公司資料

HUTCHMED 股價、新聞與催化劑

股票代碼:
HCM
交易所:
NASDAQ
產業:
Biopharma
所在地:
China and listed in the U

股票表現

12.56 USD (+2.95%)

收盤價

最後更新: 2026年8月17日

1.98B USD

市值

股價為何變動

Following the latest company update, “HUTCHMED Announces ORPATHYS® Plus TAGRISSO® Demonstrated Statistically Significant and Clinically Meaningful Improvements in Progression-Free and Overall Survival in MET-Driven EG…”, HCM closed up 2.95% at $12.56 on Aug 17, 2026. The move occurred in the trading session associated with this clinical readout update.

公司概覽

China-Originated Oncology Company

HUTCHMED is an oncology-focused biopharmaceutical company with commercial products in China and partnered global products. Its strategy combines China commercialization, global partnerships, and internal R&D aimed at differentiated small molecules and newer antibody-targeted modalities.

Commercial Oncology Portfolio

The company's commercial base includes ELUNATE, SULANDA, FRUZAQLA, ORPATHYS, and other oncology products. First-half 2026 growth was led by a rebound in China product sales and geographic expansion of FRUZAQLA outside China, which had approvals or launches in 41 countries.

Late-Stage Regulatory Pipeline

HUTCHMED has multiple late-stage programs across oncology and immunology. Recent progress includes China approval of ELUNATE with sintilimab for second-line kidney cancer, China NDA acceptances for sovleplenib in wAIHA and ITP, ORPATHYS approval in third-line MET-amplified gastric cancer, and positive data for fanregratinib in FGFR2 fusion or rearrangement intrahepatic cholangiocarcinoma.

ATTC Innovation Strategy

The company is investing in antibody-targeted therapy conjugates, or ATTCs, that use antibody targeting to deliver potent small-molecule payloads to tumor cells. HMPL-A251, HMPL-A580, and HMPL-A830 represent a newer platform layer intended to create first-in-class or best-in-class candidates and support multinational partnering opportunities.

未來催化劑

  • Topline results from SAFFRON and SANOVO Phase 3 savolitinib studies in the second half of 2026.
  • NMPA review of sovleplenib in wAIHA and ITP.
  • Global clinical trial initiation for HMPL-A830 in the second half of 2026.

近期新聞

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