Jiangsu Recbio Technology (2179) H1 2025 earnings summary
Event summary combining transcript, slides, and related documents.
H1 2025 earnings summary
15 Oct, 2026Executive summary
H1 revenue reached RMB10.9m, mainly from licensing, while net loss widened to RMB340.7m from RMB249.6m as R&D spending rose.
REC603 and REC610 remained in Phase III; REC610 completed enrollment and full-course vaccination of 24,640 participants, while REC603 began month-48 follow-up.
Biological E’s REC603 licensing agreement generated an upfront payment, with further milestone payments and sales-based royalties.
Financial highlights
Revenue was RMB10.9m versus nil in H1 2024, mainly from intellectual-property licensing; gross profit was RMB67k.
Net loss was RMB340.7m versus RMB249.6m; basic and diluted loss per share widened to RMB0.71 from RMB0.52.
R&D costs rose 46.0% to RMB299.6m; other income and gains fell 66.1% to RMB12.1m, while administrative expenses declined 12.6% to RMB47.8m.
Finance costs rose 40.7% to RMB12.8m, mainly due to additional debt financing; selling and distribution expenses fell 46.7% to RMB0.8m.
Operating cash outflow was RMB224.0m versus RMB279.9m.
Outlook and guidance
REC603 month-48 follow-up continues; interim analysis using pathological endpoints is planned, with BLA submission anticipated in 2026 subject to conditions.
REC610 follow-up continues; targets include a clinical analysis report by Sep 2025, BLA submission by Dec 2025 and approval by Nov 2026, subject to outside dates.
REC625 preclinical studies are planned for completion in 2025; further REC604c development depends on market demand and available resources.
Priorities include accelerating clinical development and commercialization of HPV and shingles vaccines, strengthening R&D and manufacturing, and expanding international business development.
Latest events from Jiangsu Recbio Technology
- H1 losses narrowed as R&D spending fell, while cash burn rose and vaccine programs advanced.2179
H1 2023 - Nil revenue, RMB572.4m net loss, and a Phase III-to-commercialization pipeline.2179
H2 2023 - REC603 advanced toward a conditional 2025 BLA target as cash tightened and leverage rose.2179
H1 2024 - Phase III vaccine progress continued as losses persisted and liquidity tightened.2179
H2 2024 - REC610 entered marketing review as losses widened and capital shifted toward core vaccine programs.2179
H2 2025 - Loss narrowed as REC610 advanced, but liquidity tightened and REC603 remained in Phase III.2179
H1 2026