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公告及新闻稿, 集团 | 2018-03-12

Publication of Form 20-F for the Year Ended December 31, 2017
公告及新闻稿, 集团 | 2018-03-12

Chi-Med Reports Final Results for the Year Ended December 31, 2017 and Updates Shareholders on Key Clinical Programs
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2018-03-06

和黄医药在中国启动依吡替尼以胶质母细胞瘤为适应症的Ib/II期概念验证临床试验
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2018-02-13

和黄医药完成呋喹替尼以非小细胞肺癌为适应症的III期临床试验的患者入组工作，共招募527名患者
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-12-15

和黄医药在美国启动呋喹替尼临床试验
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-10-31

和黄医药启动呋喹替尼以二线胃癌为适应症的III期临床研究FRUTIGA
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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公告及新闻稿, 集团 | 2017-10-30

Chi-Med Announces the Closing of U.S. Public Offering of American Depositary Shares (ADSs) Raising Approximately US$301.3 Million on the Nasdaq Global Select Market
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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公告及新闻稿, 集团 | 2017-10-27

Chi-Med Announces the Full Exercise of Underwriters' Over-allotment Option
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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公告及新闻稿, 集团 | 2017-10-26

Chi-Med Announces Pricing of U.S. Public Offering of ADSs Raising US$262 Million on Nasdaq Global Select Market (RNS)
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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新闻稿, 集团 | 2017-10-26

Chi-Med Announces Pricing of U.S. Public Offering of ADSs Raising US$262 Million on Nasdaq Global Select Market
London: Wednesday, October 25, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announced today the pricing of the underwritten public offering previously announced by Chi-Med on October 24, 2017. Chi-Med will issue and sell 9
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公告及新闻稿, 集团 | 2017-10-25

Chi-Med Announces Proposed Offering of ADSs (RNS)
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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新闻稿, 集团 | 2017-10-24

Chi-Med Announces Proposed Offering of ADSs
London: Tuesday, October 24, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announced today that it intends to offer, subject to market and other conditions, US$262.0 million of American Depositary Shares (“ADSs”), each
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-10-17

和黄医药联合阿斯利康开发的沃利替尼二线治疗MET扩增的EGFR突变肺癌患者展现出良好的临床抗肿瘤活性
–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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-10-16

和黄医药公布呋喹替尼联合疗法用于肺癌一线治疗的II期临床研究初步结果
– 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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公告及新闻稿, 新闻稿, 集团 | 2017-10-12

和黄医药董事会董事任命
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-09-29

Chi-Med Highlights Oral Presentations at CSCO Annual Meeting
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-09-29

Chi-Med to Present Savolitinib and Fruquintinib Clinical Data at WCLC 2017 Annual Meeting
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-08-29

和黄医药在中国启动高选择性PI3Kδ抑制剂HMPL-689以淋巴瘤为适应症的I期临床试验
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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公告及新闻稿, 集团 | 2017-07-31

Chi-Med Reports 2017 Interim Results and Updates Shareholders on Key Clinical Programs
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-06-29

和黄医药与阿斯利康联手启动沃利替尼治疗乳头状肾细胞癌的全球III期临床试验“SAVOIR”
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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公告及新闻稿, 新闻稿, 集团 | 2017-06-29

Chi-Med to Announce 2017 Half-Year Financial Results
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-06-22

和黄医药在中国启动新型FGFR抑制剂HMPL 453的I/II期临床试验
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-06-12

和黄医药向国家食品药品监督管理局递交呋喹替尼治疗晚期结直肠癌的新药上市申请
  –国家食品药品监督管理局已受理申请，并将由 药品审评中心作技术审核– –将收到来自礼来共计3080万人民币的里程碑付款–   2017年6月12日：和黄医药今日宣布药物呋喹替尼
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-06-05

和黄医药在ASCO年会上就呋喹替尼临床III期研究数据进行口头报告
2017年6月5日：和黄医药宣布在今天于美国芝加哥举行的美国临床肿瘤学会（ASCO）年会上就其自主研发的高选择性血管细胞内皮生长因子受体（VEGFR）抑制剂的关键III期临床研究结果进行了口
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-05-18

