Deutsche Bank’s Depositary Receipts Virtual Investor Conference
Logotype for HUTCHMED (China) Limited

HUTCHMED (China) (HCM) Deutsche Bank’s Depositary Receipts Virtual Investor Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for HUTCHMED (China) Limited

Deutsche Bank’s Depositary Receipts Virtual Investor Conference summary

20 Jan, 2026

Key product launches and commercial performance

  • Fruquintinib (FRUZAQLA) achieved $130 million in sales in H1, with recent approvals in the U.S., Europe, UK, and Japan, and strong market share in China exceeding 40%.

  • SULANDA maintains a solid second position in China's neuroendocrine tumor market, benefiting from insurance inclusion and broad patient access.

  • Savolitinib, a MET inhibitor for lung cancer, generated $25 million in H1 sales in China and is awaiting pivotal trial data for potential U.S. and global expansion.

  • Sovleplenib, targeting immune thrombocytopenia, is filed for approval in China with launch expected in 2025, and shows a 48% durable response rate in late-line patients.

Pipeline development and clinical milestones

  • Fruquintinib is being developed for additional indications, including endometrial and renal cell carcinoma, with regulatory filings and data readouts expected by early next year.

  • Savolitinib's SAVANNAH trial for second-line lung cancer is expected to report data by year-end, with potential U.S. FDA filing soon after.

  • Sovleplenib is also in phase III for warm AIHA, a rare autoimmune anemia with no approved therapies, and may become the first global treatment.

  • Additional late-stage assets include HMPL-453 for intrahepatic carcinoma and HMPL-306 for AML, both advancing in registration trials.

Competitive positioning and innovation

  • Fruquintinib demonstrates superior efficacy and lower toxicity compared to competitors, driving rapid adoption and inclusion in clinical guidelines.

  • Savolitinib is differentiated as a MET-specific therapy, free from chemotherapy, and offers oral administration, targeting a $1 billion market in China and globally.

  • Sovleplenib addresses significant unmet needs in ITP and warm AIHA, with a favorable safety profile and potential to expand the treatable patient population.

  • The company emphasizes rigorous preclinical selection, high molecular selectivity, and a robust chemistry team to ensure low off-target toxicity.

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