-11Notice Regarding the Recognition of Extraordinary Income and Extraordinary Losses
- 2026-06-11Notice Regarding the Removal of the Going Concern Qualification
- 2026-06-11Financial Results for the Fiscal Year Ended April 2026 (Japanese GAAP) (Consolidated)
- 2026-06-08Notice of Completion of the Physician-Initiated Phase I Clinical Trial of “MIRX002” for Malignant Pleural Mesothelioma and Achievement of the Primary Endpoint
- 2026-06-05Notice Regarding Revisions to Earnings Forecasts
- 2026-05-29Notice Regarding the Resignation of a Director
- 2026-05-19Notice Regarding Revisions to Earnings Forecasts and Recognition of Non-operating Income
- 2026-03-12Notice Regarding the Recognition of Non-Operating Income and Extraordinary Loss
- 2026-03-12Notice Regarding Revisions to Earnings Forecasts
- 2026-03-12Earnings Summary for the Third Quarter of the Fiscal Year Ending April 2026 [Japanese GAAP] (Consolidated)
- 2026-03-06欧州における「PuraStat」の粘膜創傷治癒用途へのCEマーク変更申請のお知らせ
- 2026-02-25Notice Regarding a Change in Representative Director (Change of President)
- 2026-02-24第9回無担保転換社債型新株予約権付社債の転換完了について
Threads
- 2026-10-22TOPIX Next-tier選定を契機とする機関投資家との関係強化
- 2026-09-10Expanding the Pipeline Across Multiple Fields and Launching Products Early
- 2026-09-10A Business Model Complementing Manufacturing and Sales Through Partnerships
- 2026-09-10Expanding Overseas Sales Regions for TDM-621
- 2026-09-10Going-Concern Risk from Front-Loaded Research and Development Spending
- 2026-09-10Foreign-Exchange Risk from Foreign-Currency Transactions
- 2026-09-10Completion of Preclinical Studies and Clinical-Trial Protocol Development for Next-Generation Hemostat TDM-623
- 2026-09-10Annual Targets for Product Sales Revenue and Research and Development Expenses
71 more
- 2026-09-10Enhancing Product Value Through Expanded Indications and Functions for TDM-621
- 2026-09-10Developing a Radiation Proctitis Treatment Starting with an Oral Mucositis Healing Material
- 2026-09-10Achieving Profitability from the Fiscal Year Ending April 2023 Onward
- 2026-09-10Sustainability Policy and the Need to Establish Related Metrics
- 2026-09-10Planned formulation and publication of a new medium-term management plan
- 2026-09-10Development as a slow-release carrier for existing drugs
- 2026-07-30Uncertainty Surrounding Clinical Trials, Regulatory Approval, and Reimbursement Listing
- 2026-07-30Revenue Dependence on Specific Partners and Manufacturing Supply Risk
- 2026-07-22Medical Business Based on Self-Assembling Peptides
- 2026-07-22Risk of Delays in Overseas Sales Plans and Sales Partnerships
- 2026-07-22Acquiring Applied Technologies Through Joint Research with External Institutions
- 2026-07-22Securing Funding to Continue Research and Development
- 2026-07-22Dependence on a Small Organization, the Representative Director, and Specialized Personnel
- 2026-07-22Strengthening Management Controls to Support Global Expansion
- 2026-07-22Prioritizing Research and Development, with Dividends to Be Considered After Eliminating Accumulated Losses
- 2026-07-22Dilution of Share Value through the Exercise of Stock Acquisition Rights
- 2026-07-22Risk of Expiration of Tax Loss Carryforwards
- 2026-07-22Risk of Forecasting Performance Due to Limited Operating History and a Front-Loaded Investment Stage
- 2026-07-22Risk of Failing to Raise Expected Funds Due to Dependence on Stock Acquisition Right Exercises
- 2026-07-22Risk of Excess Inventory and Write-Downs from Missing Sales Targets
- 2026-07-22Minimizing Clinical Development Costs and Time Through Favorable Market Selection
- 2026-07-22Director Compensation Policy Including KPI-Linked and Share-Based Compensation
- 2026-07-22Reimbursement Listing for TDM-644 and Cross-Selling with Hemostatic Products
- 2026-07-22Japanese Reimbursement Coverage for TDM-621 and Accelerating Domestic Sales
