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CRT, CTx Work Out Cancer Deal

By Drug Discovery Trends Editor | August 21, 2012

Cancer Research Technology (CRT), the commercial arm of Cancer Research UK, is entering into two licenses with Cancer Therapeutics CRC (CTx), an Australian cancer drug and development company, to commercialize CTx’s preclinical focal adhesion kinase (FAK) inhibitor programs.

CRT, as global commercial partner of CTx, has exercised its options to take forward these two programs, which were developed by CTx, to in vivo proof-of-concept stage in mice.

The FAK inhibitor portfolio includes CTx-0294945, a highly-selective small molecule inhibitor, and CTx-0294886, a potent small molecule inhibitor of three proteins: FAK; vascular growth factor receptor 3 (VEGFR3); and FMS-like tyrosine kinase 3 (FLT3).

FAK is a non-receptor tyrosine kinase involved in controlling the growth, development and spread of different solid tumors. These include triple-negative breast cancer and merlin-negative mesothelioma, diseases which have urgent need for new treatments – and for which these molecules have potential use.

Both CTx-0294945 and CTx-0294886 separately boost the effectiveness and response length of anti-angiogenic antibody cancer drug Avastin to treat triple negative breast cancer in mice.

FAK also has an important role in controlling cancer stem cell survival, suggesting these molecules may also be able to destroy cancer stem cells.

CTx-0294886 could also be used for the treatment other cancers, including a subset of acute myeloid leukemia (AML) patients with mutations in FLT3. FLT3 is a receptor tyrosine kinase involved in controlling the growth and development of several blood cancers, including AML.

CRT is seeking to exclusively license these two programs.

Dr Phil L’Huillier, CRT’s director of business management, said: “This important partnership combines CRT’s unique global commercialisation expertise in cancer with CTx’s translational expertise, to further develop these exciting programs of potent, highly-selective and triple kinase small molecule inhibitors. These molecules have already shown promise in preclinical research to treat triple-negative breast cancer – for which there is no standard chemotherapy treatment.

“We hope that commercialization of this project will pave the way for entry into early clinical trials – leading to new adjuvant treatment options for this disease and other cancers.”

Dr Warwick Tong, CTx’s CEO, said: “We are excited that our two lead programmes have reached the stage of being actively commercialised for further development with the potential to bring significant benefits to cancer patients. That these two drug candidates could contribute in the battle to reduce tumour recurrence and spread through activity on cancer stem cells is an added bonus.

“This success recognises the benefits of a highly-focused collaborative research effort led by CTx under the Australian Government CRC program. The level of expertise and the capabilities available within our group of research partners is of the highest level; these two programs and the depth of our pipeline reflects the strength of the partnership.

“We will continue with our work translating great Australian cancer biology into new drugs for cancer patients and look forward to working with CRT to advance our programs down the development path.”

Date: August 14, 2012
Source: Cancer Research Technology


Filed Under: Drug Discovery

 

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