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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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伦敦:2019年7月30日(星期二): 和黄中国医药科技有限公司(Chi-Med)(AIM /纳斯达克股票代码: HCM)今天公布截至2019年6月30日的未经审核财务数据,并公布了关键临床项目的最新进展。重点包
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London: Wednesday, July 3, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) will be announcing its interim results for the six months ended June 30, 2019 on Tuesday, July 30, 2019 at 7:00 am British Summer Time (BST) (2:00 pm
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION London: June 28, 2019: Hutchison China MediTech Limited (“
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION London: June 27, 2019: Hutchison China MediTech Limited (“
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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简称(简称“和黄医药”或 “Chi-Med”)(纳斯达克/伦敦证交所: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
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London: Wednesday, May 29, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that the ordinary resolution and special resolution put to its Extraordinary General Meeting (“EGM”) held on May 29, 2019 were dul
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London: Friday, May 3, 2019: Hutchison China MediTech Limited (“Chi-Med” or “Company”) (AIM/Nasdaq: HCM) today announces that an Extraordinary General Meeting (“EGM”) is to be held at 11:00 a.m. London time on Wednesday, May 29, 2019. An
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION Hong Kong: Monday, April 15, 2019: Hutchison China MediTech
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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(简称“和黄医药”或 “Chi-Med”)(纳斯达克/伦敦证交所:HCM)在中国启动了一项有注册性潜力的IIb/III期临床试验,旨
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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(简称“和黄医药”或 “Chi-Med”)(纳斯达克/伦敦证交所:HCM)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
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London: Thursday, March 21, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that its 2018 Annual Report together with the Notice of Annual General Meeting and the Form of Proxy have been posted to shareholders
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London: Monday, March 11, 2019: Hutchison China MediTech Limited ("Chi-Med") (AIM/Nasdaq: HCM) today published the Form 20-F for the financial year ended December 31, 2018. This is available for viewing at http://www.rns-pdf.londonstockexchange.com/r
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London: Monday, March 11, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces its audited financial results for the year ended December 31, 2018 and provides updates on key clinical programs. Video webcas
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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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London: Friday, February 8, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) will announce its final results for the year ended December 31, 2018 on Monday, March 11, 2019 at 7:00 am Greenwich Mean Time (GMT). An analyst pr
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Press Release London: Monday, January 7, 2019: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that Christian Hogg, Chief Executive Officer, will present at the 37th Annual JP Morgan Healthcare Conference on Wednes
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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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2018年11月29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”)(纳斯达克/伦敦证交所:HCM)4项合作协议,对和黄医药的索凡替尼 (surufatinib, 亦称HMPL-012或sulfatinib
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2018年11月26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”)(纳斯达克/伦敦证交所:HCM)今日宣布呋喹替尼胶囊(爱优特®)首次商业上市,并在中国开始产品销
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- 研究没有达到总生存期的主要终点,但呋喹替尼组患者无进展生存期得到延长 -   2018年11月16日,周五:和黄中国医药科技有限公司(Chi-Med(简称“和黄医药”或 “Chi-Med”)(纳斯达
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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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-呋喹替尼胶囊为转移性结直肠癌患者提供了新的口服治疗选择,将在中国市场以商品名爱优特®进行销售-   -已在JAMA发表的研究数据表明,和安慰剂相比爱优特®能够使患者总生存期得到
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London: Friday, July 27, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces its unaudited financial results for the six months ended June 30, 2018 and updates shareholders on key clinical programs. Fruquinti
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2018年7月23日:和黄中国医药科技(简称“和黄医药”或 “Chi-Med”)(纳斯达克/伦敦证交所:HCM)今日宣布在美国启动索凡替尼以胰腺神经内分泌瘤(NET)和胆管癌(BTC)为适应症的Ib/II期
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London: Friday, June 29, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) will be announcing its interim results for the six months ended June 30, 2018 on Friday, July 27, 2018 at 7:00 am British Summer Time (BST). An analy
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-继2017年ASCO年会上就FRESCO研究达到全部研究终点,呋喹替尼安全性良好,较其他靶向疗法脱靶毒性更低等数据进行口头报告后,和黄医药在2018年ASCO年会上公布了FRESCO研究进一步的研究数据-
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Press Release   London: Friday, May 11, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announced today that Christian Hogg, Chief Executive Officer, will present at the Bank of America Merrill Lynch 2018 Health Care Confe
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London: Monday, March 26, 2018: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that its 2017 Annual Report together with the Notice of Annual General Meeting and the Form of Proxy have been posted to shareholders.
