Pioneering new targets for drug discovery through academic-industrial partnership.
The cost and time to deliver a new medicine is now estimated to be over $2BN and 15 years, respectively, with less than 5% of drugs entering clinical trials reaching the market. The cost of these failures is huge and reducing the number of these failures has never been more important to deliver safe and affordable medicines, with the majority of conditions still having no effective therapy available. The SGC’s collaboration with pharmaceutical companies is a unique multi-institution platform for generating crucial early data and discussions to fast-track decisions around whether new discoveries are worthy of further investment and development.
There are now vast quantities of genomic information being routinely generated, but the knowhow and reagents needed to explore at the molecular level the consequences of mutation and associated knowledge to design a drug therapy are still lacking. Since 2015 the SGC’s approach has been to provide toolkits called Target Enabling Packages (TEPs) to do just this, offering the missing link between genomics and chemical biology. Some thirty of these high quality tool kits have been generated in the last four years and used internationally by researchers to catalyse their work into diverse diseases such as Fragile X syndrome, Crohn’s disease and Ewings sarcoma, and even for the development of new antibiotics. The SGC’s TEPs are leading to identification of new biology, disease understanding and ultimately innovative starting points for drug discovery.
The SGC’s work with patient groups is performed in the open with experiments being written up in real-time in web based open lab notebooks. Data and reagents are immediately publically available without restriction on use, helping to reduce the level of duplication of effort within the scientific community and wastage of resource and time.
The SGC is a global organisation, and includes sites at the Universities of Oxford and Toronto, the Karolinska Institute (Stockholm), Goethe University of Frankfurt and the University of North Carolina. With the leadership of Professor Chas Bountra OBE, the Oxford team have developed deep collaborations with Abbvie, Bayer, Boehringer Ingelheim, Janssen, Merck KGaA, MSD, Novartis, Pfizer and Takeda. Disease foundations and patients groups working with the SGC include the Genetic Alliance, Alzheimer’s Research UK, CHDI Foundation, FOP action, Myeloma UK, The Brain Tumour Charity and the Canadian FORGE initiative.
The SGC has built a unique ecosystem for collaborative research in the last 16 years producing more than 4000 publications, accelerating over 100 proprietary programmes and enabling 40 clinical projects. As such the SGC are leading innovation in early stage drug discovery to deliver projects capable of transformational changes to society.
The SGC is a registered charity (number 1097737) that receives funds from AbbVie, Bayer Pharma AG, Boehringer Ingelheim, Canada Foundation for Innovation, Eshelman Institute for Innovation, Genome Canada through Ontario Genomics Institute [OGI-055], Innovative Medicines Initiative (EU/EFPIA) [ULTRA-DD grant no. 115766], Janssen, Merck KGaA, Darmstadt, Germany, MSD, Novartis Pharma AG, Ontario Ministry of Research, Innovation and Science (MRIS), Pfizer, São Paulo Research Foundation-FAPESP, Takeda, and Wellcome.