HCM Hutchmed (China)
- 20.170
- -0.790-3.77%
- 20.170
- 0.0000.00%
Hutchmed (China) News
HUTCHMED's Breakthroughs in Hematology Spotlighted
Express News | Hehuang Pharmaceutical: Du Zhiqiang retires as chairman and executive director and will serve as the company's strategic advisor
Hutchmed (China) Chairman Simon To Resign; Dan Eldar Appointed Chairman
By Chris Wack Hutchmed (China) said Friday that Simon To has resigned as chairman and executive director and that Dan Eldar has been named as the company's new chairman effective immediately. The co
HUTCHMED Appoints New Chairman Amid Board Changes
Hehuang Pharmaceutical (00013) appoints Elder as new chairman
Hehuang Pharmaceutical (00013) issued an announcement. (a) Du Zhiqiang retired as chairman and executive director of the company after 23 years...
HUTCHMED to Present Promising Study Results at EHA2024
Hehuang Pharmaceutical (00013.HK): Will announce data on the 2024 European Hematology Association (EHA) ESLIM-01 phase III study and hematological malignancy project data
Gelonghui, May 17丨Hewang Pharmaceutical (00013.HK) announced today that it will announce the top line and subgroup results of the solepinib ESLIM-01 phase III study, as well as the latest and updated clinical data on innovative exploratory hematologic malignancy therapies HMPL-306, HMPL-760, and tazostat (tazostemetat) at the European Hematology Association (“EHA”) annual meeting to be held in Madrid and online from June 13 to June 16, 2024.
HUTCHMED Highlights Sovleplenib Phase III ESLIM-01 Study and Hematological Malignancy Programs Data to Be Presented at the Upcoming EHA2024 Congress
HUTCHMED (China) Limited ("HUTCHMED") (Nasdaq/AIM:HCM; HKEX:13) today announces that topline and subgroup results from the ESLIM-01 Phase III study of sovleplenib, as well as new and updated data related to novel investigational hematological malignancy therapies HMPL-306, HMPL-760 and tazemetostat, will be presented at the upcoming European Hematology Association ("EHA") Hybrid Congress, taking place on June 13-16, 2024 in Madrid, Spain and online.
Hehuang Pharmaceutical (00013.HK): ESLIM-01 study results released, long-lasting response rate is impressive
Core view: Incident: Chi-Med released phase III clinical data (ESLIM-01) of solepinib for primary thrombocytopenia (ITP) at the 2024 EHA conference. According to the one issued by Hewang Pharmaceuticals
Analysts' Opinions Are Mixed on These Healthcare Stocks: HUTCHMED (HCM) and PAVmed (PAVM)
Hutchmed Starts Phase 2/3 Trial of Surufatinib Combination Therapy in Pancreatic Cancer
Hutchmed (HCM) said Tuesday it started a phase 2/3 trial of its drug candidate surufatinib in combination with nab-paclitaxel, gemcitabine and Jiangsu Hengrui's camrelizumab as a first-line treatment
Reported Earlier, HUTCHMED Initiates The RAPHAEL Registrational Phase III Trial Of HMPL-306 For Patients With IDH1- And/Or IDH2-Mutated Relapsed/Refractory Acute Myeloid Leukemia In China
HMPL-306 is a novel dual-inhibitor of IDH1 and IDH2 enzymes. Mutations of IDH1 and IDH2 have been implicated as drivers of certain hematological malignancies, gliomas and solid tumors, particularly am
Reported Earlier, HUTCHMED Initiates Phase II/III Trial Of The Combination Of Surufatinib And Camrelizumab For Treatment-Naïve Pancreatic Ductal Adenocarcinoma In Collaboration With Hengrui
Almost half a million people diagnosed each year across the globe —Collaboration based on synergistic potential of inhibiting angiogenesis and tumor-associated macrophages with HUTCHMED's surufatinib
HUTCHMED Tests New Therapy for Pancreatic Cancer
Hutchmed Starts Phase 2/3 Trials for Pancreatic Cancer Drug in China; Shares Rise 3%
Hutchmed (HKG:0013) started its phase 2/3 trial for the combination of surufatinib and camrelizumab in patients with metastatic pancreatic ductal adenocarcinoma in China, according to a Tuesday filing
Hutchmed Begins Phase 3 Trials for Leukemia Medication in China
Hutchmed (HKG:0013) began its phase 3 trials for the HMPL-306 drug in patients with mutated isocitrate dehydrogenase 1 or 2 relapsed or refractory acute myeloid leukemia in China, according to a Tuesd
Express News | Galaxy Securities: Judging from the pace of the industry's revenue growth rate, the first quarter of 2024 is expected to be the lowest point in the pharmaceutical industry in the whole year
Hehuang Pharmaceutical (00013.HK): Initiating a RAPHAEL registered phase III study on HMPL-306 in the treatment of relapsed/refractory acute myeloid leukemia patients with IDH1 and/or IDH2 mutations in China
On May 14, Ge Longhui Pharmaceutical (00013.HK) announced today the launch of a registered phase clinical trial of HMPL-306 to treat relapsed/refractory acute myeloid leukemia (AML) with isocitrate dehydrogenase (“IDH”) 1 or 2 mutations in China. The first test subject received the first dose of medication on May 11, 2024.
Hehuang Pharmaceutical (00013.HK) and Hengrui Pharmaceutical reached a cooperation and initiated a phase II/III study on surufatinib (surufatinib) combined with camrelizumab (camrelizumab) in the treatment of primary pancreatic ductal adenocarcinoma
Gelonghui, May 14, 丨 Hehuang Pharmaceutical (00013.HK) announced the launch of a Chinese phase II/III clinical trial today to evaluate Hehuang Pharmaceutical's drug candidate surufatinib (surufatinib), the PD-1 antibody camrelizumab (camrelizumab) of Jiangsu Hengrui Pharmaceutical Co., Ltd. (“Hengrui Pharmaceutical”), albumin-conjugated paclitaxel (nab-paclitaxel), and gemcitabine (gemcitabine) for first-line treatment of metastatic pancreatic conduction Ductal adenocarcinoma (PDAC) patients
HUTCHMED Initiates Phase II/III Trial of the Combination of Surufatinib and Camrelizumab for Treatment-Naïve Pancreatic Ductal Adenocarcinoma in Collaboration With Hengrui
HUTCHMED (China) Limited (Nasdaq/AIM:HCM; HKEX:13) today announces the initiation of a Phase II/III trial to evaluate the efficacy of a combination of the HUTCHMED drug candidate surufatinib, the Jiangsu Hengrui Pharmaceuticals Co., Ltd PD-1 antibody camrelizumab, nab-paclitaxel and gemcitabine as a first-line treatment for patients with metastatic pancreatic ductal adenocarcinoma ("PDAC") in China.
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