Research update:
Breakthrough compounds for diabetes and inflammation
23 September, 2015 - C4X Discovery Holdings plc ("C4XD"), a leader in rational drug discovery and design, is pleased to provide the following research update on recent key milestones in its programmes for Type 2 diabetes and inflammation, two areas of significant unmet medical need that represent large pharmaceutical markets.
Breakthrough approach
C4XD's technology has enabled rapid progress across its programmes in recent months, providing further exciting proof-of-concept for our novel approach to drug discovery based on conformational design of solution structures. We have now met significant milestones in Type 2 diabetes and inflammation, adding to the earlier success with our Orexin-1 programme, and further demonstrating C4XD's ability to rapidly and intelligently develop new medicines for areas of high, unmet need.
C4XD expects to progress both the Type 2 diabetes and inflammation programmes into in vivo proof-of-principle testing in the next few months.
Type 2 Diabetes: targeting GPR142
C4XD has identified novel lead molecules that activate GPR142, a key factor in the production of insulin. Targeting GPR142 may stimulate insulin production in a glucose-dependent manner, avoiding the hypoglycaemia risk associated with existing diabetes therapies. GPR142 has recently become the focus of considerable research and patent activity within the pharma industry.
Using its proprietary technology, C4XD has identified critical drug design principles, enabling us to generate potent, orally available compounds in just a few months.
Inflammation
C4XD has designed novel activators for the NRF-2 pathway, which is important in mediating diseases such as Chronic Obstructive Pulmonary Disease ("COPD") and Multiple Sclerosis ("MS"). NRF-2 is the subject of considerable investment by the pharma industry; for example, it is the target for the MS drug Tecfidera®, which generated 2014 revenues of $2.9 billion.
Existing approaches activate NRF-2 in a non-specific and/or irreversible way with potential for toxic side effects. C4XD's technology has enabled us to rationally design and generate selective, reversible NRF-2 activators that may offer improved safety and efficacy.
Outlook
C4XD's most advanced compound, an oral Orexin-1 antagonist for the treatment of addiction, is in formal pre-clinical safety and toxicity studies prior to initiation of clinical trials. We expect to file a Clinical Trial Application to enable human studies at the end of 2016.
C4XD expects to be in a position to announce further news regarding novel targets in the coming weeks.
"We continue to make outstanding progress with our proprietary programmes, which are focused on areas of high unmet medical need, with large target markets" said Piers Morgan, CEO. "Our technology enables us to design novel, selective, potent leads and drug candidates in a fraction of the time and cost compared to conventional methods."
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For further information please contact:
C4X Discovery Holdings plc
Piers Morgan, CEO 07912 293832
Zeus Capital
Ross Andrews/Dan Bate 0161 831 1512
Dominic Wilson 020 7533 7727
FTI Consulting
Matthew Cole / Brett Pollard / Rob Winder / Matthew Moss 020 3727 1000
About C4XD
C4XD (AIM: C4XD) is a Manchester-based company focused on optimising drug discovery and design. It was founded in 2008 as a spin-out from the University of Manchester. The company uses its NMR-based technology to solve the dynamic 3D structures of a broad range of biomolecules, including peptides, cofactors, oligonucleotides and carbohydrates. Since C4XD's NMR technology shows what shapes active molecules prefer to adopt, it provides high-quality templates for rational drug discovery and design, and valuable conformational information for drug candidate optimisation. In addition, the data is generated faster and more reliably than standard techniques such as X-ray co-crystallography or molecular modelling. C4XD is using its technology in collaboration with the pharmaceutical industry and to build its own proprietary pipeline of high-value therapeutic candidates. For additional information please go to: www.c4xdiscovery.com