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Pin to quick picksHutchmed Regulatory News (HCM)

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Edison issues update on Hutchison China Meditech (HCM)

7 Mar 2017 11:49

Edison Investment Research Limited / Key word(s): Research Update/Final Results Edison issues update on Hutchison China Meditech (HCM) 07-March-2017 / 12:48 GMT/BST


London, UK, 07 March 2017

Edison issues ADR update on Hutchison China Meditech (HCM)

Hutchison (HCM) and partner Lilly announced positive, top-line pivotal phase III trial results for fruquintinib in 3rd line colorectal cancer. The China based FRESCO study evaluating 416 patients who had failed at least two prior chemotherapies in CRC demonstrated a clinically meaningful and statistically significant increase in both overall survival and progression-free survival compared to placebo. Consequently, HCM is preparing for a China NDA submission mid-2017; this represents the first China based oncology innovation to succeed at Phase III. We expect the full data to be presented at the 53rd American Society of Clinical Oncology Meeting (ASCO) 2 to 6 June 2017. Our valuation remains unchanged at $2.4bn.

Our SOTP valuation remains unchanged at $2.4bn ($20.1/ADS). IP is valued at $1,789m and placing the commercial platform's (CP) 2016e share of net profit on a 22.5x rating gives $657m ($5.4/ADS). Adding net cash at end June 2016 and netting out unallocated costs results in a value of $2.4bn. Approval(s), clinical data and/or deals should increase our risk-adjusted valuation.Click here to view the full report.

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Dissemination of a UK FINANCIAL NEWS, transmitted by EQS Group.The issuer is solely responsible for the content of this announcement.


End of Announcement - EQS News Service

551147 07-March-2017 

corporate-announcement transmitted by DGAP - a service of EQS Group AG.The issuer is solely responsible for the content of this announcement.

Date   Source Headline
8th May 20249:30 amRNSDirectorate Change
26th Apr 20241:30 pmRNSPositive CHMP Opinion for Fruquintinib
22nd Apr 20249:30 amRNSVesting of Awards Under the LTIP
8th Apr 20249:30 amRNS2023 Annual Report and Notice of AGM
5th Apr 20249:30 amRNSData to be Presented at AACR Congress 2024
2nd Apr 20247:00 amRNSHUTCHMED and Innovent Announce NDA Acceptance
28th Mar 20247:00 amRNSSavolitinib sNDA Accepted in China
22nd Mar 20247:00 amRNSInitiation of Registration Stage of P2/3 Trial
14th Mar 20249:00 amRNSLTIP and Share Option Scheme
5th Mar 20248:30 amRNSVesting of awards under the LTIP
28th Feb 202412:45 pmRNSPublication of Form 20-F
28th Feb 202411:30 amRNS2023 Full Year Results and Business Updates
7th Feb 20247:00 amRNSPresentation of Phase III Data on Fruquintinib
2nd Feb 20248:37 amRNSInmagene Exercises Option for Two Drug Candidates
1st Feb 20248:30 amRNSHUTCHMED to Announce 2023 Final Results
30th Jan 20247:12 amRNSHUTCHMED Receives Marketing Approval in Hong Kong
11th Jan 20247:00 amRNSSovleplenib NDA Granted Priority Review in China
29th Dec 20238:30 amRNSTotal Voting Rights
29th Dec 20238:30 amRNSBlocklisting Six Monthly Return
21st Dec 202310:00 amRNSOverseas Regulatory Announcement
13th Dec 20237:00 amRNSInclusion in National Reimbursement Drug List
13th Dec 20237:00 amRNSCompleted Enrollment of Phase II/III Trial
7th Dec 202310:04 amRNSOverseas Regulatory Announcement
1st Dec 20237:00 amRNSClinical Data to be Presented at Congresses
30th Nov 20238:30 amRNSTotal Voting Rights
9th Nov 20237:00 amRNSU.S. FDA Approval of FRUZAQLAâ„¢ (fruquintinib)
24th Oct 20239:30 amRNSVesting of awards under the LTIP
16th Oct 20239:30 amRNSClinical Data to be Presented at ESMO 2023
29th Sep 20239:30 amRNSNDA Submission for Fruquintinib in Japan
29th Sep 20239:30 amRNSTotal Voting Rights
14th Sep 20239:30 amRNSDirector’s Share Dealing
12th Sep 20239:30 amRNSPhase IIIb Savolitinib Results at WCLC 2023
12th Sep 20237:00 amRNSPatient Enrollment Completed for Bridging Study
31st Aug 20239:30 amRNSTotal Voting Rights
29th Aug 20237:00 amRNSBTD in China for Savolitinib for Gastric Cancer
21st Aug 20237:00 amRNSSovleplenib Phase 3 Study Meets Primary Endpoint
7th Aug 20239:30 amRNSExercise of Share Options by a Director
31st Jul 202312:00 pmRNSInterim Results and Business Updates
20th Jul 20237:00 amRNSBreakthrough Therapy Designation for Fruquintinib
13th Jul 20239:30 amRNSChanges to Board and Technical Committee
10th Jul 20237:00 amRNSPhase 1 Study of HMPL-415 Initiated
29th Jun 20239:30 amRNSBlocklisting Six Monthly Return
26th Jun 20239:30 amRNSHUTCHMED to Announce 2023 Half-Year Results
16th Jun 20237:00 amRNSPhase III FRESCO-2 Results in The Lancet
15th Jun 20233:39 pmRNSMAA of Fruquintinib Validated by the EMA
9th Jun 202310:30 amRNSHUTCHMED Highlights Presentations at EHA and ICML
6th Jun 202310:00 amRNSLTIP and Share Option Scheme
31st May 20239:30 amRNSTotal Voting Rights
26th May 20237:00 amRNSFruquintinib NDA Granted Priority Review by FDA
26th May 20237:00 amRNSHUTCHMED Highlights Presentations at ASCO 2023

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