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For detailed information, please visit:

http://pubs.acs.org/doi/abs/10.1021/jm500510f

 

London: Thursday, 21 August 2014: Chi-Med, today announces that Hutchison MediPharma Limited (“HMP”), its majority owned drug R&D company, has completed patient enrolment in a Phase II clinical trial of fruquintinib (HMPL-013) in colorectal cancer (“CRC”) in China.  The proof-of-concept study is investigating the efficacy and safety of fruquintinib, HMP’s investigational small molecule inhibitor of vascular endothelial growth factor receptors (“VEGFR”).

This randomised, double-blind, placebo-controlled, multi-centre, proof-of-concept Phase II study is targeted at treating patients with metastatic CRC, who have failed at least two prior chemotherapies, including fluoropyrimidine, oxaliplatin and irinotecan.  A total of 71 patients have now been randomised to receive fruquintinib plus best supportive care (“BSC”) or placebo plus BSC at a 2:1 ratio.  The primary endpoint is progression free survival, with secondary endpoints including disease control rate, overall response rate, overall survival and safety.  As a result of the rapid patient enrolment, data from this trial is expected in early 2015.

Fruquintinib is designed to selectively inhibit VEGF receptors, namely VEGFR1, VEGFR2, and VEGFR3.  In the first-in-human Phase I clinical trial 40 patients were treated with fruquintinib.  Detailed results of the Phase I clinical trial are available at http://chi-med.com/eng/irinfo/presentations.htm, and were presented at the annual meeting of the American Association for Cancer Research in April 2013.  Based on the Phase I data in CRC, a Phase Ib study was initiated which treated a further 62 CRC patients.  Detailed results of the Phase Ib clinical trial were presented at the annual meeting of the American Society of Clinical Oncology in May 2014, and also can be found at http://chi-med.com/eng/irinfo/presentations.htm.

In October 2013, HMP entered into a licensing, co-development and commercialisation agreement in China with Eli Lilly and Company for fruquintinib.

 

Ends

 

Enquiries

 

Chi-Med
Christian Hogg, CEO

Telephone:      +852 2121 8200

 

Panmure Gordon (UK) Limited Telephone:      +44 20 7886 2500
Richard Gray
Andrew Potts

 

 

 
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 vascular endothelial growth factor (“VEGF”) and colorectal cancer in China

At an advanced stage, tumours secrete large amounts of VEGF, a protein ligand, to stimulate formation of excessive vasculature (angiogenesis) around the tumour in order to provide greater blood flow, oxygen, and nutrients to the tumour.  VEGF and VEGF receptors (“VEGFRs”) play a pivotal role in tumour-related angiogenesis, and inhibition of the VEGF/VEGFR pathway therefore represents an exciting therapeutic strategy in blocking the development of new blood vessels essential for tumour to grow and invade.

Colorectal cancer is the third most commonly diagnosed cancer in China, with 10.2% incidence in 2012.  An estimated 390,000 cases of colorectal cancer were diagnosed in China.  It is the fifth most common cause of cancer death after lung, liver, stomach and oesophagus cancer.

 To date, several anti-VEGF/VEGFR agents have shown clinical efficacy against a number of tumour types.  Given the scale and growth in the China oncology market, the market for VEGF/VEGFR inhibitors in China is expected to develop quickly in the next few years.

 

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.

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.