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倫敦:2019年11月28日,星期四:和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」)(AIM/Nasdaq: HCM)今天宣佈其用於治療晚期結直腸癌的國家1類靶向抗癌藥物愛優特®(呋喹替尼膠
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倫敦:2019年11月25日,星期一:和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」) (AIM/Nasdaq: HCM) 今天宣佈索凡替尼獲美國食品藥品監督管理局(「FDA」)授予孤兒藥資格用於
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倫敦:2019年11月23日,星期六:和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」) (AIM/Nasdaq: HCM) 將於2019年11月22日至24日在新加坡舉行的第五届歐洲腫瘤內科學會(「ESMO 」)
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倫敦:2019年11月11日,星期一:和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」)(AIM/Nasdaq: HCM)今日宣布,中國國家藥品監督管理局(NMPA)已受理索凡替尼(surufatinib)用於治療
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倫敦,2019年10月17 日,星期四 :和黃中國醫藥科技有限公司 (簡稱“和黃醫藥”或“Chi-Med”) (AIM/納斯達克: HCM)今日重點介紹於美國癌症研究協會的期刊《癌症發現(Cancer Discovery)》[1] 發表
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中國蘇州及英國倫敦,2019年10月10日,星期四:信達生物製藥(「信達生物」)(香港聯交所股票代碼:01801)與和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」)(AIM/納斯達克
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倫敦,2019年10月4日,星期五:和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」) (AIM/Nasdaq:HCM)啟動了一項HMPL-523治療復發性或難治性淋巴瘤患者的國際I/Ib期臨床試驗。HMPL-52
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– 索凡替尼在III期臨床試驗SANET-ep中達到了主要終點,幫助降低非胰腺神經內分泌瘤(「NET」)患者的疾病進展或死亡風險達67% – –目前正籌備計劃於2019年底前提交索凡替尼用於非胰腺神
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—即將發表關於索凡替尼治療非胰腺神經內分泌腫瘤患者的SANET-ep III期臨床試驗積極結果的最新摘要— —將於9月30日(星期一)聯同試驗主要研究者舉行電話會議和網絡音頻直播,共同解
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倫敦:2019年9月18日(星期三):和黃中國醫藥科技有限公司(簡稱「和黃醫藥」或「Chi-Med」) (AIM/Nasdaq:HCM) 將於2019年9月18-22日在中國廈門舉行的第22屆全國臨床腫瘤學大會暨2019年CSCO學
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倫敦,2019年9月3日(星期二):和黃中國醫藥科技有限公司(簡稱和黃醫藥「Chi-Med」) (AIM/Nasdaq:HCM) 啟動了一項HMPL-689治療復發性或難治性淋巴瘤患者的國際I/Ib期臨床試驗。 HMPL-689是一種作
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倫敦,2019年8月23日 (星期五):和黃中國醫藥科技有限公司 (簡稱 「和黃醫藥」 或「Chi-Med」) (AIM/Nasdaq: HCM) 在中國啟動了一項HMPL-523治療免疫性血小板減少性紫癜 (「ITP」) 患者的I期臨床試驗
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香港:2019 年6 月14 日,星期五:和黃中國醫藥科技有限公司(Chi-Med)(AIM /納斯達克股票代碼:HCM)今日宣布索凡替尼以晚期非胰腺神經內分泌瘤為適應症的III 期關鍵性研究SANET-ep 預設的
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2019年3月29日,中國上海 — 和黃中國醫藥科技有限公司(Chi-Med)(AIM/NASDAQ: HCM)子公司和記黃埔醫藥在中國啟動了一項有註冊性潛力的IIb/III期臨床試驗,旨在對比索凡替尼(HMPL-012或sulfat
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2019年3月28日,中國上海 — 和黃中國醫藥科技有限公司 (Chi-Med)(AIM/NASDAQ: HCM) 子公司和記黃埔醫藥將於2019年3月31日-4月3日在美國佐治亞州亞特蘭大市召開的美國癌症研究協會(AACR)
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香港:2019年2月12日,星期二:和黃中國醫藥科技有限公司 (Chi-Med)(AIM/NASDAQ: HCM)今日宣佈CALYPSO II期臨床研究中探索沃利替尼/Imfinzi®(durvalumab)聯合療法治療轉移性乳頭狀腎細胞癌(PRCC
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– Chi-Med acquires right to determine & conduct all future life cycle indication development of fruquintinib monotherapy as well as innovative combinations in China –  – Chi-Med to assume all development costs of life cycle indications in
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– Global SAVANNAH study of savolitinib / Tagrisso®combination in MET+ EGFRm NSCLC underway. Data presented at ESMO 2018 showedMET-amplification among the most frequent mechanisms of acquired resistance to AstraZeneca’s Tagrisso® – – China
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London: Thursday, November 29, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) entered into four collaboration agreements to evaluate the safety, tolerability and efficacy of Chi-Med’s surufatinib (HMPL-012 or sulfatinib) a
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London: Monday, November 26, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces the first commercial launch of fruquintinib capsules (Elunate®) with the initiation of product sales in China. Elunate® is for the
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Shanghai: November 20, 2018: Hutchison China MediTech (“Chi-Med”) received “R&D Achievement of the Year” Award from BayHelix at the BioCentury China Healthcare Summit on November 14, 2018. Hutchison MediPharma, the Innovation Platform
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– Trial did not meet the primary endpoint of overall survival despite improvement in progression-free survival – London: Friday, November 16, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces the outcome of
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London: Thursday, October 18, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) has initiated a Phase I study of HMPL-523, its novel spleen tyrosine kinase (“Syk”) inhibitor, in combination with azacitidine, an approved nuc
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– Fruquintinib capsules provide a new oral treatment option for patients with metastatic colorectal cancer and will be marketed as Elunate® – – Elunate® data published in JAMA demonstrated increased overall survival versus placebo – – F
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London: Monday, July 23, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) has initiated a Phase Ib/II proof-of-concept study of sulfatinib in pancreatic neuroendocrine tumors (“NET”) patients and in biliary tract cancer (
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Press Release – Chi-Med makes additional FRESCO presentations at ASCO 2018, following oral presentation at ASCO 2017 showing that study met all endpoints with a manageable safety profile and lower off-target toxicities compared to other targeted t
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London: Tuesday, March 6, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) has initiated a Phase Ib/II proof-of-concept study of epitinib in glioblastoma patients with epidermal growth factor receptor (“EGFR”) gene amplifi
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London: Tuesday, February 13, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) has completed patient enrollment of FALUCA, its Phase III pivotal trial of fruquintinib in advanced, third-line, non-small cell lung cancer (“NSC
