Contents of this document
- Transform the entire R&D organization into a global, end-to-end structure
- Invest in AI-enabled protein design, AI-driven gene therapy and Human-in-the-Loop platforms
- Use Evinova's AI-native Study Designer platform
- Automate cell therapy manufacturing through the Mahol-A-Ba robotics platform
- Insourcing clinical operations
- Strategic partnership with Vir Biotechnology for the development and commercialization of VIR-5500 (before completion of the transaction)
- Number of patients treated with Astellas products174 million patients
- Number of countries where products are availableMore than 100 countries
- Reduction in the time from IND acceptance to activation of the first clinical trial site69%Year on year against the same period last yearFY24/FY25 vs. FY23
- Reduction in the time from IND acceptance to first patient dosing67%Year on year against the same period last yearFY24/FY25 vs. FY23
- Median time from receipt of topline results to filing115 days
- Reduction in the timeline to filing14%Year on year against the same period last yearFY25 vs. FY23
- Number of approvals obtained for priority strategic products in key regions8 items
- TargetAdvance 10 new active ingredients to the Phase III stageTarget fiscal yearThrough 2034
- TargetRaise R&D productivity to a top-tier industry levelTarget fiscal year2030-2034
| Item | Details |
|---|---|
| Document type | Medium-Term Management Plan Presentation |
| Key KPIs | Indicator name Number of patients treated with Astellas products / Value 174 million patients / Year on year against the same period last year Not disclosed, Indicator name Number of countries where products are available / Value More than 100 countries / Year on year against the same period last year Not disclosed, Indicator name Reduction in the time from IND acceptance to activation of the first clinical trial site / Value 69% / Year on year against the same period last year FY24/FY25 vs. FY23, Indicator name Reduction in the time from IND acceptance to first patient dosing / Value 67% / Year on year against the same period last year FY24/FY25 vs. FY23, Indicator name Median time from receipt of topline results to filing / Value 115 days / Year on year against the same period last year Not disclosed, Indicator name Reduction in the timeline to filing / Value 14% / Year on year against the same period last year FY25 vs. FY23, Indicator name Number of approvals obtained for priority strategic products in key regions / Value 8 items / Year on year against the same period last year Not disclosed |
| Medium-term management plan targets | Target Advance 10 new active ingredients to the Phase III stage / Target fiscal year Through 2034, Target Raise R&D productivity to a top-tier industry level / Target fiscal year 2030-2034 |
| New initiatives | Transform the entire R&D organization into a global, end-to-end structure, Invest in AI-enabled protein design, AI-driven gene therapy and Human-in-the-Loop platforms, Use Evinova's AI-native Study Designer platform, Automate cell therapy manufacturing through the Mahol-A-Ba robotics platform, Insourcing clinical operations, Strategic partnership with Vir Biotechnology for the development and commercialization of VIR-5500 (before completion of the transaction) |
Items this document does not state (27)
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.To accelerate the delivery of value to patients, improve R&D productivity and efficiency, and shift to a long-term growth trajectory after the expiration of XTANDI's exclusivity period. The company said it would concentrate on higher-value programs, strengthen clinical trial execution capabilities and invest in capabilities such as AI.