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伦敦:2019年11月28日,星期四:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”)(AIM/Nasdaq: HCM)今天宣布其用于治疗晚期结直肠癌的国家1类靶向抗癌药物爱优特®(呋喹替尼胶
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伦敦:2019年11月25日,星期一:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”) (AIM/Nasdaq: HCM) 今天宣布索凡替尼获美国食品药品监督管理局(“ FDA”)授予孤儿药资格用于
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伦敦:2019年11月23日,星期六:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med ”) (AIM/Nasdaq: HCM) 将于2019年11月22日至24日在新加坡举行的第五届欧洲肿瘤内科学会(“ESMO ”)
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伦敦:2019年11月11日,星期一:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”)(AIM/Nasdaq: HCM)今日宣布,中国国家药品监督管理局(NMPA)已受理索凡替尼(surufatinib)用于治疗
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伦敦,2019年10月17 日,星期四 :和黄中国医药科技有限公司 (简称“和黄医药”或“Chi-Med”) (AIM/纳斯达克: HCM)今日重点介绍于美国癌症研究协会的期刊《癌症发现(Cancer Discovery)》[1] 发表
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中国苏州及英国伦敦,2019年10月10日,星期四:信达生物制药(“信达生物“)(香港联交所股票代码:01801)与和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”)(AIM/纳斯达
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伦敦,2019年10月4日,星期五:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”) (AIM/Nasdaq:HCM)启动了一项HMPL-523治疗复发性或难治性淋巴瘤患者的国际I/Ib期临床试验。HMPL-523是
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– 索凡替尼在III期临床试验SANET-ep中达到了主要终点,帮助降低非胰腺神经内分泌瘤(“NET”)患者的疾病进展或死亡风险达67% – –目前正筹备计划于2019年底前提交索凡替尼用于非胰腺神
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—即将发表关于索凡替尼治疗非胰腺神经内分泌肿瘤患者的SANET-ep III期临床试验积极结果的最新摘要— —将于9月30日(星期一)联同试验主要研究者举行电话会议和网络音频直播,共同解
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伦敦:2019年9月18日(星期三):和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”) (AIM/Nasdaq:HCM) 将于2019年9月18-22日在中国厦门举行的第22届全国临床肿瘤学大会暨2019年CSCO学
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伦敦,2019年9月3日(星期二):和黄中国医药科技有限公司 (简称和黄医药“Chi-Med”) (AIM/Nasdaq:HCM)启动了一项HMPL-689治疗复发性或难治性淋巴瘤患者的国际I/Ib期临床试验。HMPL-689是一种作用
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伦敦 ,2019年8月23日 (星期五):和黄中国医药科技有限公司 (简称“和黄医药”或“Chi-Med”) (AIM/Nasdaq: HCM) 在中国启动了一项HMPL-523治疗免疫性血小板减少性紫癜(“ITP”)患者的I期临床试验。H
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香港:2019 年6 月14 日,周五:和黄中国医药科技有限公司(Chi-Med)(AIM/Nasdaq: HCM)今日宣布索凡替尼以晚期非胰腺神经内分泌瘤为适应症的III 期关键性研究SANET-ep 预设的中期分析已由该研
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2019年3月29日,中国上海 — 和黄中国医药科技有限公司(Chi-Med)(AIM/NASDAQ: HCM)子公司和记黄埔医药在中国启动了一项有注册性潜力的IIb/III期临床试验,旨在对比索凡替尼(HMPL-012或sulfat
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2019年3月28日,中国上海 — 和黄中国医药科技有限公司 (Chi-Med)(AIM/NASDAQ: HCM) 子公司和记黄埔医药将于2019年3月31日-4月3日在美国佐治亚州亚特兰大市召开的美国癌症研究协会(AACR)年
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香港:2019年2月12日,星期二:和黄中国医药科技有限公司 (Chi-Med)(AIM/NASDAQ: HCM)今日宣布CALYPSO II期临床研究中探索沃利替尼/Imfinzi®(durvalumab)联合疗法治疗转移性乳头状肾细胞癌(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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Press Release – FRESCO Phase III trial results for fruquintinib in colorectal cancer in an oral presentation – – Five abstracts in total accepted for fruquintinib, savolitinib and sulfatinib – London: Thursday, May 18, 2017: Hutchison Chin
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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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Press Release London: Friday, March 10, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) presented data from the ongoing Phase Ib/II clinical trial of sulfatinib in patients with advanced neuroendocrine tumors (“NET”) at
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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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