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Chi-Med to Announce 2020 Final Results

Press release content from Globe Newswire. The AP news staff was not involved in its creation. Chi-Med to Announce 2020 Final Results Hutchison China MediTech LimitedFebruary 3, 2021 GMT HONG KONG and SHANGHAI, China and FLORHAM PARK, N.J., Feb. 03, 2021 (GLOBE NEWSWIRE) Hutchison China MediTech Limited (“Chi-Med”) (Nasdaq/AIM: HCM) will be announcing its final results for the year ended December 31, 2020 on Thursday, March 4, 2021 at 12:00 noon Greenwich Mean Time (GMT) / 8:00 pm Hong Kong Time (HKT) / 7:00 am Eastern Standard Time (EST). Analysts and investors are invited to join a conference call and audio webcast presentation with Q&A, conducted by Chi-Med management. The conference call and audio webcast will take place at 1:00 pm GMT / 9:00 pm HKT / 8:00 am EST on Thursday, March 4, 2021 and will be webcast live via the company website at www.chi-med.com/investors/event-information/. The presentation will be available for downloading before the conference call begin

Chi-Med Initiates Rolling Submission of NDA to U S FDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors

TMCnet News Chi-Med Initiates Rolling Submission of NDA to U.S. FDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors [December 28, 2020] Chi-Med Initiates Rolling Submission of NDA to U.S. FDA for Surufatinib for the Treatment of Advanced Neuroendocrine Tumors – Company plans to complete rolling submission in the first half of 2021 – – The pivotal Phase III SANET-ep trial demonstrated surufatinib reduced risk of progression or death by 67%, extending PFS of non-pancreatic NET patients with an acceptable risk/benefit ratio – – The pivotal Phase III SANET-p trial demonstrated surufatinib reduced risk of progression or death by 51%, extending PFS of pancreatic NET patients with an acceptable risk/benefit ratio –

Chi-Med Initiates Rolling Submission of NDA to U S FDA for Surufatinib for the Treatment of

Press release content from Globe Newswire. The AP news staff was not involved in its creation. Chi-Med Initiates Rolling Submission of NDA to U.S. FDA for Surufatinib for the Treatment of . Hutchison China MediTech LimitedDecember 28, 2020 GMT – Company plans to complete rolling submission in the first half of 2021 – – The pivotal Phase III SANET-ep trial demonstrated surufatinib reduced risk of progression or death by 67%, extending PFS of non-pancreatic NET patients with an acceptable risk/benefit ratio – – The pivotal Phase III SANET-p trial demonstrated surufatinib reduced risk of progression or death by 51%, extending PFS of pancreatic NET patients with an acceptable risk/benefit ratio –

Chi-Med to Present at the 39th Annual JP Morgan Healthcare Conference – IT Business Net

Chi-Med to Present at the 39th Annual JP Morgan Healthcare Conference – IT Business Net
itbusinessnet.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from itbusinessnet.com Daily Mail and Mail on Sunday newspapers.

Investegate |Hutchison China Medi Announcements | Hutchison China Medi: Grant of Share Options under Share Option Scheme

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