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HUTCHMED (China) Limited - American Depositary Shares
(NQ:
HCM
)
16.06
UNCHANGED
Streaming Delayed Price
Updated: 4:00 PM EDT, Apr 1, 2025
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Press Releases about HUTCHMED (China) Limited - American Depositary Shares
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HUTCHMED Announces NMPA Conditional Approval for TAZVERIK® (tazemetostat) for the Treatment of Relapsed or Refractory Follicular Lymphoma
March 21, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
Intended Retirement of Independent Non-executive Directors and changes of composition of board committees
March 20, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Highlights Savolitinib SAVANNAH Phase II and Other Data at European Lung Cancer Congress 2025
March 19, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Reports 2024 Full Year Results and Provides Business Updates
March 19, 2025
65% oncology products revenue growth drove profitable operation and supported new ATTC platform
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED and Innovent Jointly Announce that the FRUSICA-2 Phase II/III Study of Fruquintinib and Sintilimab Combination Has Met its Primary Endpoint in Advanced Renal Cell Carcinoma in China
March 18, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces that it has Completed Enrollment of a Phase II Registration Study of Fanregratinib (HMPL-453) for Intrahepatic Cholangiocarcinoma in China
March 06, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces Appointment of Independent Non-executive Director and Member of Board Committee
March 05, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED to Announce 2024 Final Results
February 19, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces NMPA Full Approval for ORPATHYS® (savolitinib) in China for Patients with Locally Advanced or Metastatic MET Exon 14 NSCLC
January 13, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces NDA Acceptance in China with Priority Review Status for ORPATHYS® and TAGRISSO® Combination in Lung Cancer Patients with MET amplification After Progression on First-Line EGFR Inhibitor Therapy
January 01, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces US$608 million Divestment of Non-Core Joint Venture
January 01, 2025
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED to Receive Milestone Payment from Takeda following First European Reimbursement for FRUZAQLA® (fruquintinib)
December 12, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces Breakthrough Therapy Designation in China for ORPATHYS® and TAGRISSO® Combination in Certain Lung Cancer Patients After Disease Progression on EGFR Inhibitor Therapy
December 11, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED and Innovent Jointly Announce NMPA Conditional Approval for ELUNATE® (Fruquintinib) in Combination with TYVYT® (Sintilimab Injection) for the Treatment of Advanced Endometrial Cancer
December 03, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces Continued Inclusion of ORPATHYS® (savolitinib) in the National Reimbursement Drug List in China at Current Terms
November 28, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces Launch by Takeda of FRUZAQLA® (fruquintinib) in Japan
November 21, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces Appointment of Independent Non-executive Director and Member of Board Committee
November 20, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Highlights Clinical Data to be Presented at the 2024 ASH Annual Meeting and the 2024 ESMO Asia Congress
November 05, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED to Receive First Commercial Milestone Payment Following Over US$200 Million in FRUZAQLA® (fruquintinib) Sales by Takeda
October 31, 2024
— US$20 million payment based on sales of FRUZAQLA® in metastatic colorectal cancer —
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces that TAGRISSO® plus ORPATHYS® demonstrated high, clinically meaningful response rate in lung cancer patients with high levels of MET overexpression and/or amplification in SAVANNAH Phase II trial
October 16, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
Active Biotech Alert: FDA Approves 16 New Cancer Treatments as Global Cancer Rates Skyrocket
October 04, 2024
EQNX::TICKER_START (NASDAQ:ONCY),(TSX:ONC),(NYSE:ABBV),(NASDAQ:BGNE),(NASDAQ:HCM),(NASDAQ:ELVN) EQNX::TICKER_END
Via
FinancialNewsMedia
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HUTCHMED Announces Japan Approval for FRUZAQLA® (fruquintinib) Received by Takeda
September 24, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
Deutsche Bank ADR Virtual Investor Conference: Presentations Now Available for Online Viewing
September 26, 2024
Company Executives Share Vision and Answer Questions at VirtualInvestorConferences.com
From
Virtual Investor Conferences
Via
GlobeNewswire
HUTCHMED Highlights Clinical Data to be Presented at ESMO Congress 2024 and the 2024 World Conference of Lung Cancer
September 08, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
International companies to host live webcasts at Deutsche Bank’s Depositary Receipts Virtual Investor Conference on September 24th and 25th, 2024
September 17, 2024
From
Virtual Investor Conferences
Via
GlobeNewswire
HUTCHMED Provides Update on Fruquintinib for Second-Line Gastric Cancer in China
August 30, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED to Host Expert Call to discuss Immune Thrombocytopenia
August 21, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Reports 2024 Interim Results and Provides Business Updates
July 31, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED Announces NDA Acceptance in China for Tazemetostat for the Treatment of Relapsed or Refractory Follicular Lymphoma with Priority Review Status
July 03, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
HUTCHMED to Announce 2024 Half-Year Financial Results
June 26, 2024
From
HUTCHMED (China) Limited
Via
GlobeNewswire
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