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Hutchison China MediTech Limited (“Chi-Med”) Reports Final Results for the Year Ended December 31, 2017 and Updates Shareholders on Key Clinical Programs Group: Year of major progress; results in line with guidance Group revenue up 12% to $
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2018年3月6日: 和黄医药今日宣布在中国启动依吡替尼Ib/II期概念验证临床试验,目标受试者为表皮生长因子受体(EGFR)基因扩增的胶质母细胞瘤患者。胶质母细胞瘤是脑肿瘤的一种主要类型
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2018年2月13日:和黄医药今日宣布呋喹替尼(HMPL-013)以非小细胞肺癌为适应症的III期临床试验“FALUCA”顺利完成患者入组工作。呋喹替尼是一种高选择性强效口服血管内皮生长因子受体(VEGF
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2017年12月15日:和黄医药今日宣布在美国启动呋喹替尼I期桥接临床试验。呋喹替尼是一种高选择性强效口服血管内皮生长因子受体(VEGFR)1,2及3的抑制剂。呋喹替尼在中国以结直肠癌、肺癌
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2017年10月31日:和黄医药今日宣布在中国启动呋喹替尼联合紫杉醇(泰素®)以晚期胃癌或胃食管结合部(GEJ)腺癌为适应症的关键性III期临床研究,这项研究被命名为FRUTIGA 。呋喹替尼是一
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London: Monday, October 30, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announced today the closing of its underwritten public offering of American Depositary Shares ("ADSs") on the Nasdaq Global Select Market, previously
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION London: Friday, October 27, 2017: Hutchison China MediTech L
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION London: Wednesday, October 25, 2017: Hutchison China MediTec
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NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, IN OR INTO OR FROM ANY JURISDICTION WHERE TO DO SO WOULD CONSTITUTE A VIOLATION OF THE RELEVANT LAWS OF SUCH JURISDICTION London: Tuesday, October 24, 2017: Hutchison China MediTech
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–沃利替尼联合泰瑞莎®或易瑞沙®的临床研究数据于世界肺癌大会公布–   –新公布的数据有助于理解MET扩增的EGFR突变NSCLC的疾病进展过程和探索潜在的新一代治疗策略 –   2017
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– 呋喹替尼联合易瑞沙®(吉非替尼)展现出良好的疗效和安全性 –   –进一步证实呋喹替尼因其高选择性和出众的安全性而具有与其他癌症疗法相联合的巨大潜力–   2017年10月1
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2017年10月12日:和黄中国医药科技有限公司(简称“和黄医药”或“Chi-Med”)(纳斯达克/伦敦证交所:HCM)今日宣布任命莫树锦(Tony Mok)教授担任公司独立非执行董事,同时担任科学委员
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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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2017年8月29日:和黄医药今日宣布在中国启动HMPL-689的I期临床试验。HMPL-689是一种新型高选择性强效小分子抑制剂,靶向B细胞受体信号通路中的关键蛋白磷酸肌醇-3激酶δ异构体(PI3Kδ)。 此
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London: Monday, July 31, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM), the China-based biopharmaceutical company focused on discovering and developing targeted therapies for oncology and immunological diseases for the glob
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阿斯利康制药(“阿斯利康”) (LON/STO/NYSE: AZN) 和黄中国医药科技有限公司 (简称 “和黄医药”) (纳斯达克/伦敦证交所:HCM)   2017年6月29日: 和黄医药今日宣布将
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London: Thursday, June 29, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) will be announcing its interim results for the six months ended June 30, 2017 on Monday, July 31, 2017 at 7:00 am British Summer Time (BST). An ana
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2017年6月22日:和黄医药近日在中国启动HMPL-453的I/II期临床试验。HMPL-453是一种靶向成纤维细胞生长因子受体(FGFR)的新型高选择性小分子抑制剂。2017年6月19日首位受试者接受给药治疗。该
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