Less Ads, More Data, More Tools Register for FREE

Pin to quick picksHutchmed Regulatory News (HCM)

Share Price Information for Hutchmed (HCM)

Share Price is delayed by 15 minutes
Get Live Data
161.50    -11.00 (-6.38%)
Bid:
158.50
Ask:
162.50
Spread: 4.00 (2.524%)
Market Cap: £1.39b
HCM Live PriceLast checked at - London Stock Exchange

Intraday Hutchmed Share Chart

HMPL-004 Interim Analysis

13 Aug 2014 07:00

RNS Number : 9920O
Hutchison China Meditech Limited
13 August 2014
 



Hutchison China MediTech Limited ("Chi-Med")

(AIM: HCM)

 

HMPL-004 NATRUL-3 interim analysis result

 

London: Wednesday, 13 August 2014: Nutrition Science Partners Limited ("NSP"), a 50/50 joint venture between Chi-Med and Nestlé Health Science SA, today announces that a planned interim analysis was conducted on NATRUL-3, the global Phase III induction trial of HMPL-004 vs. placebo in ulcerative colitis. An independent Data Safety and Monitoring Committee ("DSMC") evaluated the unblinded data of two doses of HMPL-004 vs. placebo, and has recommended that NSP terminate the study. No meaningful safety signals or risks for patients were identified, and further analysis and review of the data will be conducted. The NSP Board will continue to evaluate the potential opportunities of HMPL-004 in new indication areas and alternative regulatory pathways.

 

Ends

Enquiries

Chi-Med

Christian Hogg, CEO

 

Telephone: +852 2121 8200

Panmure Gordon (UK) Limited

Richard Gray

Andrew Potts

 

Telephone: +44 20 7886 2500

Citigate Dewe Rogerson

Anthony Carlisle

David Dible

Telephone: +44 20 7638 9571

Mobile: +44 7973 611 888

Mobile: +44 7967 566 919

 

 

Notes to Editors

About NATRUL

NATRUL is the Phase III registration trial programme designed to evaluate the efficacy and safety of HMPL-004 in patients with mild-to-moderate UC. The first study, NATRUL-3, enrolled and treated its first patient in April 2013. Its primary endpoint is to evaluate treatments of HMPL-004 compared with placebo in patients with active UC who have an inadequate response to their current treatment with Mesalamine. The second study, NATRUL-4, is designed to evaluate HMPL-004 as a 52-week maintenance therapy. Subjects who have completed NATRUL-3 are eligible to enter NATRUL-4 directly.

 

About Nutrition Science Partners

Nutrition Science Partners ("NSP") is focused on researching, developing, manufacturing and marketing worldwide novel medicines and nutritional products derived from botanical plant origins. NSP focuses on gastrointestinal indications, and may in the future expand into the metabolic disease and brain health areas. NSP is a 50/50 joint venture formed by Nestlé Health Science and Chi-Med. 

 

About Nestlé Health Science

Nestlé Health Science, a wholly-owned subsidiary of Nestlé, has an ever developing innovative portfolio of nutritional therapies, supported variously by proprietary diagnostics and devices, targeted towards the Vital Support areas of aging and critical/intensive care, as well as Gastrointestinal, Brain, Metabolic and Consumer Health, changing the way patients and healthcare professionals approach the management of health. Nestlé Health Science employs around 3,500 people worldwide and has its headquarters in Vevey, Switzerland. For more information, please visit www.nestlehealthscience.com. 

 

 

About HMP

HMP is a novel drug R&D company focusing on discovering, developing and commercialising innovative therapeutics in oncology and autoimmune diseases. With a team of around 200 scientists and staff, its pipeline is comprised of novel oral compounds for cancer and inflammation in development in North America, Europe, Australia and Greater China.

 

HMP is majority owned by Chi-Med. For more information, please visit: www.hmplglobal.com.

 

 

About Chi-Med

Chi-Med is a China-based healthcare group focused on researching, developing, manufacturing and selling pharmaceuticals and health-related consumer products. Its China Healthcare Division manufactures, markets and distributes prescription and over-the-counter pharmaceuticals in China. Its Drug R&D Division focuses on discovering and developing innovative therapeutics in oncology and autoimmune diseases. Its emerging Consumer Products Division focuses on organic and natural consumer products in Asia.

