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HUTCHMED

18.420

+0.3702.05%

Volume:6.17M

Turnover:114.09M

Market Cap:16.06B

PE:4.52

High:18.880

Open:17.840

Low:17.840

Close:18.050

52wk High:30.750

52wk Low:15.570

Shares:872.00M

HK Float Shares:872.00M

Volume Ratio:1.34

T/O Rate:0.71%

Dividend:- -

Dividend Rate:- -

EPS(LYR):4.078

ROE:45.25%

ROA:-1.62%

PB:1.65

PE(LYR):4.52

PS:3.73

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Overview Company News Filings

HUTCHMED to Unveil Data at ASCO 2026 Annual Meeting

HUTCHMED to Showcase Positive Savolitinib Phase II Results and Broad Fruquintinib/Surufatinib Analyses at 2026 ASCO

Bulletin Express

HUTCHMED says savolitinib Phase II gastric cancer study posts 32.3% response rate

HUTCHMED Highlights Clinical Data to be Presented at the 2026 ASCO Annual Meeting

HUTCHMED, Innovent obtain NMPA clearance for ELUNATE-TYVYT regimen in second-line renal cell carcinoma

Bulletin Express

HUTCHMED gains NMPA green light for ELUNATE® + TYVYT® combo in second-line renal cell carcinoma; Innovent secures 10th sintilimab indication

Bulletin Express

HUTCHMED and Innovent Jointly Announce Nmpa Approval for Elunate® (Fruquintinib) in Combination With Tyvyt® (Sintilimab Injection) for the Treatment of Patients With Locally Advanced or Metastatic Renal Cell Carcinoma

THOMSON REUTERS

HUTCHMED Announces Updated Board Composition and Committee Assignments

Bulletin Express

HUTCHMED files directors list with Hong Kong Stock Exchange

HUTCHMED gains 99%-plus shareholder support for all AGM motions, green-lights 2026 Share Option Scheme

Bulletin Express

HUTCHMED China Ltd - Announcement on Results of Annual General Meeting

THOMSON REUTERS

HUTCHMED (China) Ltd - Nda for Sovlepenib for Waiha Accepted and Granted Priority Review by China Nmpa

THOMSON REUTERS

HUTCHMED (China) Ltd - Announces Nda Acceptance in China With Priority Review and Breakthrough Designation for Sovlepenib

THOMSON REUTERS

HUTCHMED Gets NMPA Priority Review for Sovleplenib NDA Targeting Warm Autoimmune Hemolytic Anemia

Bulletin Express

HUTCHMED's Sovleplenib NDA for Warm Autoimmune Hemolytic Anemia Accepted in China with Priority Review and Breakthrough Therapy Designation

HUTCHMED says China NMPA accepts sovleplenib wAIHA NDA for priority review

HUTCHMED (China) Ltd - Phase Trial for Sovleplenib in Waha Met Primary Endpoint in January 2026

THOMSON REUTERS

HUTCHMED (China) Ltd - Nda for Sovleplenib in Waha Accepted With Priority Review by Nmpa

THOMSON REUTERS

HUTCHMED Announces Nda Acceptance in China With Priority Review Status and Breakthrough Designation for Sovleplenib for the Treatment of Warm Antibody Autoimmune Hemolytic Anemia

THOMSON REUTERS

HUTCHMED to present new HMPL-A580 preclinical data at AACR annual meeting

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