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London: Friday, December 15, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) has initiated the United States Phase I bridging clinical trial of fruquintinib. Fruquintinib is a highly selective and potent oral inhibitor of vas
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London: Tuesday, October 31, 2017: Hutchison China MediTech Limited (“Chi‑Med”) (AIM/Nasdaq: HCM) has initiated FRUTIGA, a pivotal Phase III clinical trial of fruquintinib in combination with paclitaxel (Taxol®) for the treatment in advanced g
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– Data for savolitinib in combination with Tagrisso® or Iressa® presented at World Conference on Lung Cancer –  – New data give insights into disease progression and potential next-generation treatment strategies in patients with EGFR-muta
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Press Release – Fruquintinib in combination with Iressa® (gefitinib) shows promising efficacy and an acceptable safety profile – – Further validation of strong potential for use of fruquintinib in combination with other cancer therapies du
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Press Release   – Three oral presentations given at CSCO for fruquintinib, savolitinib and theliatinib – – Plenary keynote presentation for FRESCO Phase III trial details analysis showing consistent survival benefit in all key subgroups
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Press Release – Data to show potential of savolitinib to treat EGFR-TKI resistance in both Iressa® and Tagrisso® refractory patients with MET amplification – – Results to further validate Chi-Med’s scientific strategy of designing highly
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Press Release London: Tuesday, August 29, 2017: Hutchison China MediTech Limited (“Chi‑Med”) (AIM/Nasdaq: HCM) has initiated a Phase I clinical trial of HMPL‑689 in China. HMPL-689 is a novel, highly selective and potent small molecule inhib
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AstraZeneca PLC (“AstraZeneca”) (LON/STO/NYSE: AZN) Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM)   London: Thursday, June 29, 2017: Chi-Med and AstraZeneca today announce that they have initiated
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Press Release London: Thursday, June 22, 2017: Hutchison China MediTech Limited (“Chi‑Med”) (AIM/Nasdaq: HCM) has just initiated a Phase I/II clinical trial of HMPL‑453 in China.  HMPL‑453 is a novel, highly selective and potent small mol
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– Application accepted by CFDA for technical review by the Center for Drug Evaluation – – Triggers RMB30.8 million milestone payment from Eli Lilly and Company (“Lilly”) – London: Monday, June  12, 2017: Hutchison China MediTech L
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Press Release Chicago: Monday, June 5, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announced that results from its pivotal Phase III trial with fruquintinib, its novel vascular endothelial growth factor receptor (“VEGF
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London: Friday, April 7, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) presented pre-clinical data for fruquintinib and sulfatinib at the American Association for Cancer Research (“AACR”) Annual Meeting 2017, held in Wa
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Press Release London: Tuesday, March 21, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that it will host Research & Development (“R&D”) briefings in London and New York to provide an overview o
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– Trial met all primary and secondary endpoints – – Safety as expected – – Progressing to China NDA submission mid-2017 – – Full data to be reported at an upcoming scientific meeting in mid-2017 – London: Friday, March 3, 2017: Hu
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Press Release London: Monday, February 20, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that a Phase II study of savolitinib has been initiated in locally advanced or metastatic pulmonary sarcomatoid carci
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London: Tuesday, February 14, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that it has initiated the first-in-human (“FIH”) Phase I clinical trial of HMPL-453 in Australia.  HMPL-453 is a novel, highly
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Press Release London: Tuesday, February 14, 2017:  Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) and AstraZeneca PLC (“AstraZeneca”) will present data from the ongoing Phase II clinical trial of savolitinib in patients wi
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London: Monday, January 16, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq:HCM) today announces that it has initiated a Phase II study of a combination therapy using fruquintinib and Iressa® in the first-line setting for patients
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London: Monday, January 16, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that it has initiated a Phase II study of sulfatinib in second-line biliary tract cancer (“BTC”) patients in China.  Sulfatinib
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London: Monday, January 16, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that data from the ongoing Phase I/II clinical trial of fruquintinib in combination with paclitaxel (Taxol®) in second-line patients
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London: Tuesday, January 10, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that it has initiated a Phase I trial of its novel spleen tyrosine kinase (“Syk”) inhibitor, HMPL-523, in patients with hematolo
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Press Release London: Tuesday, December 6, 2016: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that data from a recent pre-clinical study, investigating the in vitro and in vivo anti-tumor activities of novel Spl
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