SanBio Company (4592) Q3 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2025 earnings summary
3 Oct, 2025Executive summary
Achieved regulatory approval in Japan for AKUUGO®, a cell therapy for chronic motor paralysis from traumatic brain injury, with shipment delayed to Q2 FY2026 due to manufacturing compliance issues.
Focus remains on global expansion, especially the US, and new clinical trials for chronic ischemic stroke are planned.
Financial highlights
Operating loss for the nine months ended October 31, 2024 was ¥2,482 million, an improvement from ¥3,725 million year-over-year.
Net loss attributable to owners of parent was ¥2,152 million, compared to ¥1,883 million in the prior year.
Research and development expenses totaled ¥1,666 million, mainly for SB623 program manufacturing.
Foreign exchange gains of ¥499 million were recorded as non-operating income.
Comprehensive loss for the period was ¥2,675 million.
Outlook and guidance
No revision to the full-year forecast; projected net loss for FY2025 is ¥3,359 million, with no dividend planned.
Earnings forecasts are based on current information and may vary due to various factors.
Latest events from SanBio Company
- AKUUGO® approved in Japan, fueling R&D and expansion, but losses expected to deepen.4592
Q4 202625 Mar 2026 - Net loss widened to ¥2,713 million; major funding secured for AKUUGO® and clinical trials.4592
Q3 202615 Dec 2025 - Akugo/AKUUGO® gains conditional approval in Japan as losses narrow and global expansion advances.4592
Q2 20253 Oct 2025 - Losses widened on higher R&D and FX losses; financing secured, AKUUGO® approval expected.4592
Q2 20263 Oct 2025 - AKUUGO® approved in Japan; global expansion and clinical trials continue amid high R&D costs.4592
Q4 20253 Oct 2025 - Net loss improved, regulatory decision on SB623 expected in June, no dividend planned.4592
Q1 20253 Oct 2025 - Q1 net loss deepened to ¥1,531 million as AKUUGO® nears launch and new funding is secured.4592
Q1 20263 Oct 2025