Contents of this document
- Development of a new extended-release granule formulation for KP2011 and the expected start of a Phase 3 trial during fiscal 2026
- Establishment of a commercial-scale manufacturing and supply system for clinical trial cells through collaboration with a CDMO for KP8011
- Selection for an AMED public call for proposals, participation as a partner company, and consideration of launching multiple new development pipelines
- Partnership negotiations with domestic and overseas pharmaceutical companies for KP8011, KP2011 overseas, KP2021 and KP2032, among others
- ALS—North America¥825 billionNumber of patients33,000 patients
- ALS—Europe¥120 billionNumber of patients24,000 patients
- ALS—China¥100 billionNumber of patients20,000 people
- ALS—India¥255 billionNumber of patients51,000 patients
- ALS—Japan¥25 billionNumber of patients10,000 people
- HD—North America¥315 billionNumber of patients33,000 patients
- FTD—Japan¥30 billionNumber of patients12,000 patients
- Hearing loss—Japan¥6 trillionNumber of patients12 million patients
- Alzheimer’s disease—Japan¥8 trillionNumber of patients4 million
- Subacute spinal cord injury—Japan¥250 billionNumber of patients5,000 patients per year
- Chronic spinal cord injury—Japan¥7.5 trillionNumber of patients150,000 passengers
- Ischemic stroke—Japan¥65 trillionNumber of patients1.3 million patients
- Chronic traumatic brain injury—Japan¥2.84 trillionNumber of patients56,800 patients
- Chronic cerebral hemorrhage—Japan¥10 trillionNumber of patients200,000 patients
| Item | Details |
|---|---|
| Document type | Financial Results Presentation |
| Fiscal Period Covered | Second quarter (interim period) of the fiscal year ending December 2026 |
| Net Sales | 0 Millions of yen |
| Operating profit | ¥-471 million (operating loss) |
| Net income | ¥-492 millions (interim net loss) |
| Selling, general and administrative expenses | 471 Millions of yen |
| Self-assessment against the plan | Progressing as planned |
| Number of employees | Number of Employees 21 People / As of As of 30 June 2026 / Changes during the period and hiring plan Not disclosed |
| Market Size / Share | Subject ALS—North America / Market Size ¥825 billion / Number of patients 33,000 patients, Subject ALS—Europe / Market Size ¥120 billion / Number of patients 24,000 patients, Subject ALS—China / Market Size ¥100 billion / Number of patients 20,000 people, Subject ALS—India / Market Size ¥255 billion / Number of patients 51,000 patients, Subject ALS—Japan / Market Size ¥25 billion / Number of patients 10,000 people, Subject HD—North America / Market Size ¥315 billion / Number of patients 33,000 patients, Subject FTD—Japan / Market Size ¥30 billion / Number of patients 12,000 patients, Subject Hearing loss—Japan / Market Size ¥6 trillion / Number of patients 12 million patients, Subject Alzheimer’s disease—Japan / Market Size ¥8 trillion / Number of patients 4 million, Subject Subacute spinal cord injury—Japan / Market Size ¥250 billion / Number of patients 5,000 patients per year, Subject Chronic spinal cord injury—Japan / Market Size ¥7.5 trillion / Number of patients 150,000 passengers, Subject Ischemic stroke—Japan / Market Size ¥65 trillion / Number of patients 1.3 million patients, Subject Chronic traumatic brain injury—Japan / Market Size ¥2.84 trillion / Number of patients 56,800 patients, Subject Chronic cerebral hemorrhage—Japan / Market Size ¥10 trillion / Number of patients 200,000 patients |
| New initiatives | Development of a new extended-release granule formulation for KP2011 and the expected start of a Phase 3 trial during fiscal 2026, Establishment of a commercial-scale manufacturing and supply system for clinical trial cells through collaboration with a CDMO for KP8011, Selection for an AMED public call for proposals, participation as a partner company, and consideration of launching multiple new development pipelines, Partnership negotiations with domestic and overseas pharmaceutical companies for KP8011, KP2011 overseas, KP2021 and KP2032, among others |
Items this document does not state (21)
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 company explained that, while each development pipeline was progressing generally as planned, selling, general and administrative expenses were lower than initially expected for the period. It also stated that cash and deposits decreased due to spending on research and development, personnel expenses and other working capital.