Initiation of fruquintinib Phase II study

RNS Number : 9070I

Hutchison China Meditech Limited

05 June 2014

 



Hutchison China MediTech Limited ("Chi-Med")
(AIM: HCM)

Initiation of fruquintinib Phase II study in non-small cell lung cancer

London: Thursday, 5 June 2014: Chi-Med today announces that Hutchison MediPharma Limited ("HMP"), its majority owned R&D company, has initiated a Phase II clinical trial in non-small cell lung cancer ("NSCLC") patients in China for fruquintinib (HMPL-013), its investigational small molecule agent that is designed to selectively inhibit vascular endothelial growth factor receptors ("VEGFR").  Preparations and patient screening began earlier this year, with the first patient dosed on 4 June 2014.

This randomised, double-blind, placebo-controlled, multi-centre, proof-of-concept ("POC") Phase II study is targeted at treating non-squamous NSCLC patients who have failed second-line standard chemotherapy.  This trial is to evaluate the efficacy and safety of fruquintinib versus placebo in NSCLC patients.  All patients will receive best supportive care.  The primary endpoint is progression free survival, with secondary endpoints including disease control rate, overall response rate, overall survival and safety.  Approximately 90 patients will be enrolled, with top-line results expected in 2015.

Fruquintinib is designed to selectively inhibit VEGF receptors, including VEGFR1, 2, and 3.  In the first-in-human Phase I clinical trial, 40 late-stage cancer patients were treated with fruquintinib.  Detailed results of the Phase I clinical trial were presented at the annual meeting of the American Association for Cancer Research in April 2013, and are available at http://chi-med.com/eng/irinfo/presentations.htm.  Based on the Phase I data, the first POC Phase II study was initiated on 2 April 2014, which was a randomized, double-blind, placebo-controlled, multi-centre Phase II clinical trial targeted at treating patients with locally advanced or metastatic colorectal cancer.  

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

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Enquiries

Chi-Med    Christian Hogg, CEO	Telephone:           [phone]
Panmure Gordon (UK) Limited    Richard Gray    Andrew Potts	Telephone:           [phone]
Citigate Dewe Rogerson    Anthony Carlisle    David Dible	Telephone:           [phone] Mobile:                   [phone] Mobile:                   [phone]

Notes to Editors

About vascular endothelial growth factor ("VEGF") and non-small cell lung cancer ("NSCLC") 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 thus inhibition of the VEGF/VEGFR pathway represents an exciting therapeutic strategy in blocking the development of new blood vessels essential for tumour to grow and invade.  To date, several anti-VEGF/VEGFR agents have shown clinical efficacy against a number of tumour types including colorectal, liver, breast and gastric cancer, amongst others. 

Lung cancer is the most common cancer both worldwide and in China.  The American Cancer Society estimated that about 220,000 new cases of lung cancer were diagnosed in the United States each year.  In China, lung cancer is the most commonly diagnosed cancer, with over 715,000 cases in 2012, accounting for 18.7% incidence among all cancer patients.  It is also the most common cause of cancer death.  There are two major types of lung cancer: small cell lung cancer and NSCLC.  NSCLC is a disease in which malignant cancer cells form in the tissues of the lung, and can be further classified based on cancer cell types with the most common ones including squamous cell carcinoma, large cell carcinoma and adenocarcinoma.

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

 

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