 

Chi-Med is majority owned by the multinational conglomerate Hutchison Whampoa Limited (SEHK:13). For more information, please visit: www.chi-med.com.

This information is provided by RNS
The company news service from the London Stock Exchange
 
END
 
 
MSCEXLBFZVFEBBD
Date   Source Headline
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 amRNSHUTCHMED Highlights Presentations at ASCO 2023
26th May 20237:00 amRNSFruquintinib NDA Granted Priority Review by FDA
17th May 20239:30 amRNSStandard form for notification of major holdings
12th May 20231:15 pmRNSAnnual General Meeting Poll Results
12th May 20239:30 amRNSBoard of Directors and Board Committee Membership
10th May 20239:30 amRNSAppointment of Independent NED
28th Apr 20239:30 amRNSTotal Voting Rights
21st Apr 20239:30 amRNSVesting of awards under the LTIP
18th Apr 20237:00 amRNSNDA Acceptance in China for Fruquintinib
12th Apr 20237:00 amRNSPresentations at AACR Annual Meeting 2023
11th Apr 20239:30 amRNS2022 Annual Report and Notice of AGM
11th Apr 20239:30 amRNSIntended Retirement of Independent NED
4th Apr 202310:30 amRNSHUTCHMED Initiates Registration Phase Enrollments
31st Mar 20239:30 amRNSTotal Voting Rights
31st Mar 20237:00 amRNSRolling Submission of Fruquintinib US NDA Complete
14th Mar 20231:30 pmRNSClosing of Fruquintinib License to Takeda
8th Mar 20238:30 amRNSDirector's Share Dealing
6th Mar 20238:30 amRNSVesting of awards under the LTIP
28th Feb 202312:15 pmRNSPublication of Form 20-F
28th Feb 20238:30 amRNS2022 Full Year Results and Business Updates
27th Feb 202310:00 amRNSEnrollment Completed in Phase 2 Amdizalisib trial
31st Jan 20238:30 amRNSNotice of Results
23rd Jan 20238:00 amRNSLicense to Takeda for Fruquintinib outside China
18th Jan 20232:30 pmRNSInclusion of ORPATHYS in NRDL in China
3rd Jan 20238:30 amRNSEnrollment Completed in Phase 3 Trial
30th Dec 20228:30 amRNSBlocklisting Six Monthly Return
19th Dec 202210:00 amRNSFDA NDA Rolling Submission for Fruquintinib
15th Nov 20227:00 amRNSHUTCHMED Announces Strategy Update
14th Nov 20227:00 amRNSPositive Topline Phase 3 Result in Fruquintinib
27th Oct 202212:30 pmRNSHUTCHMED Initiates Phase 2/3 Trial of Fruquintinib
21st Oct 20229:30 amRNSVesting of awards under the LTIP
10th Oct 20229:30 amRNSPhase II/III Trial of Sovleplenib for in China
30th Sep 20229:30 amRNSTotal Voting Rights
14th Sep 202211:00 amRNSShare Option Scheme and Long Term Incentive Plan
8th Sep 20227:00 amRNSFRESCO-2 Colorectal Cancer MRCT Data Highlights
23rd Aug 202210:00 amRNSHolding(s) in Company
23rd Aug 20229:30 amRNSHUTCHMED To Present FRESCO-2 Data at ESMO 2022
9th Aug 20229:30 amRNSFirst Participant in Phase I Trial of IMG-004
8th Aug 20229:30 amRNSPreliminary results from SAVANNAH Phase 2 Trial
8th Aug 20227:00 amRNSFRESCO-2 Study Has Met Primary Endpoint
1st Aug 202212:04 pmRNSInterim Results and Business Updates
1st Aug 20227:00 amRNSHUTCHMED Initiates Bridging Study of Tazemetostat
15th Jul 20229:30 amRNSHUTCHMED Initiates Phase I Trial of HMPL-A83
13th Jul 20227:00 amRNSResults of SAVANNAH Global Phase II Trial at WCLC
6th Jul 20227:00 amRNSFirst Participants in Phase I Trial of IMG-007
30th Jun 20229:30 amRNSTotal Voting Rights

Due to London Stock Exchange licensing terms, we stipulate that you must be a private investor. We apologise for the inconvenience.

To access our Live RNS you must confirm you are a private investor by using the button below.