和黄医药在ASCO 2017年会上公布临床数据
  – 受ASCO组委会邀请口头报告呋喹替尼治疗结直肠癌的III期临床研究“FRESCO”的研究结果 –   –将在大会上展示呋喹替尼，沃利替尼和索凡替尼共5项研究摘要 –   2017年5月18
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-04-07

和黄医药在2017年AACR年会上公布呋喹替尼和索凡替尼的临床前数据
2017年4月7日：和黄医药在2017年4月1日至5日于美国华盛顿举行的美国癌症研究协会(AACR)年会上公布了呋喹替尼和索凡替尼的临床前数据。呋喹替尼和索凡替尼目前都在以多种癌症为适应症的III
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公告及新闻稿, 集团 | 2017-03-27

2016 Annual Report and Notice of Annual General Meeting
London: Monday, March 27, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that its 2016 Annual Report together with the Notice of Annual General Meeting and the Form of Proxy have been posted to shareholders.
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公告及新闻稿, 新闻稿, 集团 | 2017-03-24

Chi-Med Appoints Weiguo Su, Chief Scientific Officer, to Board of Directors
Appointment of Director London: Friday, March 24, 2017: Hutchison China MediTech Limited (“Chi-Med” or the “Company”) (AIM/Nasdaq: HCM) today announces that Dr Weiguo Su has been appointed as Executive Director and member of Technical Commi
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-03-21

Chi-Med to host R&D Briefings on March 29 & 30, 2017
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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公告及新闻稿, 新闻稿, 集团 | 2017-03-16

Grant of Awards under Long Term Incentive Plan
Press Release London: Thursday, March 16, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) announces that on March 15, 2017, it granted conditional awards (“LTIP Awards”) under the Long Term Incentive Plan (“LTIP”) a
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公告及新闻稿, 集团 | 2017-03-13

Publication of Form 20-F for the Year Ended December 31, 2016
London: Monday, March 13, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today published the Form 20-F for the financial year ended December 31, 2016 per attached and also available for viewing on the Company's website at ww
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公告及新闻稿, 集团 | 2017-03-13

Chi-Med Reports Final Results for the Year Ended December 31, 2016 and Updates on Key Clinical Programs
Hutchison China MediTech Limited (“Chi-Med”) Reports Final Results for the Year Ended December 31, 2016 and Updates Shareholders on Key Clinical Programs Group: Record revenue, net income and clinical investment in 2016 Group revenue up 21%
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-03-10

和黄医药在欧洲神经内分泌肿瘤学会年会上公布索凡替尼治疗神经内分泌瘤Ib/II期临床试验结果
2017年3月10日：和黄医药在2017年3月8日至10日于西班牙巴塞罗那举行的第14届欧洲神经内分泌肿瘤学会年会（ENETS）上公布了索凡替尼正在进行的治疗晚期神经内分泌瘤的Ib/II期临床试验结果。
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公告及新闻稿, 肿瘤学 / 免疫学 | 2017-03-03

和黄医药宣布呋喹替尼（HMPL-013）以局部晚期或转移性结直肠癌为适应症的III期临床试验“FRESCO”取得成功
  –达到首要和次要终点 – – 安全性及疗效达到预期 – –计划于2017年中递交中国新药上市申请– –完整详细的试验结果将在2017年中通过肿瘤学术大会公布–   2017年3月3日：
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公告及新闻稿, 新闻稿, 集团 | 2017-02-28

Chi-Med Appoints Graeme Jack as Independent Non-executive Director and Chairman of Audit Committee
Change of Directors London: Tuesday, February 28, 2017: Hutchison China MediTech Limited (“Chi-Med” or the “Company”) (AIM/Nasdaq: HCM) today announces that with effect from March 1, 2017:- Mr Graeme Allan Jack has been appointed as I
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-02-20

