HCM
NASDAQHUTCHMED (China) Limited
Price$10.86-0.05 (-0.46%)
02:00 PM07:45 PM
News · 26 weeks56+75%
2026-01-182026-07-12
Mix2690d
- SEC Filings12(46%)
- Other9(35%)
- Insider5(19%)
Latest news
25 items- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED Announces NMPA Approval for ORPATHYS® for the treatment of Gastric Cancer Patients with MET AmplificationHONG KONG and SHANGHAI and FLORHAM PARK, N.J., July 02, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces that the New Drug Application (NDA) for ORPATHYS® (savolitinib) has been granted conditional approval by the China National Medical Products Administration ("NMPA") for the treatment of locally advanced or metastatic gastric cancer or gastroesophageal junction (GC/GEJ) adenocarcinoma patients with MET amplification who have failed at least two prior systemic treatments. Gastric cancer remains one of the most common cancers and leading causes of cancer death in China. MET-driven gastric cancer has a very poor prognosis.1 It is esti
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED to Announce 2026 Half-Year Financial ResultsHONG KONG and SHANGHAI and FLORHAM PARK, N.J., June 30, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM: HCM; HKEX:13) will announce its interim results for the six months ended June 30, 2026 on Thursday, July 30, 2026 at 7:00 am Eastern Daylight Time (EDT) / 12:00 noon British Summer Time (BST) / 7:00 pm Hong Kong Time (HKT). HUTCHMED management will host two webcast presentations for analysts and investors to discuss the interim results, followed by Q&A sessions. The English webcast will be held on Thursday, July 30, 2026, at 8:00 am EDT / 1:00 pm BST / 8:00 pm HKT. The Chinese (Putonghua) webcast will be held at 8:30 am HKT on Friday, July 31, 2026 (1:30 am
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED Highlights Pivotal Phase II Data for Fanregratinib in Intrahepatic Cholangiocarcinoma Presented at ESMO Gastrointestinal Cancers Congress 2026— Registration-enabling study demonstrated high clinically meaningful objective responses, achieving rapid and durable disease control — — Fanregratinib holds promise as a new treatment option for pretreated advanced ICC patients harboring FGFR2-fusions/rearrangements — HONG KONG and FLORHAM PARK, N.J., June 25, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces results from the pivotal Phase II registration study of fanregratinib (HMPL-453) in patients with intrahepatic cholangiocarcinoma ("ICC") will be presented at the European Society for Medical Oncology (ESMO) Gastrointestinal Cancers Congress taking place from July 1 to 4, 2026
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED Highlights Sovleplenib ESLIM-02 Phase III Data in Warm Antibody Autoimmune Hemolytic Anemia Presented at EHA 2026 Congress— Sovleplenib demonstrated rapid and durable hemoglobin response with favorable safety profile — —The ESLIM-02 study underscores sovleplenib's potential to address critical unmet needs in a treatment landscape currently devoid of approved targeted therapies — HONG KONG and SHANGHAI and FLORHAM PARK, N.J., June 12, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces results from the Phase III part of the ESLIM-02 study of sovleplenib in patients with warm antibody autoimmune hemolytic anemia ("wAIHA") in China were presented on Thursday, June 11, 2026 during the European Hematology Association ("EHA") Congress in Stockholm, Sweden. S
- SECSEC Form S-8 filed by HUTCHMED (China) LimitedS-8 - HUTCHMED (China) Ltd (0001648257) (Filer)
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED Highlights Clinical Data to be Presented at the 2026 ASCO Annual MeetingHONG KONG and FLORHAM PARK, N.J., May 22, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces that new and updated data from several studies of compounds discovered by HUTCHMED will be presented at the American Society of Clinical Oncology ("ASCO") Annual Meeting taking place from May 29 to June 2, 2026 in Chicago, USA. Results from the pivotal Phase II registration study of savolitinib in gastric cancer or gastroesophageal junction adenocarcinoma patients with MET amplification in China will be presented during a rapid oral session. The study met its primary endpoint of objective response rate ("ORR") per RECIST 1.1, as assessed by the
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- INSIDERSEC Form 4 filed by Acting CEO and CFO Cheng Chig Fung4 - HUTCHMED (China) Ltd (0001648257) (Issuer)