- 2026-07-22U.S. Market Launch of TDM-621 Following FDA Approval
- 2026-07-22Negative Net Worth at Overseas Subsidiaries
- 2026-07-22Liquidity Risk from Breaches of Financial Covenants and Early Redemption Clauses
- 2026-07-22Lawsuit by a Former Employee Seeking Invalidity of Dismissal and Damages
- 2026-07-22Impairment of Operating Assets Due to Lower Profitability
- 2026-07-22Planned Adoption of Lease Accounting Standards from the Fiscal Year Ending April 2028
- 2026-07-22Planned Adoption in 2028 of Accounting Standards for Subsequent Events
- 2026-07-22Dissolution and Liquidation Proceedings for a Consolidated Subsidiary
- 2026-07-17Transparent, Sound Management and Proactive Disclosure
- 2026-07-17Strengthening Dedicated Marketing and Clinical Sales Support in Australia
- 2026-07-17Licensing the DDS Business to Major Pharmaceutical Companies
- 2026-07-17Introduction of a policy for responding to large-scale purchases and other transactions (takeover defense measure)
- 2026-07-17Consideration of future options for the listing market
- 2026-07-17Preclinical development of OKD-001, an A6K-based drug for BNCT
- 2026-06-11FDA Discussions and Candidate Selection for U.S. Commercialization of an Adhesion-Prevention Material
- 2025-12-11Separate Presentation of U.S. Revenue
- 2025-07-24Next Phase of U.S. Clinical Development for the Alveolar Bone Regeneration Material TDM-711
- 2025-07-24Investigator-Initiated Trial of TDM-812 Using A6K
- 2025-07-24Risk to Australian Sales Prices and Earnings from Private Insurance Pricing Revisions
- 2025-07-24Promoting Workforce Diversity, Development, and Flexible Working Arrangements
- 2025-07-24Risk of Losses from Remittance Fraud
- 2025-07-24Administrative Sanctions Against the Audit Firm and Auditor Reappointment
- 2025-07-24Risk of Cyberattacks, Information Leaks, and System Failures
- 2025-07-24Domestic Animal Studies of an Absorbable Tissue Spacer for Radiation Therapy
- 2024-12-12Participation in COVID-19 Antibody Test Kit and Vaccine-Related Projects
- 2024-07-25Protection of Core Patents, Competition, and Third-Party Rights Risk
- 2024-07-25Revenue Dependence on Absorbable Local Hemostat Products
- 2024-07-25Risk of Disruptions to Sales and Clinical Activities Due to COVID-19
- 2024-03-13Repeat Clinical Trial and Regulatory Approval for TDM-621 in Japan
- 2024-03-13Expanding Approved Uses of the Wound-Healing Material TDM-511
- 2024-03-13MIT-Derived Patent Licensing Platform for Self-Assembling Peptides
- 2024-03-13Additional CE-Mark Uses and European Certification for a Postoperative Bleeding-Prevention Material
- 2024-03-13Reducing Product Cost Ratios Through Changes in Sterilization Methods and Manufacturing Scale-Up
- 2024-03-13Management of the medical products business, including the antibody testing kit business, as a single segment
- 2023-03-17Completion of Liquidation and Removal from Consolidation of a Latin American Subsidiary
- 2022-12-13Appointment of a provisional corporate auditor following a vacancy among outside auditors
- 2022-07-28Product Liability and Reputational Risk for Medical Products
- 2022-07-28Adoption of the Accounting Standard for Fair Value Measurement
- 2022-07-28Managing executive liability through directors and officers liability insurance
- 2022-03-15Building an Applied Research Ecosystem Through Research Reagent Sales
- 2021-09-14Uncertainty Over the Efficacy and Product Advantages of TDM-641
- 2021-09-14Launch of U.S. Clinical Trials for TDM-621
- 2021-09-14Earnings Volatility Due to the Timing of Upfront Payments and Milestone Revenue
- 2021-09-14Adoption of Revenue Recognition Accounting Standards
- 2021-07-30Preclinical and Animal-Model Studies of the Vascular Embolization Material TDM-631
- 2021-07-30Risk of Failing to Achieve the Expected Returns on Raised Capital
- 2021-03-16Web-Based Sales and Marketing Activities During the COVID-19 Era