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HUTCHMED

19.770

+0.0100.05%

Volume:3.31M

Turnover:65.16M

Market Cap:17.24B

PE:4.85

High:20.080

Open:20.080

Low:19.420

Close:19.760

52wk High:28.800

52wk Low:15.570

Shares:872.00M

HK Float Shares:872.00M

Volume Ratio:0.47

T/O Rate:0.38%

Dividend:- -

Dividend Rate:- -

EPS(LYR):4.077

ROE:1.46%

ROA:-1.24%

PB:1.74

PE(LYR):4.85

PS:4.00

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Overview Company News Filings

Hutchmed (China) - Reiterates Fy2026 Guidance for Oncology/Immunology Revenue of $330-$450 Mln

THOMSON REUTERS

Hutchmed (China) - Net Income Attributable to Hutchmed at $15.90 Mln in H1 2026

THOMSON REUTERS

Hutchmed China Ltd - Hutchmed Reports 2026 Interim Results

THOMSON REUTERS

Half-Year Report on the DBV Technologies Liquidity Contract with ODDO BHF

Hutchmed Gets China Nod for Gastric Cancer Drug Application

MT Newswires Live

HUTCHMED's Savolitinib Gains Conditional NMPA Approval for MET-Amplified Gastric Cancer

Hutchmed Says China Regulator Grants Conditional Approval for Orpathys in Met-amplified Gastric Cancer

Hutchmed Announces Nmpa Approval for Orpathys® for the Treatment of Gastric Cancer Patients with Met Amplification

THOMSON REUTERS

HUTCHMED Announces NMPA Approval for ORPATHYS® for the treatment of Gastric Cancer Patients with MET Amplification

HUTCHMED Sets 30 July Board Meeting to Approve 2026 Interim Results; Webcast Details Announced

Bulletin Express

Hutchmed Schedules Webcast Presentation Following Interim Results Announcement

Hutchmed China Ltd - Hutchmed to Announce 2026 Half-year Results

THOMSON REUTERS

Hutchmed to Announce 2026 Half-year Financial Results

THOMSON REUTERS

HUTCHMED to Announce 2026 Half-Year Financial Results

Hutchmed Says Phase II Fanregratinib Trial in Fgfr2-altered Bile Duct Cancer Posts 42.5% Response Rate

HUTCHMED Highlights Pivotal Phase II Data for Fanregratinib in Intrahepatic Cholangiocarcinoma Presented at ESMO Gastrointestinal Cancers Congress 2026

Hutchmed Unveils Phase III Data for Sovleplenib in wAIHA at 2026 EHA Congress

HUTCHMED’s sovleplenib delivers 66% durable hemoglobin response in Phase III warm AIHA trial; China NDA under priority review

Bulletin Express

HUTCHMED says China regulator accepts sovleplenib NDA for wAIHA, grants priority review

HUTCHMED says Phase III ESLIM-02 trial shows sovleplenib lifts durable response in warm autoimmune hemolytic anemia

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Breakthrough Therapy Designation granted in March 2026.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. HUTCHMED  Ltd. published the original content used to generate this news brief via IIS, the regulatory disclosure system operated by the Hong Kong Stock Exchange  , on June 12, 2026, and is solely responsible for the information contained therein.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260612:nNDLnbGTv:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","00013","BK1587","BK1588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642230204","title":"HUTCHMED says Phase III ESLIM-02 trial shows sovleplenib lifts durable response in warm autoimmune hemolytic anemia","url":"https://stock-news.laohu8.com/highlight/detail?id=2642230204","media":"Reuters","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642230204?lang=en_us&edition=fundamental","pubTime":"2026-06-12 08:00","pubTimestamp":1781222418,"startTime":"0","endTime":"0","summary":"HUTCHMED highlighted Phase III results for sovleplenib in warm autoimmune hemolytic anemia, already presented at the EHA 2026 Congress on June 11.The trial showed the drug delivered faster, more sustained improvement in hemoglobin control than placebo, with fewer relapses and less need for rescue treatment.Patients on sovleplenib also required fewer blood transfusions and were more likely to reduce or stop background steroid use.Safety was described as favorable, with fewer severe adverse events than placebo and no treatment-related deaths or discontinuations reported.China’s NMPA accepted an NDA for sovleplenib in April 2026, granting priority review for adults with inadequate response to prior glucocorticoids.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260612:nNDL172BhR:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SG9999014021.USD","IE00BN0W2T93.GBP","LU2210150020.SGD","00013","IE00BKPKM429.USD","SG9999014039.USD","BK4588","SG9999014013.SGD","BK4112","LU2095319765.USD","BK1588","SG9999014005.SGD","NDAQ","IE00B64PRP62.GBP","IE00B3QW5Z07.USD","LU0314104364.USD","IE00BN0W2V16.EUR","BK4585","IE00BGHQF748.EUR","BK1191","BK1587","IE00BN0W2W23.USD","LU2210149790.SGD"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":7,"pageCount":2,"totalSize":123,"code":"91000000","status":"200"}]}}