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CANbridge Pharmaceuticals (1228) investor relations material
CANbridge Pharmaceuticals H1 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Achieved key milestones in rare disease drug pipeline, including new product approvals, expanded insurance coverage in China, and strategic cooperation with Baheal Medical, securing RMB50 million engagement fee and HK$100 million equity investment.
Three rare disease products passed China's NHSA innovative drug catalog review, supporting future reimbursement and market access.
Streamlined operations, reduced workforce to 45, and prioritized key rare disease programs amid challenging biotech funding environment.
Commercial launches of Hunterase® and Livmarli® accelerated patient identification and insurance coverage.
Gaurunning® received marketing approval for Gaucher disease in China, marking a significant product milestone.
Financial highlights
Revenue dropped 50.3% year-over-year to RMB22.2 million, mainly due to cessation of Nerlynx® sales in Taiwan; excluding this, revenue declined 6.9%.
Gross profit was RMB15.4 million with a margin of 69.3%, up from 65.7% last year.
Other income and gains surged to RMB104.1 million, driven by a RMB101.0 million gain from US lease termination.
R&D expenses fell 89.6% to RMB18.0 million after Gaurunning NDA approval; admin and selling expenses also decreased significantly.
Reported profit of RMB59.2 million (vs. RMB247.3 million loss prior year), mainly from non-recurring items; adjusted loss narrowed to RMB37.4 million.
Cash and bank balances at RMB2.0 million, with net current liabilities of RMB462.7 million and net liabilities of RMB409.1 million as of June 30, 2025.
Outlook and guidance
Optimistic for H2 2025, focusing on pipeline streamlining, capital efficiency, and leveraging Baheal Medical partnership for growth.
Plans to accelerate commercialization of Gaurunning and improve profitability of Hunterase® and Livmarli®.
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