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FinancialContent

HUTCHMED (China) Limited - American Depositary Shares (NQ:HCM)

13.59 +0.27 (+2.03%)
Delayed Quote Updated: 4:00 PM EDT, Oct 29, 2026 Add to My Watchlist
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All News about HUTCHMED (China) Limited - American Depositary Shares

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HUTCHMED Announces Sovleplenib Granted US FDA Orphan Drug Designation for Primary Immune Thrombocytopenia
From HUTCHMED (China) Limited
Via GlobeNewswire
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Save the Date: HUTCHMED to Host Expert Insights Event on Recent Savolitinib Clinical Data in Non-Small Cell Lung Cancer
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights SANOVO Phase III Data for ORPATHYS® plus TAGRISSO® in First-Line EGFR-Mutated Lung Cancer Presented at ESMO Congress 2026
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights SAFFRON Global Phase III Data Presented at ESMO Congress 2026 and Simultaneously Published in The New England Journal of Medicine
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces Closing of KRAS-EGFR-Antibody Conjugate Therapy License to GSK Outside China
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces Submission of US NDA for ORPATHYS® plus TAGRISSO® in MET-Driven EGFR-Mutated Lung Cancer
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Initiates Global Trial of KRAS-EGFR-Antibody Conjugate Therapy HMPL-A830 in Patients with Solid Tumors
First-in-class KRAS-payload leveraging synchronized EGFR inhibition 
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights Clinical Data to be Presented at the ESMO Congress 2026
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Lands GSK Deal Worth Up to $1.3B for KRAS-EGFR Cancer Therapy ↗
HUTCHMED (NASDAQ:HCM) said it has entered a co-development and licensing agreement with GSK for ex-China rights to HMPL-A830, a preclinical KRAS-EGFR antibody-targeted therapy conjugate, or ATTC. The... 
Via MarketBeat
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HUTCHMED Announces Licensing Agreement with GSK for KRAS-EGFR-Antibody Conjugate Cancer Therapy
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces SANOVO Trial Demonstrated Significant Progression-Free Survival Benefit of ORPATHYS® Plus TAGRISSO® in Treatment-Naïve Patients with MET-Overexpressing EGFR-mutated Lung Cancer in China
Findings build on the established success of the global SAFFRON and China SACHI trials, extending the clinical value of the all-oral combination into the first-line setting 
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces NMPA Approval for ATLED® (Fanregratinib) for the Treatment of Patients with FGFR2-Fusion/Rearrangement Intrahepatic Cholangiocarcinoma
Novel, highly potent oral selective FGFR 1/2/3 inhibitor approved for patients with advanced FGFR2-altered intrahepatic cholangiocarcinoma in China 
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces ORPATHYS® Plus TAGRISSO® Demonstrated Statistically Significant and Clinically Meaningful Improvements in Progression-Free and Overall Survival in MET-Driven EGFR-Mutated Lung Cancer After Progression on TAGRISSO®
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED H1 Earnings Call Highlights ↗
HUTCHMED (NASDAQ:HCM) reported first-half 2026 oncology revenue of $162 million, including $121 million in product revenue, as growth in China and expanding international sales of FRUZAQLA supported... 
Via MarketBeat
Topics Earnings
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HUTCHMED Reports 2026 Interim Results
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces NMPA Approval for ORPATHYS® for the treatment of Gastric Cancer Patients with MET Amplification
First selective MET inhibitor approved for patients with MET-amplified advanced gastric cancer or gastroesophageal junction adenocarcinoma in China 
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED to Announce 2026 Half-Year Financial Results
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights Pivotal Phase II Data for Fanregratinib in Intrahepatic Cholangiocarcinoma Presented at ESMO Gastrointestinal Cancers Congress 2026
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights Sovleplenib ESLIM-02 Phase III Data in Warm Antibody Autoimmune Hemolytic Anemia Presented at EHA 2026 Congress
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Highlights Clinical Data to be Presented at the 2026 ASCO Annual Meeting
From HUTCHMED (China) Limited
Via GlobeNewswire
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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
Reduced risk of disease progression or death by 63%, with median PFS of 22.2 months in the FRUSICA-2 registration study 
From HUTCHMED (China) Limited
Via GlobeNewswire
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Deutsche Bank ADR Virtual Investor Conference: Presentations Now Available for Online Viewing
Company Executives Share Vision and Answer Questions at VirtualInvestorConferences.com 
From Virtual Investor Conferences
Via GlobeNewswire
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HUTCHMED Announces NDA Acceptance in China with Priority Review Status and Breakthrough Designation for Sovleplenib for the Treatment of Warm Antibody Autoimmune Hemolytic Anemia
From HUTCHMED (China) Limited
Via GlobeNewswire
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International companies to host live webcasts at Deutsche Bank’s Depositary Receipts Virtual Investor Conference on April 28, 2026
From Virtual Investor Conferences
Via GlobeNewswire
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HUTCHMED Highlights Data to be Presented at AACR Annual Meeting 2026
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Initiates Phase III Trial of HMPL-760 in Patients with Relapsed/Refractory Diffuse Large B-cell Lymphoma in China
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Announces Update on Licensed Oncology Product TAZVERIK® in China
From HUTCHMED (China) Limited
Via GlobeNewswire
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Intended Retirement of Independent Non-executive Director and changes of composition of board committees
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Reports 2025 Full Year Results and Business Updates
From HUTCHMED (China) Limited
Via GlobeNewswire
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HUTCHMED Initiates Global Trial of PI3K/PIKK-EGFR ATTC Candidate HMPL-A580 in Patients with Solid Tumors
From HUTCHMED (China) Limited
Via GlobeNewswire
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