Contents of this document
- A new drug application was filed in Japan for olutasidenib for the indication of relapsed or refractory acute myeloid leukemia with an IDH1 gene mutation.
- Development and commercialization rights for olutasidenib in Taiwan were licensed to Orient EuroPharma Co., Ltd.
- 台田薬品股份有限公司, the sublicensee in Taiwan, filed an application for approval of fostamatinib.
- The Japanese package insert for Tavneos was revised, and a safety alert was issued.
| Item | Details |
|---|---|
| Document type | Supplementary materials to the earnings report |
| Fiscal Period Covered | First quarter of the fiscal year ending March 2027 |
| Net Sales | ¥23,389 million (YoY +5.4%) |
| Operating profit | ¥1,095 million (YoY -48.0%) |
| Ordinary income | ¥2,185 million (YoY -25.0%) |
| Net income | ¥4,723 million (YoY +4.5%) |
| Selling, general and administrative expenses | ¥10,337 million |
| Results for the three months of the current quarter | The results for the first quarter of the fiscal year ending March 2027 were: net sales of ¥23,389 million, operating income of ¥1,095 million, ordinary income of ¥2,185 million, and quarterly net income attributable to owners of the parent of ¥4,723 million. |
| Full-year earnings forecast | Net Sales ¥88,700 million / Operating profit ¥2,000 million / Ordinary income ¥4,000 million / Profit attributable to owners of the parent ¥13,300 million / Cost of sales ¥46,600 million / Selling, general and administrative expenses ¥40,100 million / Research and development costs ¥14,300 million |
| Segment results | Pharmaceuticals Business Sales ¥19,464 million / yoy_pct 4.2 / Information Services Business Sales ¥3,074 million / yoy_pct 34.8 / Construction and Facility Maintenance Sales ¥607 million / yoy_pct -38.8 / Product sales business Sales ¥243 million / yoy_pct 2.7 |
| Breakdown of Factors Affecting the Change | Net sales were driven by growth in Ixelti, Beova, CORSUVA and Tavalisse, among other factors. Operating income and ordinary income were affected by the higher cost of sales ratio and an increase in selling, general and administrative expenses, mainly research and development expenses. Net income was affected by the recognition of gains on the sale of investment securities. A bridge showing the change by factor is Not disclosed. |
| New initiatives | A new drug application was filed in Japan for olutasidenib for the indication of relapsed or refractory acute myeloid leukemia with an IDH1 gene mutation., Development and commercialization rights for olutasidenib in Taiwan were licensed to Orient EuroPharma Co., Ltd., 台田薬品股份有限公司, the sublicensee in Taiwan, filed an application for approval of fostamatinib., The Japanese package insert for Tavneos was revised, and a safety alert was issued. |
Items this document does not state (19)
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.Revenue from the pharmaceuticals business increased, driven by growth in Ixelti, Beova, CORSUVA and Tavalisse, which were launched in March 2026, among other factors. In terms of profit, operating income and ordinary income decreased due to a higher cost of sales ratio and an increase in selling, general and administrative expenses, mainly research and development expenses. Meanwhile, quarterly net income attributable to owners of the parent increased due to the recognition of gains on the sale of investment securities.