Contents of this document
- Capital and business alliance with 千寿製薬 and an option agreement covering Japan, Asia and other markets for H-1337
- Basic agreement with U.S. company Terrain on a sales partnership for DW-5LBT
- License agreement with Keio University for H-1129
- Joint research with LABバイオテック社 on therapeutics for eye diseases using lactic acid bacterium-derived EVs
- A shift in policy to prioritize development of H-1337 in Japan over the United States
- Cumulative performance of marketed products4 Products
- Late-stage development products (Phase 3 or later)5 Instrument
- Number of kinase inhibitors in the compound library1,500 Approx. number
- Out-licensing track record7 Instrument
- U.S. lidocaine patch market295 US$ million 2025
- Lidoderm generic product shareApprox. 90% by volume and approx. 60% by value
- Number of patients with Fuchs endothelial corneal dystrophy in Europe16 Approx. million people
- Number of patients with Fuchs endothelial corneal dystrophy in the United States6 Approx. million people
| Item | Details |
|---|---|
| Document type | Financial results presentation |
| Fiscal Period Covered | Second quarter of the fiscal year ending December 2026 |
| Net Sales | ¥33 million (YoY -80.9%) |
| Operating profit | ¥-312 million |
| Ordinary income | ¥-322 million |
| Net income | ¥-323 million |
| Selling, general and administrative expenses | ¥346 million |
| Full-year earnings forecast | Net Sales ¥300 million / Operating loss ¥-780 million / Ordinary loss ¥-800 million / Net loss attributable to owners of the parent ¥-800 million / Research and development costs ¥780 million |
| Progress against full-year forecast | Net Sales 11.0% / Research and development costs 27.9% / Proceeds from the 13th stock acquisition rights 90.9% |
| Self-assessment against the plan | Research and development expenses are broadly in line with the plan |
| Breakdown of Factors Affecting the Change | Net Sales Lower royalties due to the expiration of patents for DW-1002 outside the United States; U.S. royalties for January through June are scheduled to be recorded as a lump sum when the agreement is executed |
| Key KPIs | Indicator name Cumulative performance of marketed products / Value 4 Products / Year on year against the same period last year Not disclosed, Indicator name Late-stage development products (Phase 3 or later) / Value 5 Instrument / Year on year against the same period last year Not disclosed, Indicator name Number of kinase inhibitors in the compound library / Value 1,500 Approx. number / Year on year against the same period last year Not disclosed, Indicator name Out-licensing track record / Value 7 Instrument / Year on year against the same period last year Not disclosed |
| Number of employees | Number of Employees 29 People (consolidated) / Change during the period Not disclosed / Hiring plan Not disclosed |
| Capital expenditures | ¥6 millions (purchases of property, plant and equipment) |
| Market Size / Share | Market U.S. lidocaine patch market / Value 295 US$ million (2025), Market Lidoderm generic product share / Value Approx. 90% by volume and approx. 60% by value, Market Number of patients with Fuchs endothelial corneal dystrophy in Europe / Value 16 Approx. million people, Market Number of patients with Fuchs endothelial corneal dystrophy in the United States / Value 6 Approx. million people |
| New initiatives | Capital and business alliance with 千寿製薬 and an option agreement covering Japan, Asia and other markets for H-1337, Basic agreement with U.S. company Terrain on a sales partnership for DW-5LBT, License agreement with Keio University for H-1129, Joint research with LABバイオテック社 on therapeutics for eye diseases using lactic acid bacterium-derived EVs, A shift in policy to prioritize development of H-1337 in Japan over the United States |
Items this document does not state (15)
These are items the company does not state in this document. We do not leave them blank, nor fill them in from other sources or by inference.
The reasons the company gives
The company's own explanation, not something inferred from the numbers.The decrease in revenue was due to lower royalties following the expiration of patents for DW-1002 outside the United States, while royalties for the United States are scheduled to be recorded as a lump sum when the agreement is executed. The decrease in revenue appears to be the main factor behind the operating loss, but the materials do not explicitly identify the factors contributing to the operating loss.