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2015 年8 月19 日星期三:和黃醫藥今日宣布收到楊森製藥( Janssen Pharmaceutical, Inc.) 關於終止HMPL-507 項目的合作研發協議的決定。 和黃醫藥與楊森製藥於2008 年開始戰略合作,並於2010 年
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For the complete release, please download the PDF. --- Drug R&D Division - our Innovation Platform: enrolling 17 clinical trials (H1 2014: 10), with 24 targeted by year-end. China Healthcare and Consumer Products Divisions - our Commercial
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London: Thursday, 23 July 2015: Hutchison China MediTech Limited ("Chi-Med") (AIM: HCM) today announces that it has signed a subscription agreement (the "Agreement") and completed the exchange of 5,247,493 convertible preference shares held by Mitsui
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London: Friday, 17 July 2015: Hutchison China MediTech Limited ("Chi-Med") (AIM: HCM) today announces that Shanghai Hutchison Pharmaceuticals Limited ("SHPL"), its prescription drug joint venture, has been granted an invention patent in China ("Inven
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London: Monday, 6 July 2015: Hutchison China MediTech Limited ("Chi-Med") (AIM: HCM) will be announcing its interim results for the six months ended 30 June 2015 on Tuesday, 28 July 2015. An analyst presentation will be held at 9:00 am on the same d
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London: Monday, 29 June 2015: Hutchison China MediTech Limited ("Chi-Med") (AIM: HCM)announces the following blocklisting six monthly return: 1. Name of applicant: Hutchison China MediTech Limited 2. Name of
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2015 年6 月1 日: 和黃醫藥今日宣布,其合作夥伴阿斯利康公佈了由和黃醫藥自主研發的c-Met 抑製劑沃利替尼(AZD6094)與阿斯利康的候選藥物AZD9291 聯合用藥治療非小細胞肺癌的Ib 期臨床
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星期二,2015 年5 月12 日:和黃中國醫藥科技有限公司今日宣布呋喹替尼以轉移性結直腸癌為適應症的首個概念驗證性(POC)臨床研究達到預期終點,成功觸發第一個里程碑,和黃醫藥將於201
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Please see http://meetinglibrary.asco.org/content/109556 The associated abstract is available at http://meetinglibrary.asco.org/content/148945-156. Meeting: 2015 ASCO Annual Meeting Session: Developmental Therapeutics – Clinical Pharmacol
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London: Thursday, 30 April 2015: For information purposes, Chi-Med hereby notifies the market that as at 30 April 2015, the issued share capital of Chi-Med consisted of 53,299,964 ordinary shares of US$1.00 each, with each share carrying one right to
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London: Friday, 24 April 2015: Chi-Med today announces that all ordinary resolutions and special resolution put to its Annual General Meeting ("AGM") held on 24 April 2015 were duly passed. Please download the PDF.  
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London: Wednesday, 22 April 2015: Chi-Med received notification on 22 April 2015 that Mr Christopher Nash, Independent Non-executive Director, has purchased 1,388 ordinary shares of US$1.00 each in Chi-Med (the “Shares”) at a price of GBP18.00 pe
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London: Thursday, 16 April 2015: Chi-Med received notification on 16 April 2015 that Simon To, Executive Director and Chairman, has purchased 28,000 ordinary shares of US$1.00 each in Chi-Med (the “Shares”) at a price of GBP15.85 per share on 15
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London: Monday, 13 April 2015: Chi-Med received notification on 13 April 2015 that Simon To, Executive Director and Chairman, has purchased 25,000 ordinary shares of US$1.00 each in Chi-Med (the “Shares”) at a price of GBP14.215 per share on 10 A
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London: Wednesday, 8 April 2015: Chi-Med received notifications on 8 April 2015 that the following Directors have purchased ordinary shares of US$1.00 each in Chi-Med (the "Shares") as follows:- Director Date of purchase
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London: Wednesday, 1 April 2015: Chi-Med announces that it has issued 64,038 ordinary shares of US$1.00 each (the "Shares") following the exercise of options by Mr Johnny Cheng, Executive Director and Chief Financial Officer of Chi-Med, at an exercis
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London: Wednesday, 1 April 2015: Chi-Med received notifications on 1 April 2015 that the following Directors have purchased ordinary shares of US$1.00 each in Chi-Med (the "Shares") as follows:- Director Date of purchase Numbe
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2015 年3 月30 日:和黃醫藥今日宣布呋喹替尼以轉移性結直腸癌為適應症的首個概念驗證性(POC)臨床研究成功達到主要試驗終點。研究結果顯示該試驗成功地達到了無進展生存期的主要療
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London: Monday, 23 March 2015: Chi-Med today announces that its 2014 Annual Report together with the Notice of Annual General Meeting and the Proxy Form have been posted to shareholders. The documents can be accessed from the website of Chi-Med (www.