- INSIDERSEC Form 4 filed by Group General Counsel Nixon Charles George Rupert4 - HUTCHMED (China) Ltd (0001648257) (Issuer)
- INSIDERSEC Form 4 filed by CEO and CSO Su Wei-Guo4 - HUTCHMED (China) Ltd (0001648257) (Issuer)
- INSIDERSEC Form 4 filed by Deputy Chief Financial Officer Chiu Lorenso4 - HUTCHMED (China) Ltd (0001648257) (Issuer)
- PRHUTCHMED 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 CarcinomaHONG KONG and SHANGHAI and FLORHAM PARK, N.J., May 21, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) and Innovent Biologics, Inc. ("Innovent", HKEX:1801) today jointly announce that the New Drug Application (NDA) for the combination of ELUNATE® (fruquintinib) and TYVYT® (sintilimab injection) has been granted approval by the China National Medical Products Administration ("NMPA") for the treatment of patients with locally advanced or metastatic renal cell carcinoma who have failed prior vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFR-TKI) therapy and have not received programmed death receptor-1 ("PD-1") or programmed
- INSIDERSEC Form 4 filed by Former Director Mok Tony Shu Kam4 - HUTCHMED (China) Ltd (0001648257) (Issuer)
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRDeutsche Bank ADR Virtual Investor Conference: Presentations Now Available for Online ViewingNEW YORK, April 29, 2026 (GLOBE NEWSWIRE) -- Virtual Investor Conferences, the leading proprietary investor conference series, today announced the presentations from the Depositary Receipts Virtual Investor Conference ("dbVIC") held April 28th are now available for online viewing. VIEW PRESENTATIONS HERE The company presentations will be available 24/7 for 90 days. Investors, advisors, and analysts may download investor materials from the company's resource section. April 28th Company Presentations Lotus Technology Inc. (NASDAQ:LOT)Viomi Technology Co., Ltd (NASDAQ:VIOT)Belite Bio, Inc (NASDAQ:BLTE)First Pacific Company Ltd ((HKEX: 142, OTC:FPAFY)HUTCHMED (China) Limited (AIM:
- SECSEC Form 6-K filed by HUTCHMED (China) Limited6-K - HUTCHMED (China) Ltd (0001648257) (Filer)
- PRHUTCHMED Announces NDA Acceptance in China with Priority Review Status and Breakthrough Designation for Sovleplenib for the Treatment of Warm Antibody Autoimmune Hemolytic AnemiaHONG KONG and SHANGHAI and FLORHAM PARK, N.J., April 29, 2026 (GLOBE NEWSWIRE) -- HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces that the New Drug Application ("NDA") for sovleplenib for the treatment of adult patients with warm antibody autoimmune hemolytic anemia ("wAIHA") who have had an insufficient response to at least one previous glucocorticoid treatment has been accepted for review and granted priority review by the China National Medical Products Administration ("NMPA"). Sovleplenib is a novel, selective, oral inhibitor targeting spleen tyrosine kinase ("Syk"), being developed for the treatment of immune diseases and hematological malignancies.
HCM FAQ
7 questionsWhat does HUTCHMED (China) Limited do?
HUTCHMED (China) Limited discovers, develops, and commercializes targeted therapeutics and immunotherapies for cancer and immunological diseases worldwide. It operates in two segments, Oncology/Immunology and Other Ventures. It manufactures, distributes, markets, and sells prescription and over-the-counter pharmaceutical, and consumer health products. The company develops Savolitinib, an inhibitor for non-small cell lung cancer (NSCLC), papillary and clear cell renal cell carcinoma, colorectal cancer (CRC), and gastric cancer (GC); and Fruquintinib, an inhibitor for CRC, breast cancer, GC...Where does HCM stock trade?
HUTCHMED (China) Limited (HCM) is listed on NASDAQ.What sector and industry is HCM in?
HUTCHMED (China) Limited operates in the Health Care sector, Biotechnology: Pharmaceutical Preparations industry.When did HUTCHMED (China) Limited go public?
HUTCHMED (China) Limited (HCM) completed its IPO in 2016.What are analysts saying about HCM?
HUTCHMED (China) Limited has had 6 recent analyst actions on file. The most recent action was from Morgan Stanley: Underweight with a $1375.00 price target on 2025-09-22. Recent price targets range from $1375.00 to $4600.00.What companies are similar to HCM?
Notable peers in the same industry include LLY (Eli Lilly and Company), JNJ (Johnson & Johnson), ABBV (AbbVie Inc.), MRK (Merck & Company Inc.), NVS (Novartis AG). Compare HCM side-by-side with any of them on Quantisnow.How can I track HCM on Quantisnow?
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