Chi-Med Initiates a Phase II Study of Savolitinib in Pulmonary Sarcomatoid Carcinoma
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-02-14

Chi-Med Initiates First-In-Human Clinical Trial of Novel FGFR Inhibitor HMPL-453 in Australia
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-02-14

Chi-Med and AstraZeneca Present Savolitinib Papillary Renal Cell Carcinoma Phase II Results at 2017 Genitourinary Cancers Symposium
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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公告及新闻稿, 新闻稿, 集团 | 2017-02-01

Chi-Med Appoints Industry Veteran Karen Ferrante to Board of Directors
Change of Directors London: Wednesday, February 1, 2017: Hutchison China MediTech Limited ("Chi-Med") (AIM/Nasdaq: HCM) today announces that with effect from today:- Dr Karen Jean Ferrante has been appointed as Independent Non-Executive Director
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公告及新闻稿, 新闻稿, 集团 | 2017-01-16

Chi-Med Appoints Industry Veteran Paul Carter to Board of Directors
Change of Directors London: Monday, January 16, 2017: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces with effect from February 1, 2017, Mr Paul Rutherford Carter has been appointed as Senior Independent Non-Execut
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-01-16

Chi-Med Initiates a Phase II Combination Study of Fruquintinib with Iressa® (gefitinib) in First-Line Non-Small Cell Lung Cancer
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-01-16

Chi-Med Initiates a Phase II Study of Sulfatinib in Second-line Biliary Tract Cancer in China
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-01-16

Chi-Med Presents Phase I/II Clinical Data for Selective VEGFR Inhibitor Fruquintinib at the 2017 Gastrointestinal Cancers Symposium
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2017-01-10

Chi-Med Initiates HMPL-523 Clinical Trials in Hematological Cancer in China
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2016-12-06

Chi-Med Presents Pre-clinical Data for Selective Syk Inhibitor HMPL-523 at the 2016 American Society of Hematology Annual Meeting
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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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2016-11-23

Chi-Med to Present Data from Proof-of-Concept Clinical Trials for Fruquintinib and Epitinib at the 17th World Conference on Lung Cancer (“WCLC”)
Press Release London: Wednesday, November 23, 2016: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that results from two non-small cell lung cancer (“NSCLC”) clinical studies will be presented at WCLC in Vienn
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公告及新闻稿, 新闻稿, 肿瘤学 / 免疫学 | 2016-11-14

Chi-Med Presents Phase I Clinical Data for Selective Syk Inhibitor HMPL-523 at the 2016 ACR/ARHP Annual Meeting
Press Release London: Monday, November 14, 2016: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces that data from a recent Phase I, first-in-human, dose escalating study of the safety, tolerability and pharmacokineti
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公告及新闻稿, 其他业务, 新闻稿 | 2016-10-31

Chi-Med Commercial Platform Joint Venture Receives US$59.5 Million Land Compensation Payment
Shanghai agreement triggers a one-time gain to Chi-Med of US$38.2 million in Q4 2016 Shanghai factory relocation complete: now operational with three-fold increase in capacity Cash from Chi-Med Commercial Platform supports developmen
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公告及新闻稿, 集团 | 2016-08-02

Change of Non-executive Directors
London: Tuesday, August 2, 2016: Hutchison China MediTech Limited (“Chi-Med”) (AIM/Nasdaq: HCM) today announces with effect from August 1, 2016, Dr Dan Eldar has been appointed as a Non-Executive Director of Chi-Med in place of Mr Salbaing who ha
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公告及新闻稿, 集团 | 2016-08-02

Chi-Med Reports Interim Results for the Six Months Ended June 30, 2016, Provides 2016 Financial Guidance and Updates Shareholders on Key Clinical Programs
Group revenue up 27% to $104.5 million (H1 2015: $82.5m) and net income attributable to Chi‑Med of $0.5 million (H1 2015: $15.9m), reflecting a sharp increase in clinical investment.   Innovation Platform – Seven drug candidates in 25
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