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2015 年3 月6 日,週五:和黃醫藥今日宣布呋喹替尼(HMPL-013)以非小細胞肺癌為適應症的中國II 期臨床試驗完成受試者入組。呋喹替尼是和黃醫藥獨立研發的血管細胞內皮生長因子受體(V
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For the complete release, please download the PDF. -- Break-out year for Drug R&D Division with 16 clinical studies on 7 drug candidates; 10 potential Breakthrough Therapy indications; as well as record China Healthcare Division revenues and
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Press Release -  London: Thursday, 29 January 2015: Chi-Med, the pharmaceutical and healthcare company based primarily in China, today announces that Hutchison Whampoa Sinopharm Pharmaceuticals (Shanghai) Company Limited ("Hutchison Sinopharm"),
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London: Monday, 26 January 2015: Chi-Med will be announcing its final results for the year ended 31 December 2014 on Thursday, 26 February 2015. An analyst presentation will be held at 9:00 am on the same day at Citigate Dewe Rogerson, 3 London Wall
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2014年12月15日: 和黃醫藥今日宣布呋喹替尼(HMPL-013)以結直腸癌為適應症的中國III期臨床試驗(FRESCO)正式啟動。呋喹替尼是一種新型高選擇性抑制血管細胞內皮生長因子受體(VEGFR)的小
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Press Release -  London: Tuesday, 7 October 2014:  Chi-Med today announces that it will host a briefing to update analysts and investors on Hutchison MediPharma Limited (“HMP”), its majority owned pharmaceutical R&D division, in London o
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Press Release -  London: Wednesday, 1 October 2014: Chi-Med, the pharmaceutical and healthcare company based primarily in China, today announces that Chi-Med, through its subsidiary Hutchison Whampoa Sinopharm Pharmaceuticals (Shanghai) Company L
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2014 年8 月21 日: 和黃醫藥今日宣布呋喹替尼(HMPL-013)以結直腸癌為適應症的中國II 期臨床試驗完成受試者入組。呋喹替尼是一種新型高選擇性抑制血管細胞內皮生長因子受體(VEGFR)的
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2014 年8 月1 3 日:和黃醫藥與雀巢全資子公司Nestlé Health Science 組建的合資公司Nutrition Science Partners (NSP )今日公佈HMPL-004 對照安慰劑治療潰瘍性結腸炎的全球三期臨床試驗NATRUL-3 的
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2014年6月18日:和黃中國醫藥科技有限公司(簡稱 “和黃醫藥” )今日宣佈在澳洲啟動HMPL-523的I期臨床試驗。 HMPL-523是針對B細胞受體信號通路中的酪氨酸激酶Syk的新型高選擇性小分子抑制劑
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2014 年6 月5 日: 和黃中國醫藥科技有限公司(簡稱“ 和黃醫藥”)今日宣布啟動呋喹替尼(HMPL-013)以非小細胞肺癌為適應症的中國II 期臨床試驗。呋喹替尼是一種新型高選擇性抑制血管細
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2014年5月23日: 和黃中國醫藥科技有限公司(簡稱“ 和黃醫藥”)今日宣布與阿斯利康聯合啟動AZD6094 (HMPL-504/沃利替尼) (“AZD6094” )以乳頭狀腎細胞癌為適應症的全球II期臨床試驗,評估其藥
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