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HUTCHMED (China) (HCM) investor relations material
HUTCHMED (China) H1 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Net income reached $455 million in H1 2025, mainly from a $609 million gain on partial SHPL divestment, with cash and short-term investments at $1.36 billion as of June 30, 2025.
Global commercial success for Zecla/FRUZAQLAⓇ, with 25% year-over-year growth and launches in over 30 countries.
Oncology/Immunology revenue declined 15% year-over-year to $143.5 million, with total revenue down 9–10% to $277.7–$278 million.
Advanced late-stage pipeline and ATTC platform, with first clinical trial initiation expected by late 2025.
Key product approvals and launches included new indications for savolitinib/ORPATHYSⓇ, fruquintinib/ELUNATEⓇ, and TAZVERIKⓇ in China.
Financial highlights
Net income attributable to shareholders was $455 million for H1 2025, up from $25.8 million in H1 2024, driven by the SHPL divestment gain.
Total revenue for H1 2025 was $277.7–$278 million, down 9–10% year-over-year; Oncology/Immunology revenue was $143.5 million, down 15%.
R&D investments totaled $72 million, with operating expenses and S&A costs reduced year-over-year.
Cash and short-term investments increased to $1.36 billion, with net cash inflows of $519.1 million (non-GAAP).
EPS rose to $0.53 per share ($2.65 per ADS) from $0.03 per share ($0.15 per ADS) in H1 2024.
Outlook and guidance
Full-year 2025 Oncology/Immunology revenue guidance revised to $270–$350 million due to milestone phasing and regulatory review delays.
Anticipate improved sales growth in H2 2025, supported by new approvals and expanded reimbursement.
Multiple NDA submissions and clinical trial readouts expected in the next 12 months.
Strong cash position will be leveraged for ATTC global development and acquisitions.
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