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Hutchmed (HCM) Share News

Hutchmed announces trials of HMPL-306 and Surufatinib cancer therapies

14th May 2024 14:33

(Alliance News) - Hutchmed (China) Ltd on Tuesday announced upcoming trials for two of its pipeline cancer treatments, both of which it believes could fill significant clinical gaps. Read More

UK shareholder meetings calendar - next 7 days

3rd May 2024 13:37

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Hutchmed notes CHMP's positive opinion for fruiquintinib approval

26th Apr 2024 16:09

(Alliance News) - Hutchmed (China) Ltd on Friday said that its partner Takeda Pharmaceutical Co Ltd has been notified that the Committee for Medicinal Products for Human Use of the European Medicines Agency recommends approval for fruquintinib. Read More

Hutchmed endometrial cancer treatment application accepted for review

2nd Apr 2024 10:32

(Alliance News) - Hutchmed (China) Ltd on Tuesday jointly announced with Innovent Biologics that their new drug application for the combined fruquintinib and sintilimab treatment for endometrial cancer has been granted priority review by the China National Medical Products Administration. Read More

LONDON BRIEFING: HSBC in special payout on Canada sale; Astra FDA win

2nd Apr 2024 08:05

(Alliance News) - London's FTSE 100 traded higher on Tuesday following the long weekend, as investors react to US data, and look ahead to manufacturing sector readings from Europe later. Read More

Hutchmed lung cancer treatment accepted for review in China

28th Mar 2024 11:08

(Alliance News) - Hutchmed (China) Ltd on Thursday said its supplemental new drug application for savolitinib has been accepted for review by the China National Medical Products Administration. Read More

LONDON BRIEFING: JD Sports backs outlook; Spirent accepts new offer

28th Mar 2024 08:08

(Alliance News) - Stocks in London traded higher early on Thursday in the final trading day of a holiday-shortened week, despite some hawkish words from a US central banker. Read More

Hutchmed begins registration stage for sovleplenib phase 2/3 trial

22nd Mar 2024 10:09

(Alliance News) - Hutchmed (China) Ltd on Friday said it initiated the registration stage of the phase 2/3 clinical trial for sovleplenib, its warm antibody autoimmune hemolytic anemia treatment. Read More

EARNINGS: Hutchmed revenue surges, Craven House's loss widens

28th Feb 2024 17:31

(Alliance News) - The following is a round-up of updates by London-listed companies, issued on Wednesday and not separately reported by Alliance News: Read More

UK earnings, trading statements calendar - next 7 days

21st Feb 2024 15:14

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Hutchmed hails fruquintinib trial results for gastric cancer treatment

7th Feb 2024 09:50

(Alliance News) - Hutchmed (China) Ltd on Wednesday said phase three data for fruquintinib in combination with paclitaxel showed an improvement in overall survival for patients with gastric or gastroesophageal junction adenocarcinoma. Read More

Hutchmed says Inmagene exercises option to licence drug candidates

2nd Feb 2024 09:52

(Alliance News) - Hutchmed (China) Ltd on Friday said Inmagene Biopharmaceuticals Ltd has exercised options to licence two drug candidates as part of a strategic partnership. Read More

Hutchmed celebrates cancer drug approval in hometown of Hong Kong

30th Jan 2024 09:20

(Alliance News) - Hutchmed (China) Ltd on Tuesday touted progress in Hong Kong, after its oral therapy for metastatic colorectal cancer received marketing approval in the city. Read More

TOP NEWS: Hutchmed Sovleplenib accepted for review by China drug bureau

11th Jan 2024 10:17

(Alliance News) - Hutchmed Ltd on Thursday said that its novel treatment for haematological malignancies and immune diseases had been progressed to the next stage of approval by the country's national bureau for drug supervision. Read More

IN BRIEF: Hutchmed China renews deals with "substantial" shareholders

21st Dec 2023 11:36

Hutchmed (China) Ltd - Hong Kong-based developer of treatments for cancer and immunological diseases - Agrees with "substantial shareholder" Sinopharm Group Co Ltd to renew the Framework Sinopharm Products Supply & Purchase Agreement, effective from January 1, for three years up to and including December 31, 2026. Also agrees with HCMH to renew the HBYS Brand License Royalty agreement, also effective from January 1 and for the same duration. HCMH entered the HBYS deal in June 2021 with HWEL, a subsidiary of major shareholder CK Hutchison Holdings Ltd which holds an approximate 38.18% stake in Hutchmed. Read More

Hutchmed completes enrolment for fruquintinib trial

13th Dec 2023 13:56

(Alliance News) - Hutchmed (China) Ltd on Wednesday said it has completed enrolment of its phase II/III trial of fruquintinib. Read More

Hutchmed hails Takeda's fruquintinib approval from US for cancer form

9th Nov 2023 12:16

(Alliance News) - Hutchmed (China) Ltd on Thursday announced that the Tokyo-based drug maker, Takeda Pharmaceutical Co Ltd, has received US approval of fruquintinib for a form of colorectal cancer. Read More

Hutchmed notes Takeda submits fruquintinib drug application in Japan

29th Sep 2023 10:12

(Alliance News) - Hutchmed (China) Ltd on Friday said Takeda Pharmaceutical Co Ltd has submitted a new drug application for cancer treatment fruquintinib to the Ministry of Health, Labour & Welfare in Japan. Read More

IN BRIEF: Hutchmed China finalises patient enrolment for Tazemetostat

12th Sep 2023 10:26

Hutchmed (China) Ltd - Hong Kong-based developer of treatments for cancer and immunological diseases - Completes patient enrolment for bridging phase two study in China to evaluate the efficacy of cancer drug Tazemetostat for the treatment of patients with relapsed/refractory follicular lymphoma. Tazemetostat is approved by the US Food & Drug Administration for the treatment of advanced epithelioid sarcoma and R/R FL. Read More

IN BRIEF: China grants Hutchmed's savolitinib breakthrough therapy tag

29th Aug 2023 09:30

Hutchmed (China) Ltd - Hong Kong-based developer of treatments for cancer and immunological diseases - Wins 'breakthrough therapy designation' in China for its gastric cancer treatment, savolitinib. The BTD is granted by the National Medical Products Administration. It is for the treatment of locally advanced or metastatic gastric cancer or gastroesophageal junction adenocarcinoma patients with mesenchymal epithelial transition factor amplification who have failed at least two lines of standard therapies. Hutchmed notes that MET-driven gastric cancer has a poor prognosis, and China grants a BTD to new drugs that treat life-threatening diseases for which there are no effective treatment options. Read More

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